Phosphine-Dependent Photoinitiation of Alkyl Thiols under Near-UV Light Facilitates User-Friendly Peptide Desulfurization-Reference-Cited by-同舟云学术

Phosphine-Dependent Photoinitiation of Alkyl Thiols under Near-UV Light Facilitates User-Friendly Peptide Desulfurization

Published:2023-01-05 Issue:2 Volume:145 Page:1053-1061
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Venneti Naresh M.¹^ORCID,Samala Ganesh¹,Morsy Rana M. I.¹,Mendoza Lawrence G.¹,Isidro-Llobet Albert²^ORCID,Tom Janine K.³^ORCID,Mukherjee Subha⁴,Kopach Michael E.⁵^ORCID,Stockdill Jennifer L.¹^ORCID

Affiliation:

1. Department of Chemistry, Wayne State University, Detroit, Michigan 48202, United States

2. GlaxoSmithKline, Medicines Research Centre, Stevenage SG1 2NY, United Kingdom

3. Amgen, Inc., Pivotal Drug Substance Process Development, Thousand Oaks, California 91320, United States

4. Bristol-Myers Squibb, Chemical and Synthetic Development, New Brunswick, New Jersey 08903, United States

5. Eli Lilly and Company, Indianapolis, Indiana 46285, United States

Funder

Division of Chemistry

American Chemical Society

Wayne State University

National Institute of General Medical Sciences

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.2c10625

Reference45 articles.

1. Synthesis of Proteins by Native Chemical Ligation

2. Development of New Thioester Equivalents for Protein Chemical Synthesis

3. Native chemical ligation in protein synthesis and semi-synthesis

4. Advances in Native Chemical Ligation-Desulfurization: A Powerful Strategy for Peptide and Protein Synthesis

5. Expanding Native Chemical Ligation Methodology with Synthetic Amino Acid Derivatives

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