4.8 Article

Synthesis of Indolines and Derivatives by Aza-Heck Cyclization

期刊

ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 58, 期 38, 页码 13448-13451

出版社

WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.201907758

关键词

aza-Heck reaction; catalysis; cyclization; indolines; palladium

资金

  1. University of Delaware (UD)
  2. NIH NIGMS [NIH P20 GM104316]
  3. NIH [NIH P20 GM104316, P20 GM104316, P30 GM110758, S10 RR026962, S10 OD016267, NSF CHE-0421224, CHE-0840401, CHE-1229234, CHE-1048367]
  4. NATIONAL INSTITUTE OF GENERAL MEDICAL SCIENCES [P30GM110758, P20GM104316] Funding Source: NIH RePORTER

向作者/读者索取更多资源

For the first time, an aza-Heck cyclization that allows the preparation of indoline scaffolds is described. Using N-hydroxy anilines as electrophiles, which can be easily accessed from the corresponding nitroarenes, this method provides indolines bearing pendant functionality and complex ring topologies. Synthesis of challenging indolines, such as those bearing fully substituted carbon atoms at C2, is also possible using this method.

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