Litcius/Paper detail

Access to chiral β-sulfonyl carbonyl compounds <i>via</i> photoinduced organocatalytic asymmetric radical sulfonylation with sulfur dioxide

Fu‐Sheng He, Chun Zhang, Minghui Jiang, Lujun Lou, Jie Wu, Shengqing Ye

2022Chemical Science65 citationsDOIOpen Access PDF

Abstract

and α,β-unsaturated carbonyl compounds under photoinduced conditions is developed, which provides an efficient pathway for the synthesis of chiral β-sulfonyl carbonyl compounds in good yields with excellent enantioselectivity (up to 96% ee). Aside from α,β-unsaturated carbonyl compounds with auxiliary groups, common chalcone substrates are also well compatible with this organocatalytic system. This method proceeds through an organocatalytic enantioselective radical sulfonylation under photoinduced conditions, and represents a rare example of asymmetric transformation involving sulfur dioxide insertion.

Topics & Concepts

Enantioselective synthesisChemistrySulfonylOrganocatalysisChalconePhotochemistryOrganic chemistryCatalysisCombinatorial chemistryAlkylSulfur-Based Synthesis TechniquesRadical Photochemical ReactionsChemical Synthesis and Reactions