The thread
Post 217986
(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
(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
(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-dimethyltryptamineComptes Rendus des Seances de l'Academie des Sciences, Serie C: Sciences Chimiques (1969), 269(1), 51-3http://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/indole%20thio%20amide.PDF
For Kinetic:http://members.lycos.co.uk/chimimanie/chlorodifluoromethane.pdf
For Rhodium:2,5-Dimethoxyallylbenzene isomerization with PdCl2(MeCN)2Aust. J. Chem. 43, 777-781 (1990)http://members.lycos.co.uk/chimimanie/austjchem-777-1990.PDF
Synthesis of MethadoneBull. Soc. Chim. Belg. 90(9), 977-82 (1981)http://members.lycos.co.uk/chimimanie/BSCBelg977-1981.PDF
For Vitus_Verdegast:5-iodo-2-aminoindan, a non-neurotoxic analogue of p-iodo-amphetamineNichols, 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)
DOI:
10.1016/0091-3057(91)90601-W
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
Retrieved by Rhodium:For roger2003:Zur Kenntnis der GlyoxylsäureHans MeyerChem. Ber. 34, 3593-93 (1904)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/glyoxylic.ber.37.3592.1904.pdf)
For pHarmacist:Deveral Derivatives of p-Chlorophenoxyacetic AcidN. A. Zakharova, et al.Chemical Abstracts, Vol 63, 17948 (1965)
(
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 AgonistH. Schmidhammer, A. Schratz, J. MitterdorferHelv. Chim. Acta. 73, 1784-87 (1990)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/14-methoxymetopon.pdf)
For Lego:S-Oxidation products of alkylthioamphetaminesRezende, 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)
Bromodecarbonylation and Bromodecarboxylation of Electron-Rich Benzaldehydes and Benzoic Acids with Oxone® and Sodium BromideBon-Suk Koo; Eun-Hoo Kim; Kee-Jung LeeSynthetic Communications 32(15), 2275-2286 (2002)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/bromodecarbo_ylation.nabr-oxone.pdf)
DOI:
10.1081/SCC-120005997
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)
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 lactamsDennis BrillonSynthetic Communications 20(19), 3085-3095 (1990)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/amide-thionation.pdf)
Abstract: An agent, prepd. from 1:1 P
2S
5 and Na
2CO
3 in situ, is used for thionation of amides, amino acids, peptides, and lactams. Yields range from 28 to 96%.
As mentioned in:
Post 468717
(Lego: "Amide to thioamide to amine", Serious Chemistry)For Aurelius:Direct Conversions of Ethers to Esters by Trichloroisocyanuric AcidTet. Lett. 55, 5819-5820 (1968)
(
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)
Oxidation Studies of Symmetrical and Unsymmetriclal Ethers - Comparison of Trichloroisocyanuric Acid and Hypochlorous AcidTetrahedron 27, 2671-2674 (1971)
(
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 ClayJ. Chem. Soc. Perkin Trans 1, 3519-3520 (1994)
(
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)
For Vitus_Verdegast: Org. Proc. Res. Dev. 4, 534-543 (2000)
(
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)
For Captain_Mission:Direct conversion of Bromohydrins to ketones by a free radical elimination of HBrJ. Org. Chem. Vol. 67(1), 312-313(2002)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/bromohydrin2ketone.pdf)
Simple, inexpensive procedure for the large-scale production of alkyl quinonesJ. Org. Chem.; 1983; 48(17); 2932-2933.
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/large-scale.alkyl-quinones.pdf)
For Ganesha:Amphetamine Analogs. II. Methylated Phenethylamines
(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)
Psychotropic Phenylisopropylamines derived from Apiole and Dillapiole
(03-15-04):Alexander T. ShulginNature 215, 1494-95 (1967)
(
https://www.thevespiary.org/rhodium/Rhodium/chemistry/dmmda.shulgin.html)
Structure-Activity Relationships of One-Ring Psychotomimetics
(03-15-04):Alexander T. Shulgin, Thornton Sargent, Claudio NaranjoNature 221, 537-541 (1969)
(
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
Acta Pharm. Suecia 16, 267-270 (1979)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-dihydroisoquinolineLora-Tamayo, Manuel; Madronero, Ramon; Munoz, Guillermo GarciaChem. Ber. 93, 289-297 (1960)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/25-meo-phenethylchloride.pdf)
The Preparation of Alkyl ChloridesJames F. Norris, Hazel B. TaylorJ. Am. Chem. Soc. 46(3), 753-757 (1924)
(
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)
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)
1-[4-(3-Phenylalkyl)phenyl]-2-aminopropanes as 5-HT2A Partial AgonistsCynthia S. Dowd, Katharine Herrick-Davis, Christina Egan, Ann DuPre, Carol Smith, Milt Teitler, and Richard A. GlennonJ. Med. Chem. 43(16) pp 3074 - 3084 (2000)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/glennon.partial.agonists.pdf)
DOI:
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 receptorsRichard A. Glennon, Mark R. Seggel, William H. Soine, Katherine Herrick-Davis, Robert A. Lyon, Milt TitelerJ. Med. Chem. 31(1), 5-7 (1988)
(
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)butaneRobert T. Standridge, Henry G. Howell, Jonas A. Gylys, Richard A. Partyka, Alexander T. ShulginJ. Med. Chem. 19(12), 1400-1404 (1976)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.4c-dom.pdf)
Phenylalkylamines with potential psychotherapeutic utility. 2. Nuclear substituted 2-amino-1-phenylbutanesRobert T. Standridge, Henry G. Howell, Hugh A. Tilson, John H. Chamberlain, Henry M. Holava, Jonas A. Gylys, Richard A. Partyka, Alexander T. ShulginJ. Med. Chem. 23(2), 154-162 (1980)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/shulgin/shulgin.nuclear.substituted.2-amino-1-phenylbutanes.pdf)
Potential psychotomimetics. New bromoalkoxyamphetaminesSepulveda, Silvia; Valenzuela, Ricardo; Cassels, Bruce K.Journal of Medicinal Chemistry 15(4), 413-15 (1972)
(
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)
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)
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)
For Tdurden969:Electrosynthesis attempts of tetrahydridoboratesE. L. Gyenge & C. W. OlomanJournal of Applied Electrochemistry 28(10), 1147-1151 (1998)
(
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)
A study on wastewater minimization in indirect electrochemical synthesis of benzaldehydeDing Zhoua, Zhirong Suna and Wanli HuWater Science and Technology 34(10), 113-120 (1996)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/toluene2ba.manganese.electro-ox.pdf)
DOI:
10.1016/S0273-1223(96)00704-4
For fallen_angel:Friedel-Crafts and Related Reactions. Chapter 37, Section I-II: Alkene AcylationC.D. Nenitzescu & A.T. BalabanVolume III, Part 2, pp. 1032-1066
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1032-66.djvu)
Friedel-Crafts and Related Reactions. Chapter 37: ReferencesC.D. Nenitzescu & A.T. BalabanVolume III, Part 2, pp. 1136-1152
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/alkene.acylation.1136-52.djvu)
A Convenient Preparation of Tetrahydro-4H-pyran-2-oneG. R. Owen & C. B. ReeseNone
(
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 olefinsJ. Org. Chem.; 1967; 32(11); 3273-3284.
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/vinylic.aminochlorination.pdf)
Nonaromatic aminium radicalsChem. Rev.; 1978; 78(3); 243-274.
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/nonaromatic.aminium.radicals.review.pdf)
Radical addition of protonated N-chloroamines to olefinsTet. Lett. 3163-3166 (1966)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/archive/radical.n-chloroamine.addn.alkenes.pdf)
Synthesis of Arylpropylamines. I. From Allyl ChlorideT. 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)
Synthesis of allylic amines through the palladium-catalyzed hydroamination of allenesTetrahedron Letters 36(22), 3857-3860 (1995)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/hydroamination.allenes.pdf)
DOI:
10.1016/0040-4039(95)00656-W
Preparation of Aldehydes from Alkenes by the Addition of Carbon Monoxide and Hydrogen with Cobalt Carbonyls as IntermediatesHomer Adkins, George KrsekJ. Am. Chem. Soc. 70, 383-386 (1948)
(
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-FormenS. Danilow & E. Venus-DanilowaChem. Ber. 60, 1050-1069 (1927)
(
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)
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)
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)
Mesitylation and phenylation of picolyl anions by the SRN1 mechanismJ. F. Bunnett, Bernhard F. Gloor; J. Org. Chem.; 1974; 39(3); 382-384.
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-3.pdf)
Arylation of several carbanions by the SRN1 mechanismRoberto A. Rossi and J. F. BunnettJournal of Organic Chemistry ,38,(17),pp 3020-3025 (1973)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-4.pdf)
SRN1 phenylation of nitrile carbanions and ensuing reactions. New route to alkylbenzenesJ. F. Bunnett and Bernhard F. GloorJournal of Organic chemistry, 38(24),pp 4156-4163 (1973)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/srn1.arylation-5.pdf)
Mesitylation and phenylation of picolyl anions by the SRN1 mechanismJ. F. Bunnett and Bernhard F. GloorJournal of Organic chemistry, 39(3), pp 382-384 (1974)
(
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 cleavageSatoshi Aoki, Tsutomu Fujimura, Eiichi Nakamura, Isao KuwajimaJ. Am. Chem. Soc. 110, 3296-3298 (1988)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/arylation.pd-triflate.pdf)
Ferrous ion catalysis of reactions of nucleophiles with aryl halidesCarlo Galli, J. F. BunnettJ. Org. Chem. 49, 3041-3042 (1984)
(
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.carbonyls-nitriles.html
Retrieved by ChemisTris:For Rhodium:Behavioral properties of psychoactive phenylisopropylamines in ratsEuropean Journal of Pharmacology 76(4), 353-360 (1981)
(
http://mishmashblue.tripod.com/euro.pdf)
Synthesis of MDP2P Synthetic Communications 24(2), 145 (1994)
(
http://mishmashblue.tripod.com/syncom.pdf)
For Vitus_Verdegast:Heterocycles 46, 91-94 (1997)
(
http://mishmashblue.tripod.com/heterocycles.djvu)
J. Nat. Prod. 60(11), 1196-98 (1997)
(
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 ColadoPharmacol. Rev., 5533-5600 (2003)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/mdma.pharmacology.pdf)
DOI:
10.1124/pr.55.3.3
Differences in potency and efficacy of a series of phenylisopropylamine/phenylethylamine pairs at 5-HT2A and 5-HT2C receptorsClaudio Acuña-Castillo, Claudio Villalobos, Pablo R. Moya, Patricio Sáez, Bruce K. Cassels, and J. Pablo Huidobro-ToroNone
(
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)
Retrieved by FreakyDMT:For Rhodium:10% Pd/C and HCOOH transfer hydrogenolysis of common protection groupsIndian journal of chemistry. Section B, 41(5):1064-1067 (2002)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/cth.protecting.group.removal.pdf)
Retrieved by Kinetic:For Chimimanie:Selective deprotection of esters using magnesium and methanolTet. Lett. 35(34), 6207-6210 (1994)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/ester.deprotection.mg-meoh.pdf)
DOI:
10.1016/S0040-4039(00)73392-2
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/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)
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)
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)
For Vitus-Verdegast:J. Pharm. Sci., 1967, 56, 970-973
(
http://lego.chemistry.tripod.com/Journals/TF-Amph.djvu)
(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)
(02-15-04):m- and
p-Hydroxy-1-cyanophenethylamine
Roger M. Pinder, Alfred Burger, E. J. Ariens
For AzoleSynthesis of Concave Receptors Derived from Diphenylglycoluril.
(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)
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)):
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. RasmussenJ. Med. Chem. 12, 919-921 (1969)
(
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-oxazolinesMichael R. Harnden, Ray R. RasmussenJ. Med. Chem. 13, 305-308 (1970)
(
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)
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)
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)
Retrieved by 7is:For Manichi:Binding of Phenylalkylamine Derivatives at 5-HT1C and 5-HT2 Serotonin Receptors: Evidence for a Lack of SelectivityRichard. A. GlennonJ. Med. Chem, 734 (1992)
(
http://nic-nac-project.de/~tajkor/jm00082a014.pdf)
The Ethyl Homologs of 2,4,5-TrimethoxyphenylisopropylaminesAlexander T. ShulginJ. Med. CHem 11, 196-187 (1968)
(
http://nic-nac-project.de/~tajkor/jm00307a056.pdf)
For Rhodium:Drug Discrimination and Receptor Binding Studies of N-Isopropyl Lysergamide DerivatesHuang, Marona-Lewicka, Pfaff, NicholsPharmacology, Biochmistry and Behavior 47(3), 667-673 (1994)
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/nichols/nichols-n-isopropyl-lysergamide.pdf)
Ergot Peptide Alkaloid Spectra of Claviceps-Infected Tall Fescue, Wheat, and BarleyJames 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)
Synthesis of some fluorinated nitro-olefinsR. 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)
DOI:
10.1016/0022-1139(93)02969-L
For PotterColour reactions of some aromatic ethers found in essential oilsJanet E. Forrest, R. Richard and R. A. HeacockJournal of Chromatography A, 65(2), 439-444 (1972)
(
http://nic-nac-project.de/~tajkor/18.pdf)
For Vitus1-EthynylphenethylamineAlfred Burger, Stuart E. Zimmerman, and E. J. AriënsJ. Med. Chem. 9, 469 (1966)
(
http://nic-nac-project.de/~tajkor/19.pdf)
For Ganesha: Forty years of hydride reductions
(03-19-04):Herbert C. Brown and S. KrishnamurthyTetrahedron 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 eugenolIndian Journal Of Chemistry. Sect. B. 42(2), 369-371 (2003)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/cu-cyclodextrin.eugenol.ox.djvu)
Zinc/hydrazine: A low cost-facile system for the reduction of nitro compoundsIndian Journal Of Chemistry. Sect. B. 42(1), 180-183 (2003)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/nitro2amine.zn-n2h4.djvu)
Reduction of oximes with NaBH4/CuSO4/MeOHIndian journal of chemistry. Section B, 41(5):1072-1074 (2002)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/oxime-reduction.nabh4-cuso4.djvu)
NaBH4/I2 reductive aminationIndian Journal of Chemistry Sect. B, 41(9), 1970-1971 (2002)
(
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-AcOHIndian Journal of Chemistry, Sect. B. 39(6), 403-405 (2000)
(
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 AlcoholsIndian Journal of Chemistry, Sect. B. 33, 182-183 (1994)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/aldehyde2alcohol.cocl2-zn-dmf-h2o.djvu)
Retrieved by Azole:For fallen_Angel:2,4,5-trimethoxybenzaldehyde from vanillinNone
(
http://hyperlab.0catch.com/J_Chem_Soc_C_2222.djvu)
pyrylium salts by Ac2O/HClO4 diacylation of olefinsNone
(
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)
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.
(03-09-04):H. G. H. ErdtmanNone
(
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.
(03-09-04):H. G. H. ErdtmanNone
(
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)
Diels-Alder route to precursors of anthranilic acid derivativesK. Gewald, None
(
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)
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)-aminomethylketonenK.Bodendorf, A.WalkArch. Pharm. (1961), 294 484-7
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/bodendorf.djvu)
None
(http://hyperlab.0catch.com/Derivati_Indolici_IV.djvu)None
(http://hyperlab.0catch.com/Derivati_Indolici_VI.djvu)None
(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)
For Ruthenium:The Reimer-Tiemann Reaction, Enhanced by Ultrasound
(03-15-04):John C. Cochran and Margaret G. MelvilleSynth. 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
(03-15-04):V. M. Rodionov, E. V. Machinskaya, and V. M. BelikovZh. 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.
(02-15-04):Sinhababu, A. K.; Borchardt, R. T.None
(
http://hyperlab.0catch.com/SynthCommun1982_12_983.djvu)
Selective ring C-methylation of hydroxybenzaldehydes via their Mannich bases.
(02-15-04):Sinhababu, A. K.; Borchardt, R. T.None
(
http://hyperlab.0catch.com/SynthCommun1983_13_677.djvu)
Alkene Reductions Employing Ethyl Acetate - Hydroxylamine, a Useful New Source of DiimideP. A. Wade, N. V. Amin
None
(
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)
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)
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)
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)
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)
Selective reduction of nitro compounds with titanium(II) reagents.J. George and S. Chandrasekaran
None
(
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)
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)
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.
(03-09-04):E. A. Karakhanov, A. Ya. Zhuchkova, T. Yu. Filippova, A. L. MaximovNone
(
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 O
2 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.
(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)
Indigo to alpha-Methyltryptamine
(03-09-04):S. Pietra and G. TacconiNone
(
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
)For Rhodium:The part that I copied before my money ran out for the xerox machine:5-Hydroxyvanillin to Myristicinaldehyde in 77% Yield
(03-09-04):Taniguchi, Eiji; Imamura, Keiichi; Ishabashi, Fumito; Matsui, Toshio; Nishio, AkiraAgric. Biol. Chem.; 53(3) 631-644 (1989)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/agrbiochem53-635-643.djvu)
Isomerization of some allylbenzenes in a microwave batch reactor
(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)
For Kinetic:Zinc chloride catalysed 2,2-dialkyl benzodioxole acylations with acetic anhydride, yields over 90%
(03-09-04):Indian J.Chem.Sect.B; 38; 2; 1999; 137 - 140.
(
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-dimethylphenylalaninesBeng 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)
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)
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)
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)
beta-Chloroethylamines related to mescalineCooper, Paul D.Journal of Medicinal Chemistry 16, 1057-9 (1973)
(
http://pharmacist.the-hive.tripod.com/meschalo.pdf)
Retrieved by Lugh:For Lego:New Sulfur Derivatives Of IndolesRocz. Chem.; 50; 1976; 603.
(
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 DiazoalkanenEugen Müller, Martin BauerNone
(
https://www.thevespiary.org/rhodium/Rhodium/pdf/diazomethane.ketone.homologation.pdf)
For Barium:The Darzen Condensation, Part IJ. Chem. Soc. C (1970), 1154
(
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)
Stereochemical Control of the Darzens CondensationJ.Chem. Soc., Chem. Commun. (1977), 902
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/jonczyk.djvu)
Synthesis of Glycidic esters in a two-phase solid-liquid systemSynth. Commun. (1982), 12, 355
(
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)
Structural Correlation between Apomorphine and LSD:
Involvement of Dopamine as well as Serotonin in the Actions of HallucinogenDave E. NicholsJ. Theor. Biol. 59, 167-177 (1976)
(
https://www.thevespiary.org/rhodium/Rhodium/djvu/nichols.djvu)
For Rhodium:Sodium borohydride: A versatile reagent in the reductive N-monoalkylation of
![](https://www.thevespiary.org/talk/Themes/default/images/ip.gif)
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