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Enantioselective Synthesis of Chiral Sulfinamidines via Asymmetric Amination of Sulfenamides Using a Chiral Phosphoric Acid Catalyst

Qi Chen, Chaoxiang Ning, Xuhao Ren, Xiaodong Xiong

2025Angewandte Chemie International Edition6 citationsDOIOpen Access PDF

Abstract

Despite the significant applications of stereogenic-at-sulfur compounds in pharmaceutical sciences and organic chemistry, efficient methods for precise construction of valuable chiral sulfinamidines remain limited. Herein, we disclosed a chiral phosphoric acid-catalyzed asymmetric strategy for the synthesis of chiral sulfinamidines through the direct amination of sulfenamides. This method demonstrated remarkable substrate scope and excellent yields and stereoselectivities across a diverse array of sulfinamidine compounds. The synthetic utility and practicability of this robust protocol were further highlighted through gram-scale reactions, product derivatization and late-stage functionalization of natural products and drugs.

Topics & Concepts

Enantioselective synthesisAminationChemistryPhosphoric acidCatalysisDerivatizationCombinatorial chemistryOrganic chemistryNatural productSubstrate (aquarium)Organic synthesisSurface modificationOrganocatalysisScope (computer science)Reaction conditionsStereoisomerismChiral derivatizing agentSynthesis and Catalytic ReactionsAsymmetric Hydrogenation and CatalysisSulfur-Based Synthesis Techniques
Enantioselective Synthesis of Chiral Sulfinamidines via Asymmetric Amination of Sulfenamides Using a Chiral Phosphoric Acid Catalyst | Litcius