分子内力
芳基
化学
磺胺
药物化学
立体化学
有机化学
烷基
作者
Chada Raji Reddy,Anjali Rathaur,Banoth Karuna Sagar
标识
DOI:10.1021/acs.joc.4c01517
摘要
Herein, we report acid-mediated divergent annulations of (N-aryl)-alkynyl sulfonamides. The substituent at the para position of the N-aryl group determines two diverse reaction paths, leading to the selective assembly of benzo-fused sultams and spirocyclic sultams. This strategy provides a series of benzo/spiro-sultams with wide functional group compatibility and good to excellent yields under mild reaction conditions. Additionally, scale-up reaction and further transformations of the products were also carried out to demonstrate the utility of the protocol.
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