3-Alkenyl-oxindoles: Natural Products, Pharmaceuticals, and Recent Synthetic Advances in Tandem/Telescoped Approaches

被引:327
|
作者
Millemaggi, Alessia [1 ]
Taylor, Richard J. K. [1 ]
机构
[1] Univ York, Dept Chem, York YO10 5DD, N Yorkshire, England
基金
英国工程与自然科学研究理事会;
关键词
Nitrogen heterocycles; Natural products; Antitumor agents; Domino reactions; Telescoped reactions; PALLADIUM-CATALYZED CYCLIZATION; C-H FUNCTIONALIZATION; PROTEASOME INHIBITORS TMC-95A; DEPENDENT KINASE INHIBITORS; STEREOSELECTIVE-SYNTHESIS; SELECTIVE SYNTHESIS; OXINDOLE ALKALOIDS; CELL-CYCLE; 2-(ALKYNYL)ARYL ISOCYANATES; 2-OXINDOLE DERIVATIVES;
D O I
10.1002/ejoc.201000643
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
The structures and biological activities of naturally occurring 3-alkenyl-oxindoles are reviewed. Important man-made 3-alkenyl-oxindoles are covered, particularly those with pharmaceutical applications such as sunitinib (SU11248), the orally active receptor tyrosine kinase inhibitor marketed by Pfizer as Sutent (R). Traditional synthetic approaches to 3-alkenyl-oxindoles are summarised and then recently developed tandem/telescoped synthetic routes are described.
引用
收藏
页码:4527 / 4547
页数:21
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