Synthesis of N‑Sulfinyl Sulfoximines from 5‑(Sulfoximido)dibenzothiophenium Triflates and Sodium Sulfinates
A transition-metal-free and efficient S–O/S–N bond interconversion reaction has been developed. The protocol facilitates an efficient synthesis of N-sulfinyl sulfoximines by reacting sulfoximido-substituted sulfonium salts with a wide range of sodium sulfinates, featuring broad substrate scope, incl...
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Published in | Journal of organic chemistry Vol. 89; no. 14; pp. 10311 - 10315 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
WASHINGTON
American Chemical Society
19.07.2024
Amer Chemical Soc |
Subjects | |
Online Access | Get full text |
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Summary: | A transition-metal-free and efficient S–O/S–N bond interconversion reaction has been developed. The protocol facilitates an efficient synthesis of N-sulfinyl sulfoximines by reacting sulfoximido-substituted sulfonium salts with a wide range of sodium sulfinates, featuring broad substrate scope, including a plethora of heterocyclic and fluoroalkyl substrates, high functional group tolerance, and mild conditions. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0022-3263 1520-6904 1520-6904 |
DOI: | 10.1021/acs.joc.4c01212 |