The Vespiary

The Hive => Novel Discourse => Topic started by: Rhodium on March 19, 2004, 08:46:00 AM

Title: Archive of "Wanted References" Volume 1
Post by: Rhodium on March 19, 2004, 08:46:00 AM
The thread

Post 217986 (https://www.thevespiary.org/talk/index.php?topic=11962.msg21798600#msg21798600)

(Rhodium: "Wanted references", Novel Discourse)
in this forum for requesting journal articles which are out of reach for yourself often becomes cluttered with posts after a while (so that it is hard to see which articles are still wanted and which has been retrieved), and as it is a waste to just delete the posts containing links to the retrieved articles (other bees than the actual requester may find them interesting), I will from now on collect these links in this separate digest (sorted according to who retrieved them) one week after they were first posted in

Post 217986 (https://www.thevespiary.org/talk/index.php?topic=11962.msg21798600#msg21798600)

(Rhodium: "Wanted references", Novel Discourse)
.

This Digest only covers articles posted in March 2004 or earlier. For articles posted in April 2004 or later, please refer to

Post 499541 (https://www.thevespiary.org/talk/index.php?topic=11630.msg49954100#msg49954100)

(Rhodium: "Archive of "Wanted References" Volume 2", Novel Discourse)


Please PM me if any of the links below expire, so that I can remove them from this list.



Retrieved by Chimimanie:

For Lego: (copy and paste them because the link dont work):
Synthesis of psilocine from N, N-dimethyltryptamine
Comptes Rendus des Seances de l'Academie des Sciences, Serie C:  Sciences Chimiques  (1969),  269(1),  51-3

http://members.lycos.co.uk/chimimanie/C%20R%20Acad%20Sci%20269%20%281969%29%20C%2051.PDF (http://members.lycos.co.uk/chimimanie/C%20R%20Acad%20Sci%20269%20%281969%29%20C%2051.PDF)


http://members.lycos.co.uk/chimimanie/C%20R%20Acad%20Sci%20275%20%281972%29%20C%20613.PDF (http://members.lycos.co.uk/chimimanie/C%20R%20Acad%20Sci%20275%20%281972%29%20C%20613.PDF)


http://members.lycos.co.uk/chimimanie/indole%20thio%20amide.PDF (http://members.lycos.co.uk/chimimanie/indole%20thio%20amide.PDF)



For Kinetic:

http://members.lycos.co.uk/chimimanie/chlorodifluoromethane.pdf (http://members.lycos.co.uk/chimimanie/chlorodifluoromethane.pdf)



For Rhodium:
2,5-Dimethoxyallylbenzene isomerization with PdCl2(MeCN)2
Aust. J. Chem. 43, 777-781 (1990)

http://members.lycos.co.uk/chimimanie/austjchem-777-1990.PDF (http://members.lycos.co.uk/chimimanie/austjchem-777-1990.PDF)



Synthesis of Methadone
Bull. Soc. Chim. Belg. 90(9), 977-82 (1981)

http://members.lycos.co.uk/chimimanie/BSCBelg977-1981.PDF (http://members.lycos.co.uk/chimimanie/BSCBelg977-1981.PDF)



For Vitus_Verdegast:
5-iodo-2-aminoindan, a non-neurotoxic analogue of p-iodo-amphetamine
Nichols, D.E.; Johnson, M.P. and Oberlender, P.

Pharmacol. Biochem. Behav. 38, 1, p.135 (1991) (https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-nonneurotoxic.5.iodo-2-aminoindane.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-nonneurotoxic.5.iodo-2-aminoindane.pdf)
DOI:

10.1016/0091-3057(91)90601-W (http://dx.doi.org/10.1016/0091%2D3057%2891%2990601%2DW)



And BTW Here is the ref requested by Dr Shulgin in TiHKAL #30:
Salutations Mr Shulgin :)

http://members.lycos.co.uk/chimimanie/Bull%20Soc%20Chim%20Fr%201965%205%201417%20.PDF (http://members.lycos.co.uk/chimimanie/Bull%20Soc%20Chim%20Fr%201965%205%201417%20.PDF)






Retrieved by Rhodium:

For roger2003:
Zur Kenntnis der Glyoxylsäure
Hans Meyer

Chem. Ber. 34, 3593-93 (1904) (https://www.thevespiary.org/rhodium/Rhodium/pdf/glyoxylic.ber.37.3592.1904.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/glyoxylic.ber.37.3592.1904.pdf)

For pHarmacist:
Deveral Derivatives of p-Chlorophenoxyacetic Acid
N. A. Zakharova, et al.

Chemical Abstracts, Vol 63, 17948 (1965) (https://www.thevespiary.org/rhodium/Rhodium/pdf/p-chlorophenoxyacetic.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/p-chlorophenoxyacetic.pdf)
(Unfortunately I believe that you will have to make do with only the abstract - Rumor says that odd journal is only kept in a total of five libraries in the western world...)

For Merbst:
Synthesis and Biological Evaluation of 14-Alkoxymorphinans. 8. 14-Methoxymetopon, an Extremely Potent Opioid Agonist
H. Schmidhammer, A. Schratz, J. Mitterdorfer

Helv. Chim. Acta.  73, 1784-87 (1990) (https://www.thevespiary.org/rhodium/Rhodium/pdf/14-methoxymetopon.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/14-methoxymetopon.pdf)

For Lego:
S-Oxidation products of alkylthioamphetamines
Rezende, Marcos Caroli; Nunez, Christian; Sepulveda-Boza, Silvia; Cassels, Bruce K.; Hurtado-Guzman, Claudio.

Synthetic Communications 32(17), 2741-2750 (2002) (https://www.thevespiary.org/rhodium/Rhodium/pdf/aleph-2.4-mta.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/aleph-2.4-mta.pdf)

Bromodecarbonylation and Bromodecarboxylation of Electron-Rich Benzaldehydes and Benzoic Acids with Oxone® and Sodium Bromide
Bon-Suk Koo; Eun-Hoo Kim; Kee-Jung Lee

Synthetic Communications 32(15), 2275-2286 (2002) (https://www.thevespiary.org/rhodium/Rhodium/pdf/bromodecarbo_ylation.nabr-oxone.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/bromodecarbo_ylation.nabr-oxone.pdf)
DOI:

10.1081/SCC-120005997 (http://dx.doi.org/10.1081/SCC%2D120005997)



Alkylation of alkyl nitroacetates under PTC conditions    
Gogte, V. N.; Natu, A. A.; Pore, V. S.

Synthetic Communications 17(12),  1421-9 (1987) (https://www.thevespiary.org/rhodium/Rhodium/pdf/nitroacetate.ptc.alkylation.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nitroacetate.ptc.alkylation.pdf)
Abstract: Treatment of O2NCHRCO2R1 (I; R = H, R1 = Me; R = Me, R1 = Et) with p-R2C6H4CH2Br (R2 = H, Cl, MeO) and KHCO3 in DMF contg. TEBA gave 70-78% p-R2C6H4CH2CR(NO2)CO2R1.  Similar treatment of I (R = H, R1 = Me) with p-O2NC6H4CH2Br gave (p-NO2C6H4CH2)2C(NO2)CO2Me.

In situ reagents for thionation of amides, peptides and lactams
Dennis Brillon

Synthetic Communications 20(19), 3085-3095 (1990) (https://www.thevespiary.org/rhodium/Rhodium/pdf/amide-thionation.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/amide-thionation.pdf)
Abstract: An agent, prepd. from 1:1 P2S5 and Na2CO3 in situ, is used for thionation of amides, amino acids, peptides, and lactams.  Yields range from 28 to 96%.
As mentioned in:

Post 468717 (https://www.thevespiary.org/talk/index.php?topic=12405.msg46871700#msg46871700)

(Lego: "Amide to thioamide to amine", Serious Chemistry)


For Aurelius:
Direct Conversions of Ethers to Esters by Trichloroisocyanuric Acid

Tet. Lett. 55, 5819-5820 (1968) (https://www.thevespiary.org/rhodium/Rhodium/pdf/ethers2esters.trichloroisocyanuric.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/ethers2esters.trichloroisocyanuric.pdf)

The Oxidation of Alcohols and Ethers Using Calcium Hypochlorite [ Ca(OCl)2 ]

Tet. Lett. 23(1), 35-38 (1982) (https://www.thevespiary.org/rhodium/Rhodium/pdf/roh-ror2esters.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/roh-ror2esters.pdf)

Oxidation Studies of Symmetrical and Unsymmetriclal Ethers - Comparison of Trichloroisocyanuric Acid and Hypochlorous Acid

Tetrahedron 27, 2671-2674 (1971) (https://www.thevespiary.org/rhodium/Rhodium/pdf/ether-oxidation.tica-hocl.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/ether-oxidation.tica-hocl.pdf)

Allylbenzenes by Friedel-Craft alkylation with Allyl Alcohol, catalyzed by K-10 Acidic Clay

J. Chem. Soc. Perkin Trans 1, 3519-3520 (1994) (https://www.thevespiary.org/rhodium/Rhodium/pdf/fc-alkylation.k10-clay.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/fc-alkylation.k10-clay.pdf)

For Twodogs:

J. Chem. Educ. 76, 1717 (1999) (https://www.thevespiary.org/rhodium/Rhodium/pdf/hofmann-bleach.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/hofmann-bleach.pdf)

For Vitus_Verdegast:

Org. Proc. Res. Dev. 4, 534-543 (2000) (https://www.thevespiary.org/rhodium/Rhodium/pdf/md-mandelic2piperonal.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/md-mandelic2piperonal.pdf)
(And if you look around you will find sections of this already posted here)

For Antoncho:

Haworth and Lapworth, J. Chem. Soc., 121, 76 (1922) (https://www.thevespiary.org/rhodium/Rhodium/djvu/acetalization.aldehydes.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/acetalization.aldehydes.djvu)

For Captain_Mission:
Direct conversion of Bromohydrins to ketones by a free radical elimination of HBr

J. Org. Chem. Vol. 67(1), 312-313(2002) (https://www.thevespiary.org/rhodium/Rhodium/pdf/bromohydrin2ketone.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/bromohydrin2ketone.pdf)

Simple, inexpensive procedure for the large-scale production of alkyl quinones

J. Org. Chem.; 1983; 48(17); 2932-2933.  (https://www.thevespiary.org/rhodium/Rhodium/pdf/large-scale.alkyl-quinones.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/large-scale.alkyl-quinones.pdf)

For Ganesha:
Amphetamine Analogs. II. Methylated Phenethylamines later addition (03-15-04):
Beng T. Ho, et. al.

J. Med. Chem. 13, 134-135 (1970) (https://www.thevespiary.org/rhodium/Rhodium/pdf/amph-analog-2.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/amph-analog-2.pdf)

Psychotropic Phenylisopropylamines derived from Apiole and Dillapiole later addition (03-15-04):
Alexander T. Shulgin

Nature 215, 1494-95 (1967) (https://www.thevespiary.org/rhodium/Rhodium/chemistry/dmmda.shulgin.html)

(https://www.thevespiary.org/rhodium/Rhodium/chemistry/dmmda.shulgin.html)

Structure-Activity Relationships of One-Ring Psychotomimetics later addition (03-15-04):
Alexander T. Shulgin, Thornton Sargent, Claudio Naranjo

Nature 221, 537-541 (1969) (https://www.thevespiary.org/rhodium/Rhodium/djvu/shulgins.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/shulgins.djvu)

For Chimimanie:
The Alkaloids, Vol III:

https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.vol3.ch22.pea.pdf (https://www.thevespiary.org/rhodium/Rhodium/pdf/the.alkaloids.vol3.ch22.pea.pdf)



Acta Pharm. Suecia 16, 267-270 (1979)

https://www.thevespiary.org/rhodium/Rhodium/chemistry/mescaline.html (https://www.thevespiary.org/rhodium/Rhodium/chemistry/mescaline.html)

(Under the heading "A Novel Route for the Synthesis of Mescaline")

The use of nitrilium salts in the synthesis of heterocyclic compounds. I. Derivatives of 3,4-dihydroisoquinoline
Lora-Tamayo, Manuel; Madronero, Ramon; Munoz, Guillermo Garcia

Chem. Ber. 93, 289-297 (1960) (https://www.thevespiary.org/rhodium/Rhodium/pdf/25-meo-phenethylchloride.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/25-meo-phenethylchloride.pdf)

The Preparation of Alkyl Chlorides
James F. Norris, Hazel B. Taylor

J. Am. Chem. Soc. 46(3), 753-757 (1924) (https://www.thevespiary.org/rhodium/Rhodium/pdf/alcohols2halides.hcl-zncl2.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/alcohols2halides.hcl-zncl2.pdf)

Phenylalkylamines with potential psychotherapeutic utility.  2.  Nuclear substituted 2-amino-1-phenylbutanes.
Standridge, Robert T.; Howell, Henry G.; Tilson, Hugh A.; Chamberlain, John H.; Holava, Henry M.; Gylys, Jonas A.; Partyka, Richard A.; Shulgin, Alexander T. 

Journal of Medicinal Chemistry  (1980),  23(2),  154-62. (https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin.2-amino-1-phenylbutanes.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin.2-amino-1-phenylbutanes.pdf)

Synthesis and body distribution of several iodine-131-labeled central nervous system active drugs.
Braun, Ulrich; Shulgin, Alexander T.; Braun, Gisela; Sargent, Thornton, III.

Journal of Medicinal Chemistry  (1977),  20(12),  1543-6. (https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin.iodinated.peas.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin.iodinated.peas.pdf)

1-[4-(3-Phenylalkyl)phenyl]-2-aminopropanes as 5-HT2A Partial Agonists
Cynthia S. Dowd, Katharine Herrick-Davis, Christina Egan, Ann DuPre, Carol Smith, Milt Teitler, and Richard A. Glennon

J. Med. Chem. 43(16) pp 3074 - 3084 (2000) (https://www.thevespiary.org/rhodium/Rhodium/pdf/glennon.partial.agonists.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/glennon.partial.agonists.pdf)
DOI:

10.1021/jm9906062 (http://dx.doi.org/10.1021/jm9906062)



Iodine-125 labeled 1-(2,5-dimethoxy-4-iodophenyl)-2-aminopropane: an iodinated radioligand that specifically labels the agonist high-affinity state of 5-HT2 serotonin receptors
Richard A. Glennon, Mark R. Seggel, William H. Soine, Katherine Herrick-Davis, Robert A. Lyon, Milt Titeler

J. Med. Chem. 31(1), 5-7 (1988) (https://www.thevespiary.org/rhodium/Rhodium/pdf/glennon.doi-125.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/glennon.doi-125.pdf)

Phenylalkylamines with potential psychotherapeutic utility. 1. 2-Amino-1-(2,5-dimethoxy-4-methylphenyl)butane
Robert T. Standridge, Henry G. Howell, Jonas A. Gylys, Richard A. Partyka, Alexander T. Shulgin

J. Med. Chem. 19(12), 1400-1404 (1976) (https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.4c-dom.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.4c-dom.pdf)

Phenylalkylamines with potential psychotherapeutic utility. 2. Nuclear substituted 2-amino-1-phenylbutanes
Robert T. Standridge, Henry G. Howell, Hugh A. Tilson, John H. Chamberlain, Henry M. Holava, Jonas A. Gylys, Richard A. Partyka, Alexander T. Shulgin

J. Med. Chem. 23(2), 154-162 (1980) (https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.nuclear.substituted.2-amino-1-phenylbutanes.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.nuclear.substituted.2-amino-1-phenylbutanes.pdf)

Potential psychotomimetics.  New bromoalkoxyamphetamines
Sepulveda, Silvia; Valenzuela, Ricardo; Cassels, Bruce K.

Journal of Medicinal Chemistry 15(4), 413-15 (1972) (https://www.thevespiary.org/rhodium/Rhodium/pdf/bromoalkoxyamphetamines.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/bromoalkoxyamphetamines.pdf)

Cross-linking and sequence-specific alkylation of DNA by aziridinylquinones. 3. Effects of alkyl substituents.
Hargreaves, Robert H. J.; O'Hare, C. Caroline; Hartley, John A.; Ross, David; Butler, John.   

Journal of Medicinal Chemistry  (1999),  42(12),  2245-2250. (https://www.thevespiary.org/rhodium/Rhodium/pdf/4-me-25-meo-propenylbenzene.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/4-me-25-meo-propenylbenzene.pdf)

Isomeric cyclopropyl ring-methylated homologs of trans-2-(2,5-dimethoxy-4-methylphenyl)cyclopropylamine, an hallucinogen analog.
Jacob, James N.; Nichols, David E.   

Journal of Medicinal Chemistry  (1982),  25(5),  526-30. (https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-methylated-cyclopropyl-peas.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-methylated-cyclopropyl-peas.pdf)

The article below is very interesting, as it contains novel routes to phenyl-2-propanones and other fun stuff.

2,4-Diaminothieno[2,3-d]pyrimidine analogs of trimetrexate and piritrexim as potential inhibitors of Pneumocystis carinii and Toxoplasma gondii dihydrofolate reductase.
Rosowsky, Andre; Mota, Clara E.; Wright, Joel E.; Freisheim, James H.; Heusner, James J.; McCormack, John J.; Queener, Sherry F.

Journal of Medicinal Chemistry 36, 3103-12 (1993) (https://www.thevespiary.org/rhodium/Rhodium/pdf/methoxy-p2p.wittig.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/methoxy-p2p.wittig.pdf)

For Tdurden969:
Electrosynthesis attempts of tetrahydridoborates
E. L. Gyenge & C. W. Oloman

Journal of Applied Electrochemistry 28(10), 1147-1151 (1998) (https://www.thevespiary.org/rhodium/Rhodium/pdf/borohydride.electrosynth.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/borohydride.electrosynth.pdf)

A new approach to electrochemical production of benzaldehyde from toluene in an undivided cell in the presence of the couple V5+/V4+
Qingfeng Y.,  Xiaoping L., Xiuling Z.

Journal of Applied Electrochemistry 33(3/4), 273-277 (2003) (https://www.thevespiary.org/rhodium/Rhodium/pdf/toluene2ba.vanadium.electro-ox.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/toluene2ba.vanadium.electro-ox.pdf)

A study on wastewater minimization in indirect electrochemical synthesis of benzaldehyde
Ding Zhoua, Zhirong Suna and Wanli Hu

Water Science and Technology 34(10), 113-120 (1996) (https://www.thevespiary.org/rhodium/Rhodium/pdf/toluene2ba.manganese.electro-ox.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/toluene2ba.manganese.electro-ox.pdf)
DOI:

10.1016/S0273-1223(96)00704-4 (http://dx.doi.org/10.1016/S0273%2D1223%2896%2900704%2D4)



For fallen_angel:
Friedel-Crafts and Related Reactions. Chapter 37, Section I-II: Alkene Acylation
C.D. Nenitzescu & A.T. Balaban

Volume III, Part 2, pp. 1032-1066 (https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1032-66.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1032-66.djvu)

Friedel-Crafts and Related Reactions. Chapter 37: References
C.D. Nenitzescu & A.T. Balaban

Volume III, Part 2, pp. 1136-1152 (https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1136-52.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1136-52.djvu)

A Convenient Preparation of Tetrahydro-4H-pyran-2-one
G. R. Owen & C. B. Reese

None (https://www.thevespiary.org/rhodium/Rhodium/pdf/beta-dichloroketones.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/beta-dichloroketones.pdf)

For Java:
Chemistry of nitrogen radicals. VI. The free-radical addition of dialkyl-N-chloramines to substituted olefins

J. Org. Chem.; 1967; 32(11); 3273-3284. (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/vinylic.aminochlorination.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/vinylic.aminochlorination.pdf)

Nonaromatic aminium radicals

Chem. Rev.; 1978; 78(3); 243-274. (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/nonaromatic.aminium.radicals.review.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/nonaromatic.aminium.radicals.review.pdf)

Radical addition of protonated N-chloroamines to olefins

Tet. Lett. 3163-3166 (1966) (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/radical.n-chloroamine.addn.alkenes.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/radical.n-chloroamine.addn.alkenes.pdf)

Synthesis of Arylpropylamines. I. From Allyl Chloride
T. M. Patrick, Jr., E. T. McBee, H. B. Hass;

J. Am. Chem. Soc.; 1946; 68(6); 1009-1011. (https://www.thevespiary.org/rhodium/Rhodium/pdf/amination.phenyl-2-chloropropane.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/amination.phenyl-2-chloropropane.pdf)

Synthesis of allylic amines through the palladium-catalyzed hydroamination of allenes

Tetrahedron Letters 36(22), 3857-3860 (1995) (https://www.thevespiary.org/rhodium/Rhodium/pdf/hydroamination.allenes.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/hydroamination.allenes.pdf)
DOI:

10.1016/0040-4039(95)00656-W (http://dx.doi.org/10.1016/0040%2D4039%2895%2900656%2DW)



Preparation of Aldehydes from Alkenes by the Addition of Carbon Monoxide and Hydrogen with Cobalt Carbonyls as Intermediates
Homer Adkins, George Krsek

J. Am. Chem. Soc. 70, 383-386 (1948) (https://www.thevespiary.org/rhodium/Rhodium/pdf/styrene.carbonylation.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/styrene.carbonylation.pdf)

Über die Beziehungen zwischen dem assym. Methyl-phenyl-äthylen-glycol und den ihm entsprechenden Anhydro-Formen
S. Danilow & E. Venus-Danilowa

Chem. Ber. 60, 1050-1069 (1927) (https://www.thevespiary.org/rhodium/Rhodium/djvu/hydratropaldehyde.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/hydratropaldehyde.djvu)

Chem. Ber. 89, 2641-2644 (1956) (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/cumylhydroperoxide.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/cumylhydroperoxide.pdf)

Arylation of several carbanions by the SRN1 mechanism
Roberto A. Rossi, J. F. Bunnett;

J. Org. Chem.; 1973; 38(17); 3020-3025. (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-1.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-1.pdf)

SRN1 phenylation of nitrile carbanions and ensuing reactions. New route to alkylbenzenes
J. F. Bunnett, Bernhard F. Gloor;

J. Org. Chem.; 1973; 38(24); 4156-4163. (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-2.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-2.pdf)

Mesitylation and phenylation of picolyl anions by the SRN1 mechanism
J. F. Bunnett, Bernhard F. Gloor;

J. Org. Chem.; 1974; 39(3); 382-384. (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-3.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-3.pdf)

Arylation of several carbanions by the SRN1 mechanism
Roberto A. Rossi and J. F. Bunnett

Journal of Organic Chemistry ,38,(17),pp 3020-3025 (1973) (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-4.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-4.pdf)

SRN1 phenylation of nitrile carbanions and ensuing reactions.  New route to alkylbenzenes
J. F. Bunnett and Bernhard F. Gloor

Journal of Organic chemistry, 38(24),pp 4156-4163 (1973) (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-5.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-5.pdf)

Mesitylation and phenylation of picolyl anions by the SRN1 mechanism
J. F. Bunnett and Bernhard F. Gloor

Journal of Organic chemistry, 39(3), pp 382-384 (1974) (https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-6.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-6.pdf)

Palladium-catalyzed arylation of siloxycyclopropanes with aryl triflates. Carbon chain elongation via catalytic carbon-carbon bond cleavage
Satoshi Aoki, Tsutomu Fujimura, Eiichi Nakamura, Isao Kuwajima

J. Am. Chem. Soc. 110, 3296-3298 (1988) (https://www.thevespiary.org/rhodium/Rhodium/pdf/arylation.pd-triflate.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/arylation.pd-triflate.pdf)
 
Ferrous ion catalysis of reactions of nucleophiles with aryl halides
Carlo Galli, J. F. Bunnett

J. Org. Chem. 49, 3041-3042 (1984) (https://www.thevespiary.org/rhodium/Rhodium/pdf/arylation.ferrous-srn1.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/arylation.ferrous-srn1.pdf)

For anyone intrerested in the above arylations, I suggest that you take a look at the articles below:

https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/alpha-arylation.html (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/alpha-arylation.html)


https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/alpha-arylation.carbonyls-nitriles.html (https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/alpha-arylation.carbonyls-nitriles.html)





Retrieved by ChemisTris:

For Rhodium:
Behavioral properties of psychoactive phenylisopropylamines in rats

European Journal of Pharmacology 76(4), 353-360 (1981) (http://mishmashblue.tripod.com/euro.pdf)

(http://mishmashblue.tripod.com/euro.pdf)

Synthesis of MDP2P

Synthetic Communications 24(2), 145 (1994) (http://mishmashblue.tripod.com/syncom.pdf)

(http://mishmashblue.tripod.com/syncom.pdf)

For Vitus_Verdegast:

Heterocycles 46, 91-94 (1997) (http://mishmashblue.tripod.com/heterocycles.djvu)

(http://mishmashblue.tripod.com/heterocycles.djvu)

J. Nat. Prod. 60(11), 1196-98 (1997) (http://mishmashblue.tripod.com/np60.pdf)

(http://mishmashblue.tripod.com/np60.pdf)

The Pharmacology and Clinical Pharmacology of 3,4-Methylenedioxymethamphetamine (MDMA, "Ecstasy")
A. Richard Green, Annis O. Mechan, J. Martin Elliott, Esther O'shea, M. Isabel Colado

Pharmacol. Rev., 5533-5600 (2003) (https://www.thevespiary.org/rhodium/Rhodium/pdf/mdma.pharmacology.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/mdma.pharmacology.pdf)
DOI:

10.1124/pr.55.3.3 (http://dx.doi.org/10.1124/pr.55.3.3)



Differences in potency and efficacy of a series of phenylisopropylamine/phenylethylamine pairs at 5-HT2A and 5-HT2C receptors
Claudio Acuña-Castillo, Claudio Villalobos, Pablo R. Moya, Patricio Sáez, Bruce K. Cassels, and J. Pablo Huidobro-Toro

None (https://www.thevespiary.org/rhodium/Rhodium/pdf/pea.receptor.potency-effiacy.differences.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/pea.receptor.potency-effiacy.differences.pdf)

For pHarmacist:

Tetrahedron Letters 10(39), 3375-3376 (1969) (http://mishmashblue.tripod.com/isotryptamine.pdf)

(http://mishmashblue.tripod.com/isotryptamine.pdf)



Retrieved by FreakyDMT:

For Rhodium:
10% Pd/C and HCOOH transfer hydrogenolysis of common protection groups

Indian journal of chemistry. Section B, 41(5):1064-1067 (2002) (https://www.thevespiary.org/rhodium/Rhodium/pdf/cth.protecting.group.removal.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/cth.protecting.group.removal.pdf)



Retrieved by Kinetic:

For Chimimanie:

Selective deprotection of esters using magnesium and methanol

Tet. Lett. 35(34), 6207-6210 (1994) (https://www.thevespiary.org/rhodium/Rhodium/pdf/ester.deprotection.mg-meoh.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/ester.deprotection.mg-meoh.pdf)
DOI:

10.1016/S0040-4039(00)73392-2 (http://dx.doi.org/10.1016/S0040%2D4039%2800%2973392%2D2)





Retrieved by Lego:

For Rhodium:
J Chem Res (Miniprint) 1137-1145 (1982)

http://www.angelfire.com/scifi2/lego/journals/7.pdf (http://www.angelfire.com/scifi2/lego/journals/7.pdf)


http://www.angelfire.com/scifi2/lego/journals/8.pdf (http://www.angelfire.com/scifi2/lego/journals/8.pdf)



For Chimimanie:
Phenylbutanoids from Zingiber cassumunar.    
Tuntiwachwuttikul, Pittaya; Pancharoen, Orasa; Jaipetch, Thaworn; Reutrakul, Vichai.   

Phytochemistry (Elsevier)  (1981),  20(5),  1164-5. (http://lego.chemistry.tripod.com/Journals/1164.djvu)

(http://lego.chemistry.tripod.com/Journals/1164.djvu)

Studies on Thai medicinal plants.  Part VIII.  Further characterization of the constituents of a Thai medicinal plant, Zingiber cassumunar Roxb.  
Kuroyanagi, Masanori; Fukushima, Seigo; Yoshihira, Kunitoshi; Natori, Shinsaku; Dechatiwongse, Thaweephol; Mihashi, Kunihide; Nishi, Masatoshi; Hara, Shuuji.    

Chemical & Pharmaceutical Bulletin  (1980),  28(10),  2948-59 (http://lego.chemistry.tripod.com/Journals/2948.djvu)

(http://lego.chemistry.tripod.com/Journals/2948.djvu)

Synthesis and hypolipidemic activity of modified side chain a-asarone homologues    
Cruz, Adriana; Garduno, Leticia; Salazar, Maria; Martinez, Elizdath; Jimenez-Vazquez, Hugo A.; Diaz, Francisco; Chamorro, German; Tamariz, Joaquin.

Arzneimittel-Forschung  (2001),  51(7),  535-544 (http://lego.chemistry.tripod.com/Journals/535.djvu)

(http://lego.chemistry.tripod.com/Journals/535.djvu)

For Vitus-Verdegast:

J. Pharm. Sci., 1967, 56, 970-973 (http://lego.chemistry.tripod.com/Journals/TF-Amph.djvu)

(http://lego.chemistry.tripod.com/Journals/TF-Amph.djvu) later addition (02-15-04):
Trifluromethyl analogs of amphetamine and norephedrine
Roger M. Pinder, Alfred Burger

Arzneimittel-Forschung , 1970, 20, 245-246 (http://lego.chemistry.tripod.com/Journals/CN-Amph.djvu)

(http://lego.chemistry.tripod.com/Journals/CN-Amph.djvu) later addition (02-15-04):
m- and p-Hydroxy-1-cyanophenethylamine
Roger M. Pinder, Alfred Burger, E. J. Ariens

For Azole
Synthesis of Concave Receptors Derived from Diphenylglycoluril. later addition (02-15-04):
Sijbesma, R. P.; Nolte, R. J. M.

Recl. Trav. Chim. Pays-Bas, 1993, 112, 643-647 (http://lego.chemistry.tripod.com/Journals/quinone-PTC.djvu)

(http://lego.chemistry.tripod.com/Journals/quinone-PTC.djvu)
Synthesis of 1,4-bis(2-chloroethoxy)benzene by PTC alkylation of hydroquinone (ref. #23 from

Dihydrobenzofuran Analogues of Hallucinogens. 3.  (https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-dihydrobenzofuran-3-fly.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-dihydrobenzofuran-3-fly.pdf)):





Retrieved by moo:

For Chimimanie:
Synthesis of compounds with potential central nervous system stimulant activity. I.
2-Amino-2-oxazolin-4-one-5-spirocycloalkanes and 2-amino-2-oxazolin-4-one-5-spiro(4'-piperidines)

Michael R. Harnden, Ray R. Rasmussen

J. Med. Chem. 12, 919-921 (1969) (https://www.thevespiary.org/rhodium/Rhodium/pdf/spiro-oxazolines-1.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/spiro-oxazolines-1.pdf)

Synthesis of compounds with potential central nervous system stimulant activity. II.
5-Spiro-substituted 2-amino-2-oxazolines

Michael R. Harnden, Ray R. Rasmussen

J. Med. Chem. 13, 305-308 (1970) (https://www.thevespiary.org/rhodium/Rhodium/pdf/spiro-oxazolines-2.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/spiro-oxazolines-2.pdf)

Synthesis and serotonin receptor affinities of a series of enantiomers of a-methyltryptamines:  evidence for the binding conformation of tryptamines at serotonin 5-HT1B receptors.
Nichols, David E.; Lloyd, David H.; Johnson, Michael P.; Hoffman, Andrew J.   

Journal of Medicinal Chemistry  (1988),  31(7),  1406-12. (https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-amt-enantiomers.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-amt-enantiomers.pdf)




Retrieved by Java:

For Rhodium:
4-bromo-2,5-dimethoxyphenethylamine (2C-B): A review of the public domain literature.
Cole M.D,Lea C and Oxley N.

Science & Justice 42(4), 223-224 (2002) (https://www.thevespiary.org/rhodium/Rhodium/pdf/2c-b.review.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/2c-b.review.pdf)

For ChemisTris:

New synthetic route for the preparation of potentially hypocholesterolemic analogs of alpha-asarone.
Determination of E/Z isomer content in natural and synthetic mixtures of alpha-asarone and its analogs.

Munoz, Heber; Diaz, Francisco; Sanchez, Adrian; Barajas, Marcelino; Labarrios, Fernando; Tamariz, Joaquin.   

Acta Mexicana de Ciencia y Tecnologia, 11(41), 51-62 (1993) (https://www.thevespiary.org/rhodium/Rhodium/pdf/asarone.nueva.ruta.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/asarone.nueva.ruta.pdf)



Retrieved by 7is:

For Manichi:
Binding of Phenylalkylamine Derivatives at 5-HT1C and 5-HT2 Serotonin Receptors: Evidence for a Lack of Selectivity
Richard. A. Glennon

J. Med. Chem, 734 (1992) (http://nic-nac-project.de/~tajkor/jm00082a014.pdf)

(http://nic-nac-project.de/~tajkor/jm00082a014.pdf)

The Ethyl Homologs of 2,4,5-Trimethoxyphenylisopropylamines
Alexander T. Shulgin

J. Med. CHem 11, 196-187 (1968) (http://nic-nac-project.de/~tajkor/jm00307a056.pdf)

(http://nic-nac-project.de/~tajkor/jm00307a056.pdf)

For Rhodium:
Drug Discrimination and Receptor Binding Studies of N-Isopropyl Lysergamide Derivates
Huang, Marona-Lewicka, Pfaff, Nichols

Pharmacology, Biochmistry and Behavior 47(3), 667-673 (1994) (https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-n-isopropyl-lysergamide.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-n-isopropyl-lysergamide.pdf)

Ergot Peptide Alkaloid Spectra of Claviceps-Infected Tall Fescue, Wheat, and Barley
James K. Porter, Charles W. Bacon, Ronald D. Plattner, and Richard F. Arrendale.

J. Agric. Food Chem. 35, 359-361 (1987) (https://www.thevespiary.org/rhodium/Rhodium/pdf/ergot.peptide.alkaloid.spectra.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/ergot.peptide.alkaloid.spectra.pdf)

Synthesis of some fluorinated nitro-olefins
R. Jacobo, A. Cota, E. Rogel, J. D. Garcia, I. A. Rivero, L. H. Hellberg and R. Somanathan

Journal of Fluorine Chemistry, 67(3), 253-255 (1994) (http://nic-nac-project.de/~tajkor/17.pdf)

(http://nic-nac-project.de/~tajkor/17.pdf)
DOI:

10.1016/0022-1139(93)02969-L (http://dx.doi.org/10.1016/0022%2D1139%2893%2902969%2DL)



For Potter
Colour reactions of some aromatic ethers found in essential oils
Janet E. Forrest, R. Richard and R. A. Heacock

Journal of Chromatography A, 65(2), 439-444 (1972) (http://nic-nac-project.de/~tajkor/18.pdf)

(http://nic-nac-project.de/~tajkor/18.pdf)

For Vitus
1-Ethynylphenethylamine
Alfred Burger, Stuart E. Zimmerman, and E. J. Ariëns

J. Med. Chem. 9, 469 (1966) (http://nic-nac-project.de/~tajkor/19.pdf)

(http://nic-nac-project.de/~tajkor/19.pdf)

For Ganesha:
Forty years of hydride reductions latest addition (03-19-04):
Herbert C. Brown and S. Krishnamurthy
Tetrahedron 1979, 35, 567-607 (1979)

(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_imgs/pdf.gif)





Retrieved by dioulasso:

For Rhodium:
Copper(II)-B-cyclodextrin aided oxidation of eugenol

Indian Journal Of Chemistry. Sect. B. 42(2), 369-371 (2003) (https://www.thevespiary.org/rhodium/Rhodium/djvu/cu-cyclodextrin.eugenol.ox.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/cu-cyclodextrin.eugenol.ox.djvu)

Zinc/hydrazine: A low cost-facile system for the reduction of nitro compounds

Indian Journal Of Chemistry. Sect. B.  42(1), 180-183 (2003) (https://www.thevespiary.org/rhodium/Rhodium/djvu/nitro2amine.zn-n2h4.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/nitro2amine.zn-n2h4.djvu)

Reduction of oximes with NaBH4/CuSO4/MeOH

Indian journal of chemistry. Section B,  41(5):1072-1074 (2002) (https://www.thevespiary.org/rhodium/Rhodium/djvu/oxime-reduction.nabh4-cuso4.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/oxime-reduction.nabh4-cuso4.djvu)

NaBH4/I2 reductive amination

Indian Journal of Chemistry Sect. B, 41(9), 1970-1971 (2002) (https://www.thevespiary.org/rhodium/Rhodium/djvu/redamin.nabh4-i2.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/redamin.nabh4-i2.djvu)
(claimed to work only for benzaldehydes, not aliphatic carbonyl compounds)

For Vitus Verdegast:
Solvent-free Microwave Knoevenagel condensation catalyzed by NaCl or NH4OAc-AcOH

Indian Journal of Chemistry, Sect. B. 39(6), 403-405 (2000) (https://www.thevespiary.org/rhodium/Rhodium/djvu/knoevenagel.zncl2.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/knoevenagel.zncl2.djvu)

Cobalt(II)Chloride Hexahydrate - Zinc - DMF - Water: An Efficient System for the Reduction of Aldehydes to Alcohols

Indian Journal of Chemistry, Sect. B. 33, 182-183 (1994) (https://www.thevespiary.org/rhodium/Rhodium/djvu/aldehyde2alcohol.cocl2-zn-dmf-h2o.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/aldehyde2alcohol.cocl2-zn-dmf-h2o.djvu)



Retrieved by Azole:

For fallen_Angel:
2,4,5-trimethoxybenzaldehyde from vanillin

None (http://hyperlab.0catch.com/J_Chem_Soc_C_2222.djvu)

(http://hyperlab.0catch.com/J_Chem_Soc_C_2222.djvu)

pyrylium salts by Ac2O/HClO4 diacylation of olefins

None (http://hyperlab.0catch.com/TL1968_4643.djvu)

(http://hyperlab.0catch.com/TL1968_4643.djvu)

For Rhodium:

A Convenient Preparation of Conjugated Nitro Olefins by Electrochemical Method.
A. Kunai, Y. Yanagi, and K. Sasaki

None (http://hyperlab.0catch.com/TL_1983_v24_No41_4443.djvu)

(http://hyperlab.0catch.com/TL_1983_v24_No41_4443.djvu)

Studies on the Formation of Complex Oxidation and Condensation Products of Phenols. A Contribution to the Investigation of the Origin and Nature of Humic Acid. Part I. - Studies of the Reactivity of Simple Monocyclic Quinones. later addition (03-09-04):
H. G. H. Erdtman

None (http://hyperlab.0catch.com/Erdtman_I.djvu)

(http://hyperlab.0catch.com/Erdtman_I.djvu)

Studies on the Formation of Complex Oxidation and Condensation Products of Phenols. Part II.
Coupling of Simple Phenols and Quinones to Diphenyl Derivatives.
later addition (03-09-04):
H. G. H. Erdtman

None (http://hyperlab.0catch.com/Erdtman_II.djvu)

(http://hyperlab.0catch.com/Erdtman_II.djvu)


For pHarmacist:
A One-step Ester to Hydrocarbon Reduction.
Donald C. Wigfield and Kevser Taymaz

None (http://hyperlab.0catch.com/TL_1973_49_4841.djvu)

(http://hyperlab.0catch.com/TL_1973_49_4841.djvu)

Diels-Alder route to precursors of anthranilic acid derivatives
K. Gewald,

None (https://www.thevespiary.org/rhodium/Rhodium/djvu/chem.ber.99.1002.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/chem.ber.99.1002.djvu)

For Chimimanie:
Indoles.  XXXII.  Synthesis of tryptophols.
Grandberg, I. I.; Moskvina, T. P.

None (http://hyperlab.0catch.com/KhGS_1972_1366.djvu)

(http://hyperlab.0catch.com/KhGS_1972_1366.djvu)
This article is reviewed in the book "Preparative Chemistry of Indole" (in Russian) along with several other articles concerning tryptophols by the same author (I.I.Grandberg).

Darstellung und Reduktion von Indolyl-(3)-aminomethylketonen
K.Bodendorf, A.Walk

Arch. Pharm.  (1961),  294  484-7 (https://www.thevespiary.org/rhodium/Rhodium/djvu/bodendorf.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/bodendorf.djvu)

None (http://hyperlab.0catch.com/Derivati_Indolici_IV.djvu)

(http://hyperlab.0catch.com/Derivati_Indolici_IV.djvu)

None (http://hyperlab.0catch.com/Derivati_Indolici_VI.djvu)

(http://hyperlab.0catch.com/Derivati_Indolici_VI.djvu)

None (http://hyperlab.0catch.com/Derivati_Indolici_VII.djvu)

(http://hyperlab.0catch.com/Derivati_Indolici_VII.djvu)


For GC_MS:
A new synthesis of methoxalen.
P Nore, E Honkanen

None (http://hyperlab.0catch.com/JHetChem1980_17_985.djvu)

(http://hyperlab.0catch.com/JHetChem1980_17_985.djvu)

For Ruthenium:
The Reimer-Tiemann Reaction, Enhanced by Ultrasound later addition (03-15-04):
John C. Cochran and Margaret G. Melville
Synth. Commun., 1990, 20(4), 609-616.

(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_imgs/djvu.gif)



For Nicodem:
Ethyl nitroacetate from acetoacetic ester later addition (03-15-04):
V. M. Rodionov, E. V. Machinskaya, and V. M. Belikov
Zh. Obshch. Khim., 18, 917-920 (1948) (in Russian).

(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_imgs/djvu.gif)



For Lego:
An efficient method for the conversion of phenolic Mannich bases to C-methylated phenols. Synthesis of 3,6-dimethylcatechol. later addition (02-15-04):
Sinhababu, A. K.; Borchardt, R. T.

None (http://hyperlab.0catch.com/SynthCommun1982_12_983.djvu)

(http://hyperlab.0catch.com/SynthCommun1982_12_983.djvu)

Selective ring C-methylation of hydroxybenzaldehydes via their Mannich bases. later addition (02-15-04):
Sinhababu, A. K.; Borchardt, R. T.

None (http://hyperlab.0catch.com/SynthCommun1983_13_677.djvu)

(http://hyperlab.0catch.com/SynthCommun1983_13_677.djvu)

Alkene Reductions Employing Ethyl Acetate - Hydroxylamine, a Useful New Source of Diimide
P. A. Wade, N. V. Amin

None (http://hyperlab.0catch.com/SynthCommun1982_12_287_1.djvu)

(http://hyperlab.0catch.com/SynthCommun1982_12_287_1.djvu)

An improved preparation of phenylacetone.
J. Kizlink

None (http://hyperlab.0catch.com/ChemickeListy_1990_84_993.djvu)

(http://hyperlab.0catch.com/ChemickeListy_1990_84_993.djvu) 

Oxidation of nitromethane by manganese(III) acetate:  novel formation of methyl radical.
Srivastava, Ranjan P.; Seth, M.; Bhaduri, A. P.

None (http://hyperlab.0catch.com/IndJChem_1989_28B_65.djvu)

(http://hyperlab.0catch.com/IndJChem_1989_28B_65.djvu)

Synthesis of nitroalkanes from bromoalkanes by phase-transfer catalysis.
Sane, Pramodchandra V.; Sharma, Man Mohan

None (http://hyperlab.0catch.com/OPPI_1988_20_598.djvu)

(http://hyperlab.0catch.com/OPPI_1988_20_598.djvu)

Preparation of N-unsubstituted thioamides by a modified Willgerodt-Kindler reaction.
You, Qidong; Zhou, Houyuan; Wang, Qizhou; Lei, Xinghan

None (http://hyperlab.0catch.com/OPPI_1991_23_435.djvu)

(http://hyperlab.0catch.com/OPPI_1991_23_435.djvu)

Improved synthesis of phenylacetamides by the Willgerodt reaction with microwave heating.
Strauss, Christopher R.; Trainor, Robert W.

None (http://hyperlab.0catch.com/OPPI_1995_27_552.djvu)

(http://hyperlab.0catch.com/OPPI_1995_27_552.djvu)

Selective reduction of nitro compounds with titanium(II) reagents.
J. George and S. Chandrasekaran

None (http://hyperlab.0catch.com/SynthCommun_1983_13_495.djvu)

(http://hyperlab.0catch.com/SynthCommun_1983_13_495.djvu)

The following articles are in Russian:

Methylation of phenol with methyl formate.
Nasadyuk, V. A.; Fedevich, E. V.; Pazderskii, Yu. A.; Moiseev, I. I.   

None (http://hyperlab.0catch.com/IzvAN_1989_787.djvu)

(http://hyperlab.0catch.com/IzvAN_1989_787.djvu)

Reactions of hydrazine derivatives. XVII. New synthesis of ?-methyltryptophol.
Grandberg, I. I.; Kost, A. N.; Terent'ev, A. P.

None (http://hyperlab.0catch.com/ZhOKh_1957_3342.djvu)

(http://hyperlab.0catch.com/ZhOKh_1957_3342.djvu)

Abstract
Heating 10.8 g. PhNHNH2, 10.2 g. AcCH2CH2CH2OH, and 6 ml. AcOH 0.5 hr. at 100° gave after addn. of NH4OH and extn. with Et2O 88.5% PhNHN:CMeCH2CH2CH2OH (I), b8 194-6°, m. 60-6°.  Reaction of 51 g. AcCH2CH2CH2Cl and 48.6 g. PhNHNH2 in EtOH gave after 1 hr. on steam bath 52.4% 1-phenyl-3-methyl-1,4,5,6-tetrahydropyridazine, b6 197-8° (picrate, m. 226.5°).  Heating 15.7 g. PhNHNH2 and 15.3 g. AcCH2CH2CH2OH 1 hr. on steam bath, heating in vacuo to 150° to remove H2O, addn. of 0.2 g. Cu2Cl2 and heating to 230° 2 hrs. gave 69.4% a-methyltryptophol (II), b7-8 202-4°, m. 52-5° (picrate, m. 132°); use of ZnCl2 as catalyst gave 63% yield.  I and AcCl in dioxane-CCl4 gave 33.4% O-acetyl-a-methyltryptophol, b3-4 196-204° (picrate, m. 131.5°), also formed from II and Ac2O at reflux.  II and PBr3 in Et2O gave after an aq. treatment 70.3% a-methyl-b-(b-bromoethyl)indole, m. 58°, which with aq. Me2NH at 100° gave 66.5% a-methyl-b-(b-dimethylaminoethyl)indole, b21 204-5°, m. 93-5° (picrate, m. 176°).  Cf. Hoshinyo, et al. C.A. 29, 79757.

For 1kplateau:
Supramolecular catalytic systems based on cyclodextrins in Wacker oxidation. later addition (03-09-04):
E. A. Karakhanov, A. Ya. Zhuchkova, T. Yu. Filippova, A. L. Maximov

None (http://hyperlab.0catch.com/Neftekhimia2003_43_302.djvu)

(http://hyperlab.0catch.com/Neftekhimia2003_43_302.djvu)

   The article is written in Russian. There exists an English version of the journal (the page number you cited probably refers to the translation) but I've never seen it. Most of the references are in English. The yields are not very encouraging, and the modified cyclodextrins applied are not commercially available. Anyway, I'll try to translate the article if you like.

Wacker oxidation of various 1-alkenes (1-hexene to 1-dodecene) and p-substituted styrenes was performed under 5 MPa pressure of O2 in a biphasic system water - alkene in the presence of palladium sulfate and modified beta-cyclodextrins (see Fig. 1). Copper salts were applied as a co-catalyst. Oxidation of 1-alkenes led to the corresponding methyl ketones; styrenes gave mixtures of acetophenones and arylacetaldehydes.



Retrieved by Zamboni:

For Chimimanie:
a-Asarone congeners as hypolipidemic agents. Pseudoreceptor versus minireceptor modeling. later addition (03-09-04):   
Filipek, Slawomir; Lozowicka, Bozena.    Department of Chemistry,  Warsaw University,  Warsaw,  Pol.   

Acta Poloniae Pharmaceutica  (2000),  57(Suppl.),  106-109.  (https://www.thevespiary.org/rhodium/Rhodium/djvu/Acta2000.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/Acta2000.djvu)

Indigo to alpha-Methyltryptamine later addition (03-09-04):
S. Pietra and G. Tacconi

None (https://www.thevespiary.org/rhodium/Rhodium/djvu/Farmaco58-893-910b.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/Farmaco58-893-910b.djvu)
(If anyone wants to see the 1957 Farmaco article that's listed as a reference in the 1958 Farmaco article, I have that, too. Of course there is a US patent which describes the process:

Patent US3282959 (http://l2.espacenet.com/dips/viewer?PN=US3282959&CY=gb&LG=en&DB=EPD)

)


For Rhodium:
The part that I copied before my money ran out for the xerox machine:
5-Hydroxyvanillin to Myristicinaldehyde in 77% Yield later addition (03-09-04):
Taniguchi, Eiji; Imamura, Keiichi; Ishabashi, Fumito; Matsui, Toshio; Nishio, Akira

Agric. Biol. Chem.; 53(3) 631-644 (1989) (https://www.thevespiary.org/rhodium/Rhodium/djvu/agrbiochem53-635-643.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/agrbiochem53-635-643.djvu)

Isomerization of some allylbenzenes in a microwave batch reactor later addition (03-09-04):
Le, Ngoc Thach; Strauss, Christopher R.

Tap Chi Hoa Hoc 38(1), 76-79 (2000) (https://www.thevespiary.org/rhodium/Rhodium/djvu/TapChi38-76-79.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/TapChi38-76-79.djvu)

For Kinetic:
Zinc chloride catalysed 2,2-dialkyl benzodioxole acylations with acetic anhydride, yields over 90% later addition (03-09-04):

Indian J.Chem.Sect.B; 38; 2; 1999; 137 - 140. (https://www.thevespiary.org/rhodium/Rhodium/djvu/indjchem38b-137-140.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/indjchem38b-137-140.djvu)



Retrieved by pHarmacist:

For Chimimanie:
Analogs of amphetamine. 6. 2,5-Dimethoxy-4-methyl- and 2,5-dimethoxy-alpha,4-dimethylphenylalanines
Beng T. Ho, L. Wayne Tansey, Jen-Tzaw Huang;

J. Med. Chem.; 1971; 14(11); 1132-1133 (http://pharmacist.the-hive.tripod.com/alal-amphet.pdf)

(http://pharmacist.the-hive.tripod.com/alal-amphet.pdf)

2,5-Dimethoxy-4-methylphenylalanine
Roger M. Pinder, Keith Brewster;

J. Med. Chem.; 1971; 14(7); 650-651 (http://pharmacist.the-hive.tripod.com/25dimeo4me.pdf)

(http://pharmacist.the-hive.tripod.com/25dimeo4me.pdf)

Dihydroxynitrobenzaldehydes and hydroxymethoxynitrobenzaldehydes: synthesis and biological activity as catechol-O-methyltransferase inhibitors
Rosa A. Perez, Eldiberto Fernandez-Alvarez, Ofelia Nieto, F. Javier Piedrafita;

J. Med. Chem.; 1992; 35(24); 4584-4588 (http://pharmacist.the-hive.tripod.com/benzald.pdf)

(http://pharmacist.the-hive.tripod.com/benzald.pdf)

Phenylalkylamines with potential psychotherapeutic utility. 1. 2-Amino-1-(2,5-dimethoxy-4-methylphenyl)butane
Robert T. Standridge, Henry G. Howell, Jonas A. Gylys, Richard A. Partyka, Alexander T. Shulgin;

J. Med. Chem.; 1976; 19(12); 1400-1404 (http://pharmacist.the-hive.tripod.com/Phenylalk.pdf)

(http://pharmacist.the-hive.tripod.com/Phenylalk.pdf)

beta-Chloroethylamines related to mescaline
Cooper, Paul D.

Journal of Medicinal Chemistry 16, 1057-9 (1973) (http://pharmacist.the-hive.tripod.com/meschalo.pdf)

(http://pharmacist.the-hive.tripod.com/meschalo.pdf)



Retrieved by Lugh:

For Lego:
New Sulfur Derivatives Of Indoles

Rocz. Chem.; 50; 1976; 603. (https://www.thevespiary.org/rhodium/Rhodium/djvu/piotrowska.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/piotrowska.djvu)
Lego's voice: N,N-substituted indol-3-yl-thioacetamides could bee valuable precursors for N,N-substituted tryptamines as thioamides are easily reduced to the corresponding amines.

For Potter:
Acetophenone to Phenylacetone: PhCOCH3 + CH2N2 --AlCl3--> P2P (50%)
Katalysierte Homologisierung Cycloaliphatischer und Aliphatischer Ketone mit Diazoalkanen
Eugen Müller, Martin Bauer

None (https://www.thevespiary.org/rhodium/Rhodium/pdf/diazomethane.ketone.homologation.pdf)

(https://www.thevespiary.org/rhodium/Rhodium/pdf/diazomethane.ketone.homologation.pdf)

For Barium:
The Darzen Condensation, Part I

J. Chem. Soc. C (1970), 1154 (https://www.thevespiary.org/rhodium/Rhodium/djvu/sipos1.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/sipos1.djvu)

The Darzen Condensation, Part III

J. Chem. Soc., Perkin Trans. 2 (1975), 805 (https://www.thevespiary.org/rhodium/Rhodium/djvu/sipos2.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/sipos2.djvu)

Stereochemical Control of the Darzens Condensation

J.Chem. Soc., Chem. Commun. (1977), 902 (https://www.thevespiary.org/rhodium/Rhodium/djvu/jonczyk.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/jonczyk.djvu)

Synthesis of Glycidic esters in a two-phase solid-liquid system

Synth. Commun. (1982), 12, 355 (https://www.thevespiary.org/rhodium/Rhodium/djvu/gladiali.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/gladiali.djvu)

For pHarmacist:
Indolylalkylamines From Arylhydrazines and gamma- and delta-Halocarbonyl Compounds (Review)
Grandberg, I. I.

Chem. Heterocycl. Compd. (engl. Transl.) 1974, 10, 501. (https://www.thevespiary.org/rhodium/Rhodium/djvu/grundberg.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/grundberg.djvu)

Structural Correlation between Apomorphine and LSD:
Involvement of Dopamine as well as Serotonin in the Actions of Hallucinogen

Dave E. Nichols

J. Theor. Biol. 59, 167-177 (1976) (https://www.thevespiary.org/rhodium/Rhodium/djvu/nichols.djvu)

(https://www.thevespiary.org/rhodium/Rhodium/djvu/nichols.djvu)

For Rhodium:
Sodium borohydride: A versatile reagent in the reductive N-monoalkylation of SMF 2.0.19 | SMF © 2021, Simple Machines