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<i>tert</i>‐Butyl Hydroperoxide‐Initiated Radical Cyclization of 1‐(Allyloxy)‐2‐(1‐Arylvinyl)Benzenes with Sulfinic Acids to Access Sulfonated Benzoxepines

Nengneng Zhou, Kaimo Kuang, Meixia Wu, Sixin Wu, Qiankun Xu, Ziqin Xia, Man Zhang

2021Advanced Synthesis & Catalysis24 citationsDOI

Abstract

Abstract A tert ‐butyl hydroperoxide‐initiated radical cyclization of 1‐(allyloxy)‐2‐(1‐arylvinyl)benzenes with sulfinic acids for the construction of sulfonated benzoxepines is developed. This reaction involves a radical pathway and offers a straightforward route to the formation of seven‐membered ring via sulfonylation/cyclization process. This methodology features mild reaction conditions, a broad substrate scope and good functional group tolerance. magnified image

Topics & Concepts

ChemistrySulfinic acidSubstrate (aquarium)SulfonylScope (computer science)Ring (chemistry)Radical cyclizationFunctional groupOrganic chemistryCombinatorial chemistryPhotochemistryMedicinal chemistryGeologyPolymerOceanographyAlkylComputer scienceProgramming languageSulfur-Based Synthesis TechniquesRadical Photochemical ReactionsChemical Synthesis and Reactions
<i>tert</i>‐Butyl Hydroperoxide‐Initiated Radical Cyclization of 1‐(Allyloxy)‐2‐(1‐Arylvinyl)Benzenes with Sulfinic Acids to Access Sulfonated Benzoxepines | Litcius