The Development of a Sulfamate-Tethered Aza-Michael Cyclization Allows for the Preparation of (−)-Negamycin <i>tert</i>-Butyl Ester-Reference-Cited by-同舟云学术

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The Development of a Sulfamate-Tethered Aza-Michael Cyclization Allows for the Preparation of (−)-Negamycin tert-Butyl Ester

Published:2024-04-10 Issue:8 Volume:89 Page:5911-5916
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Joshi Harshit¹,Nirpal Appasaheb K.¹,Paul Debobrata¹^ORCID,Kelley Steven P.²^ORCID,Mague Joel T.³,Sathyamoorthi Shyam¹^ORCID

Affiliation:

1. Department of Medicinal Chemistry, University of Kansas, Lawrence, Kansas 66047, United States

2. Department of Chemistry, University of Missouri─Columbia, Columbia, Missouri 65211, United States

3. Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, United States

Funder

National Institutes of Health

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00604

Reference39 articles.

1. Synthesis of 1,3-Difunctionalized Amine Derivatives through Selective C−H Bond Oxidation

2. Salient features of the aza-Wacker cyclization reaction

3. Modular Functionalization of Allenes to Aminated Stereotriads

4. A manganese catalyst for highly reactive yet chemoselective intramolecular C(sp3)–H amination

5. Sulfamyl Radicals Direct Photoredox-Mediated Giese Reactions at Unactivated C(3)–H Bonds

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