An Efficient Access to Enantiomerically Pure Substituted Derivatives of Pipecolic Acid-Reference-Cited by-同舟云学术

An Efficient Access to Enantiomerically Pure Substituted Derivatives of Pipecolic Acid

Published:2000-06-09 Issue:14 Volume:65 Page:4435-4439
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Agami Claude¹,Comesse Sébastien¹,Kadouri-Puchot Catherine¹

Affiliation:

1. Laboratoire de Synthèse Asymétrique (UMR CNRS 7611), Case courrier 47, Université P. et M. Curie, 4 place Jussieu, 75005 Paris, France kadouri@ccr.jussieu.fr

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo0000271

Reference17 articles.

1. An acyl-iminium ion cyclization route to a novel conformationally restricted dipeptide mimic: applications to angiotensin-converting enzyme inhibition

2. Selective inhibition of thrombin by (2R,4R)-4-methyl-1-[N2-[1,2,3,4-tetrahydro-8-quinolinyl)sulfonyl]-L-arginyl]-2-piperidinecarboxylic acid

3. Potent inhibition of thrombin by the newly synthesized arginine derivative No. 805. The importance of stereo-structure of its hydrophobic carboxamide portion

4. 35. The 4-hydroxypipecolic acid from acacia species, and its stereoisomers

5. Ruthenium-catalyzed ring closing olefin metathesis of non-natural α-amino acids

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