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The Synthesis of Morphine
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This article has been cited by 8 ACS Journal articles (5 most recent appear below).

Concise Syntheses of (−)-Galanthamine and (±)-Codeine via Intramolecular Alkylation of a Phenol Derivative
Philip Magnus, Neeraj Sane, Benjamin P. Fauber and Vince LynchJournal of the American Chemical Society2009 131 (44), 16045-16047Concise Syntheses of (−)-Galanthamine and (±)-Codeine via Intramolecular Alkylation of a Phenol Derivative
Philip Magnus, Neeraj Sane, Benjamin P. Fauber and Vince LynchJournal of the American Chemical Society2009 131 (44), 16045-16047Suzuki coupling of 7 to 8 gave the biphenyl derivative 9. Reaction of 9 with ethyl vinyl ether/bromine/base gave 10, which on treatment with CsF/DMF at 130 °C resulted in the cross-conjugated 2,5-cyclohexadienone 6. Acid hydrolysis of 6 gave 11, which was ...

Lewis Acid Catalyzed Diels−Alder Reactions of 1,2-Naphthoquinones
Danny M. Gelman, Craig M. Forsyth and Patrick PerlmutterOrganic Letters2009 11 (21), 4958-4960Lewis Acid Catalyzed Diels−Alder Reactions of 1,2-Naphthoquinones
Danny M. Gelman, Craig M. Forsyth and Patrick PerlmutterOrganic Letters2009 11 (21), 4958-4960The use of BF3·OEt2 catalysis in Diels−Alder reactions of 3,4-unsubstituted 1,2-naphthoquinones provides direct access to cis-tetrahydrophenanthrene derivatives in good to excellent yields (66−99%) without rapid adduct aromatization commonly associated ...

Synthesis of an Estrogen Receptor β-Selective Radioligand: 5-[18F]Fluoro-(2R*,3S*)-2,3-bis(4-hydroxyphenyl)pentanenitrile and Comparison of in Vivo Distribution with 16α-[18F]Fluoro-17β-estradiol
Jeongsoo Yoo, Carmen S. Dence, Terry L. Sharp, John A. Katzenellenbogen, and Michael J. WelchJournal of Medicinal Chemistry2005 48 (20), 6366-6378Synthesis of an Estrogen Receptor β-Selective Radioligand: 5-[18F]Fluoro-(2R*,3S*)-2,3-bis(4-hydroxyphenyl)pentanenitrile and Comparison of in Vivo Distribution with 16α-[18F]Fluoro-17β-estradiol
Jeongsoo Yoo, Carmen S. Dence, Terry L. Sharp, John A. Katzenellenbogen, and Michael J. WelchJournal of Medicinal Chemistry2005 48 (20), 6366-6378Estrogen receptor (ER), a less active ER subtype that appears to have a restraining effect on the more active ER, could be a factor that determines the level of estrogen action in certain estrogen target tissues. ER is found in breast cancer, and its ...

Decoration of the Aromatic Ring of Dihydrocodeinone (Hydrocodone) and 14-Hydroxydihydrocodeinone (Oxycodone)
Michael L. Wilson, Patrick J. Carroll, and David R. DaltonThe Journal of Organic Chemistry2005 70 (16), 6492-6495Decoration of the Aromatic Ring of Dihydrocodeinone (Hydrocodone) and 14-Hydroxydihydrocodeinone (Oxycodone)
Michael L. Wilson, Patrick J. Carroll, and David R. DaltonThe Journal of Organic Chemistry2005 70 (16), 6492-6495Improved protocols for the preparation of 1-bromodihydrocodeinone (1-bromohydrocodone) and 1-bromo-14-hydroxydihydrocodeinone (1-bromooxycodone) and synthesis of the corresponding 1-chloro and 1-iodo derivatives have been achieved using the corresponding ...

4,5-Diphenyltriazol-3-ones: Openers of Large-Conductance Ca2+-Activated Potassium (Maxi-K) Channels
Jeffrey L. Romine, Scott W. Martin, Valentin K. Gribkoff, Christopher G. Boissard, Steven I. Dworetzky, Joanne Natale, Yi Li, Qi Gao, Nicholas A. Meanwell, and John E. Starrett, Jr.Journal of Medicinal Chemistry2002 45 (14), 2942-29524,5-Diphenyltriazol-3-ones: Openers of Large-Conductance Ca2+-Activated Potassium (Maxi-K) Channels
Jeffrey L. Romine, Scott W. Martin, Valentin K. Gribkoff, Christopher G. Boissard, Steven I. Dworetzky, Joanne Natale, Yi Li, Qi Gao, Nicholas A. Meanwell, and John E. Starrett, Jr.Journal of Medicinal Chemistry2002 45 (14), 2942-2952A series of diphenyl-substituted heterocycles were synthesized and evaluated by electrophysiological techniques as openers of the cloned mammalian large-conductance, Ca2+-activated potassium (maxi-K) channel. The series was designed from deannulation of ...
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- Published In Issue April, 1956
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