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-Reference-Cited by-同舟云学术

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

Published:1998-10-01 Issue:22 Volume:63 Page:7795-7804
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Schultz Arthur G.¹,Guzi Timothy J.¹,Larsson Erika¹,Rahm Rainer¹,Thakkar Kshitij¹,Bidlack Jean M.¹

Affiliation:

1. Department of Chemistry, Rensselaer Polytechnic Institute, Troy, New York 12180-3590, and Department of Pharmacology, University of Rochester Medical Center, Rochester, New York 14642-8711

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo980921g

Reference32 articles.

1. Photoreduction de la benzophenone par des phtalimidines et des dihydro isoquinolones

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