Highly Efficient Coupling of β-Substituted Aminoethane Sulfonyl Azides with Thio Acids, toward a New Chemical Ligation Reaction-Reference-Cited by-同舟云学术

Highly Efficient Coupling of β-Substituted Aminoethane Sulfonyl Azides with Thio Acids, toward a New Chemical Ligation Reaction

Published:2005-02-17 Issue:6 Volume:7 Page:1125-1128
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Merkx Remco¹,Brouwer Arwin J.¹,Rijkers Dirk T. S.¹,Liskamp Rob M. J.¹

Affiliation:

1. Department of Medicinal Chemistry, Faculty of Pharmaceutical Sciences, Utrecht Institute for Pharmaceutical Sciences, Utrecht University, P.O. Box 80082, 3508 TB Utrecht, The Netherlands

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol0501119

Reference25 articles.

1. Chemoselective Approaches to Glycoprotein Assembly

2. Azide-Alkyne Coupling: A Powerful Reaction for Bioconjugate Chemistry

3. Non-canonical amino acids in protein engineering

4. The Staudinger Ligation—A Gift to Chemical Biology

5. Chemoselective ligation reactions with proteins, oligosaccharides and cells

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