期刊论文详细信息
Molecules | |
Photochemical Aryl Radical Cyclizations toGive (E)-3-Ylideneoxindoles | |
Ingrid Allart-Simon1  Stéphane Gérard1  Janos Sapi1  Patrick McArdle2  Michael Gurry2  Fawaz Aldabbagh2  | |
[1] Institut de Chimie Moléculaire de Reims, UMR CNRS 7312, Université de Reims-Champagne-Ardenne, Faculté de Pharmacie, 51 rue Cognacq-Jay, F-51096 Reims Cedex, France;School of Chemistry, National University of Ireland Galway, University Road, Galway, Ireland; | |
关键词: cyclization; heterocycle; oxindole; UV-light; | |
DOI : 10.3390/molecules191015891 | |
来源: DOAJ |
【 摘 要 】
(E)-3-Ylideneoxindoles are prepared in methanol in reasonable to good yields, as adducts of photochemical 5-exo-trig of aryl radicals, in contrast to previously reported analogous radical cyclizations initiated by tris(trimethylsilyl)silane and azo-initiators that gave reduced oxindole adducts.
【 授权许可】
Unknown