Asymmetric synthesis of 3,4-anti- and 3,4-syn-substituted aminopyrrolidines via lithium amide conjugate addition-Reference-Cited by-同舟云学术

Asymmetric synthesis of 3,4-anti- and 3,4-syn-substituted aminopyrrolidines via lithium amide conjugate addition

Published:2007 Issue:12 Volume:5 Page:1961
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Davies Stephen G.,Garner A. Christopher,Goddard Euan C.,Kruchinin Dennis,Roberts Paul M.,Smith Andrew D.,Rodriguez-Solla Humberto,Thomson James E.,Toms Steven M.

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2007/OB/B704932C

Reference70 articles.

1. A Diastereoselective Synthesis of 2,4-Disubstituted Piperidines: Scaffolds for Drug Discovery

2. Highly Diastereoselective and Enantioselective Carbon−Carbon Bond Formations in Conjugate Additions of Lithiated N-Boc Allylamines to Nitroalkenes: Enantioselective Synthesis of 3,4- and 3,4,5-Substituted Piperidines Including (−)-Paroxetine

3. Synthesis and biological activity of pyrrole, pyrroline and pyrrolidine derivatives with two aryl groups on adjacent positions

4. Asymmetric routes to substituted piperidines

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