Organic Synthesis Methodology. Preparation and Diastereoselective Birch Reduction−Alkylation of 3-Substituted 2-Methyl-2,3-dihydroisoindol-1-ones
Author:
Affiliation:
1. Department of Chemistry, Rensselaer Polytechnic Institute, Troy, New York 12180-3590 guo@3dp.com
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/jo005693g
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4. Asymmetric Total Synthesis of (+)-Apovincamine and a Formal Synthesis of (+)-Vincamine. Demonstration of a Practical “Asymmetric Linkage” between Aromatic Carboxylic Acids and Chiral Acyclic Substrates
5. An enantioselective method for reductive alkylation of aromatic carboxylic acid derivatives. Examination of the factors that provide stereoselectivity
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