Preparation and Diastereoselective Birch Reduction-Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-ols

dc.contributor.authorArthur G. Schultz
dc.contributor.authorTimothy J. Guzi
dc.contributor.authorErika Larsson
dc.contributor.authorRainer Rahm
dc.contributor.authorKshitij Thakkar
dc.contributor.authorJean M. Bidlack1
dc.date.accessioned2012-11-14T15:18:33Z
dc.date.accessioned2025-02-17T14:01:19Z
dc.date.available2012-11-14T15:18:33Z
dc.date.issued2012-11-14
dc.descriptionPreparation and Diastereoselective Birch Reduction-Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-olsen_US
dc.description.abstractPreparation and Diastereoselective Birch Reduction-Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-olsen_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/4102
dc.language.isoenen_US
dc.subjectPreparation and Diastereoselective Birch Reduction-Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-olsen_US
dc.titlePreparation and Diastereoselective Birch Reduction-Alkylation of Chiral 3,4-Dihydro-1(2H)-isoquinolinones. Enantiospecific Syntheses and Opioid Receptor Affinities of Several Hydro-2,3- dimethyl-1H-7,12a-methanobenzo[6,7]cycloocta[1,2-c]pyridine-9-olsen_US
dc.typeArticleen_US

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