Applications of tert-butanesulfinamide in the synthesis of N-heterocycles via sulfinimines. Issue 69 (23rd November 2020)

• Record Type: Journal Article
• Authors: Philip, Rose Mary; Radhika, Sankaran; Saranya, P. V.; Anilkumar, Gopinathan
• Is Part Of: RSC advances. Volume 10:Issue 69(2020)
• Page Start: 42441
• Page End: 42456
• Publication Date: 2020-11-23
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/d0ra08819f
• Languages: English
• ISSNs: 2046-2069

Abstract

Abstract : The review summarizes the usage of tert -butanesulfinamide for the construction of diverse N-heterocycles through sulfinimine intermediate over the last decade. Abstract : Chiral sulfinamides are among the best known chiral auxiliaries in the stereoselective synthesis of amines and their derivatives. The most extensively used enantiopure tert -butanesulfinamide emerged as the gold standard among many others over the last two decades. The present review attempts to provide an overview of tert -butanesulfinamide mediated asymmetric N-heterocycle synthesis via sulfinimines and covers literature from 2010–2020. This methodology offers general access to structurally diverse piperidines, pyrrolidines, azetidines, and their fused derivatives that represent the structural motif of many natural products and therapeutically applicable compounds.