A Silyl Sulfinylamine Reagent Enables the Modular Synthesis of Sulfonimidamides via Primary Sulfinamides
Author:
Affiliation:
1. Department of Chemistry, University of Oxford, Chemistry Research Laboratory, Mansfield Road, Oxford, OX1 3TA, U.K.
Funder
AstraZeneca
Novartis
Vertex Pharmaceuticals
UCB
Takeda Pharmaceutical Company
Defence Science and Technology Laboratory
Diamond Light Source
Pfizer
GlaxoSmithKline
China Scholarship Council
Janssen Pharmaceuticals
Syngenta International
Evotec
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.2c00347
Reference48 articles.
1. CLVI.—The preparation of compounds analogous in structure to sulphinic acids but containing p-toluenesulphonimido-groups in place of oxygen atoms. Phenyl- and methyl-p-toluenesulphonimido-sulphine-p-toluenesulphonylimines
2. Sulfonimidamides in Medicinal and Agricultural Chemistry
3. How do we address neglected sulfur pharmacophores in drug discovery?
4. Neglected sulfur(vi) pharmacophores in drug discovery: exploration of novel chemical space by the interplay of drug design and method development
5. Exploration of Novel Chemical Space: Synthesis and in vitro Evaluation of N-Functionalized Tertiary Sulfonimidamides
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