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 inPost 217986 (https://www.thevespiary.org/talk/index.php?topic=11962.msg21798600#msg21798600)
(Rhodium: "Wanted references", Novel Discourse).Post 499541 (https://www.thevespiary.org/talk/index.php?topic=11630.msg49954100#msg49954100)
(Rhodium: "Archive of "Wanted References" Volume 2", Novel Discourse)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)
http://members.lycos.co.uk/chimimanie/chlorodifluoromethane.pdf (http://members.lycos.co.uk/chimimanie/chlorodifluoromethane.pdf)
http://members.lycos.co.uk/chimimanie/austjchem-777-1990.PDF (http://members.lycos.co.uk/chimimanie/austjchem-777-1990.PDF)
http://members.lycos.co.uk/chimimanie/BSCBelg977-1981.PDF (http://members.lycos.co.uk/chimimanie/BSCBelg977-1981.PDF)
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)10.1016/0091-3057(91)90601-W (http://dx.doi.org/10.1016/0091%2D3057%2891%2990601%2DW)
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)
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)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)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)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)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)10.1081/SCC-120005997 (http://dx.doi.org/10.1081/SCC%2D120005997)
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)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)Post 468717 (https://www.thevespiary.org/talk/index.php?topic=12405.msg46871700#msg46871700)
(Lego: "Amide to thioamide to amine", Serious Chemistry)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)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)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)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)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)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)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)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)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)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)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)Nature 221, 537-541 (1969) (https://www.thevespiary.org/rhodium/Rhodium/djvu/shulgins.djvu)
(https://www.thevespiary.org/rhodium/Rhodium/djvu/shulgins.djvu)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)
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")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)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)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)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)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)10.1021/jm9906062 (http://dx.doi.org/10.1021/jm9906062)
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)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)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)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)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)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)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)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)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)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)10.1016/S0273-1223(96)00704-4 (http://dx.doi.org/10.1016/S0273%2D1223%2896%2900704%2D4)
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)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)None (https://www.thevespiary.org/rhodium/Rhodium/pdf/beta-dichloroketones.pdf)
(https://www.thevespiary.org/rhodium/Rhodium/pdf/beta-dichloroketones.pdf)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)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)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)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)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)10.1016/0040-4039(95)00656-W (http://dx.doi.org/10.1016/0040%2D4039%2895%2900656%2DW)
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)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)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)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)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)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)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)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)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)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)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)
European Journal of Pharmacology 76(4), 353-360 (1981) (http://mishmashblue.tripod.com/euro.pdf)
(http://mishmashblue.tripod.com/euro.pdf)Synthetic Communications 24(2), 145 (1994) (http://mishmashblue.tripod.com/syncom.pdf)
(http://mishmashblue.tripod.com/syncom.pdf)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)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)10.1124/pr.55.3.3 (http://dx.doi.org/10.1124/pr.55.3.3)
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)Tetrahedron Letters 10(39), 3375-3376 (1969) (http://mishmashblue.tripod.com/isotryptamine.pdf)
(http://mishmashblue.tripod.com/isotryptamine.pdf)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)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)10.1016/S0040-4039(00)73392-2 (http://dx.doi.org/10.1016/S0040%2D4039%2800%2973392%2D2)
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)
Phytochemistry (Elsevier) (1981), 20(5), 1164-5. (http://lego.chemistry.tripod.com/Journals/1164.djvu)
(http://lego.chemistry.tripod.com/Journals/1164.djvu)Chemical & Pharmaceutical Bulletin (1980), 28(10), 2948-59 (http://lego.chemistry.tripod.com/Journals/2948.djvu)
(http://lego.chemistry.tripod.com/Journals/2948.djvu)Arzneimittel-Forschung (2001), 51(7), 535-544 (http://lego.chemistry.tripod.com/Journals/535.djvu)
(http://lego.chemistry.tripod.com/Journals/535.djvu)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) (02-15-04):Arzneimittel-Forschung , 1970, 20, 245-246 (http://lego.chemistry.tripod.com/Journals/CN-Amph.djvu)
(http://lego.chemistry.tripod.com/Journals/CN-Amph.djvu) (02-15-04):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)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)):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)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)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)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)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)J. Med. Chem, 734 (1992) (http://nic-nac-project.de/~tajkor/jm00082a014.pdf)
(http://nic-nac-project.de/~tajkor/jm00082a014.pdf)J. Med. CHem 11, 196-187 (1968) (http://nic-nac-project.de/~tajkor/jm00307a056.pdf)
(http://nic-nac-project.de/~tajkor/jm00307a056.pdf)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)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)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)10.1016/0022-1139(93)02969-L (http://dx.doi.org/10.1016/0022%2D1139%2893%2902969%2DL)
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)J. Med. Chem. 9, 469 (1966) (http://nic-nac-project.de/~tajkor/19.pdf)
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(http://hyperlab.0catch.com/JHetChem1980_17_985.djvu)(https://www.thevespiary.org/rhodium/Rhodium/hive/hiveboard/picproxie_imgs/djvu.gif)
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