Stereocontrolled Formation of Ketomethylene Isosteres through Tandem Chain Extension Reactions-Reference-Cited by-同舟云学术

Stereocontrolled Formation of Ketomethylene Isosteres through Tandem Chain Extension Reactions

Published:2006-09-23 Issue:21 Volume:71 Page:8140-8145
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Lin Weimin¹,Tryder Nancy¹,Su Fan¹,Zercher Charles K.¹,Jasinski Jerry P.¹,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, 2400 Sixth Street, Washington, D.C. 20059

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/jo061184o

Reference32 articles.

1. Epoxyalcohol Route to Hydroxyethylene Dipeptide Isosteres. Stereodivergent Synthesis of the Diamino Alcohol Core of Ritonavir and Its C-2 Epimer

2. The discovery of structurally novel CCR1 antagonists derived from a hydroxyethylene peptide isostere template

3. A Stereocontrolled, Convergent Synthesis of Hydroxyethylene Dipeptide Isosteres

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

5. 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

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