4.4 Article Proceedings Paper

α-Haloarylsulfonamides: multiple cyclization pathways to skeletally diverse benzofused sultams

期刊

TETRAHEDRON
卷 65, 期 16, 页码 3180-3188

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PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tet.2008.11.053

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  1. NCRR NIH HHS [P20 RR015563-076479, P20 RR015563] Funding Source: Medline
  2. NIGMS NIH HHS [P41 GM076302-02, P50 GM069663-05, P50 GM069663-04, P41 GM076302-03, P41 GM076302-01, P50 GM069663, P41 GM076302] Funding Source: Medline

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The development of new methods to skeletally diverse sultams based oil a central alpha-halo benzene sulfonamide building block is reported. Several salient features of this building block are Utilized ill multiple reaction pathways, including the Fleck reaction, C- and O-arylation, Sonogashira-Pauson-Khand, Sonogashira-intramolecular hydroamination, and domino aza-Michael-Heck for the generation of five-, six-, and seven-membered benzofused bicyclic and tricyclic sultams. (C) 2008 Elsevier Ltd. All rights reserved.

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