Regioselective Formation, Using Orthogonal Cysteine Protection, of an α-Conotoxin Dimer Peptide Containing Four Disulfide Bonds-Reference-Cited by-同舟云学术

Regioselective Formation, Using Orthogonal Cysteine Protection, of an α-Conotoxin Dimer Peptide Containing Four Disulfide Bonds

Published:2003-07-08 Issue:16 Volume:5 Page:2955-2957
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Cuthbertson Alan¹,Indrevoll Bård¹

Affiliation:

1. Amersham Health AS, Department of Medicinal Chemistry, Oslo, Norway

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/ol035105w

Reference11 articles.

1. (a) Doherty-Kirby, A.; Lojoie, G. A. InSolid-Phase Synthesis. APractical Guide; Kates, S. A., Albericio, F., Eds.; Marcel Dekker: New York, 2000; pp 129−176.

2. (b) Annis, I.; Hargittai, B.; Barany, G. InMethods inEnzymology; Fields, G. B., Ed.; 1997; Vol. 289, pp 198−221.

3. Molecular structure of the toxin domain of heat-stable enterotoxin produced by a pathogenic strain of Escherichia coli. A putative binding site for a binding protein on rat intestinal epithelial cell membranes.

4. The Tertiary Butyl Group as a Blocking Agent for Hydroxyl, Sulfhydryl and Amido Functions in Peptide Synthesis

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