<i>N</i>-to-<i>S</i> Acyl Transfer as an Enabling Strategy in Asymmetric and Chemoenzymatic Synthesis-Reference-Cited by-同舟云学术

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N-to-S Acyl Transfer as an Enabling Strategy in Asymmetric and Chemoenzymatic Synthesis

Published:2024-05-09 Issue:5 Volume:4 Page:2058-2066
ISSN:2691-3704
Container-title:JACS Au
language:en
Short-container-title:JACS Au

Author:

Jo Woonkee S.¹,Curtis Brian J.²,Rehan Mohammad¹,Adrover-Castellano Maria L.²,Sherman David H.²³^ORCID,Healy Alan R.¹^ORCID

Affiliation:

1. Chemistry Program, New York University Abu Dhabi (NYUAD), Saadiyat Island, Abu Dhabi 129188, United Arab Emirates (UAE)

2. Life Sciences Institute, University of Michigan, 210 Washtenaw Avenue, Ann Arbor, MI 48109, USA

3. Departments of Medicinal Chemistry, Chemistry, and Microbiology & Immunology, University of Michigan, Ann Arbor, MI 48109USA

Funder

Common Fund

New York University Abu Dhabi

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/jacsau.4c00257

Reference85 articles.

1. The ubiquitous carrier protein—a window to metabolite biosynthesis

2. Exploring chemoselective S-to-N acyl transfer reactions in synthesis and chemical biology

3. Synthesis of Proteins by Native Chemical Ligation

4. Sulfonyl Chlorides as Thiol Surrogates for Carbon–Sulfur Bond Formation: One-Pot Synthesis of Thioethers and Thioesters

5. Metal-Catalyzed Synthesis and Use of Thioesters: Recent Developments

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