Stereoselective Formation of a Functionalized Dipeptide Isostere by Zinc Carbenoid-Mediated Chain Extension-Reference-Cited by-同舟云学术

Stereoselective Formation of a Functionalized Dipeptide Isostere by Zinc Carbenoid-Mediated Chain Extension

Published:2008-12-04 Issue:2 Volume:74 Page:645-651
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lin Weimin¹,Theberge Cory R.¹,Henderson Timothy J.¹,Zercher Charles K.¹,Jasinski Jerry¹,Butcher Ray. J.¹

Affiliation:

1. Department of Chemistry, University of New Hampshire, Durham, New Hampshire 03824, Department of Chemistry, Keene State College, 229 Main Street, Keene, New Hampshire 03435, and Department of Chemistry, Howard University, 525 College Street NW, Washington, D.C. 20059

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo801993k

Reference47 articles.

1. Methyl- and (Trifluoromethyl)alkene Peptide Isosteres: Synthesis and Evaluation of Their Potential as β-Turn Promoters and Peptide Mimetics

2. Diastereoselective Synthesis of New ψ[(E)-CHCMe]- and ψ[(Z)-CHCMe]-type Alkene Dipeptide Isosteres by Organocopper Reagents and Application to Conformationally Restricted Cyclic RGD Peptidomimetics

3. Electrostatic versus Steric Effects in Peptidomimicry: Synthesis and Secondary Structure Analysis of Gramicidin S Analogues with (E)-Alkene Peptide Isosteres

4. A Silanediol Inhibitor of the Metalloprotease Thermolysin: Synthesis and Comparison with a Phosphinic Acid Inhibitor1

5. Silanediol-Based inhibitor of thermolysin

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