Stereoselective synthesis of cyclopropyl indolyl ketones with indolylidene and arsonium ylide
β Scribed by Dong Zhou; Zhongjiao Ren; Weiguo Cao; Jie Chen; Ying Liu; Hongmei Deng; Min Shao
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2010
- Tongue
- English
- Weight
- 242 KB
- Volume
- 47
- Category
- Article
- ISSN
- 0022-152X
- DOI
- 10.1002/jhet.432
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β¦ Synopsis
Abstract
magnified image An efficient approach for stereoselective synthesis of cyclopropyl indolyl ketone from olefin and arsonium ylied was achieved. Its advantages are of mild condition, high yield, and good stereoselectivity. In addition, the oneβpot cycloproparation of olefins with bromides and triphenylarsine was studied. J. Heterocyclic Chem., (2010).
π SIMILAR VOLUMES
## Abstract magnified image An efficient and highly stereoselective approach for the preparation of highly functionalized cyclopropyl heterocycles __via__ the cyclopropanation of olefines with arsonium salts in the presence of KF2H~2~O has been developed.
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