In:
European Journal of Organic Chemistry, Wiley, Vol. 2017, No. 44 ( 2017-12), p. 6486-6490
Abstract:
NH‐sulfoximines are emerging as useful and important targets in drug discovery and synthetic organic chemistry. We report herein the development of an efficient, convenient, and sustainable continuous‐flow strategy, for the direct, straightforward preparation of NH‐sulfoximines by using sulfides or sulfoxides as suitable starting material. The flow process uses PhI(OAc) 2 as the oxidant and aqueous solutions of ammonia as the N source. The scope of the reaction has been demonstrated by using several substituted sulfides and sulfoxides including enantioenriched and biologically relevant starting materials. The flow strategy was found to be more convenient with respect to conventional batch processing.
Type of Medium:
Online Resource
ISSN:
1434-193X
,
1099-0690
DOI:
10.1002/ejoc.v2017.44
DOI:
10.1002/ejoc.201700850
Language:
English
Publisher:
Wiley
Publication Date:
2017
detail.hit.zdb_id:
1475010-7
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