Highly stereoselective synthesis of cyclopropyl heterocycles via cyclopropanation of olefin with arsonium salt
β Scribed by Zhongjiao Ren; Weiguo Cao; Weiqi Tong; Jie Chen; Changqing Wang
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2008
- Tongue
- English
- Weight
- 411 KB
- Volume
- 45
- Category
- Article
- ISSN
- 0022-152X
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β¦ Synopsis
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.
π SIMILAR VOLUMES
## 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
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