期刊
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
卷 132, 期 2, 页码 440-+出版社
AMER CHEMICAL SOC
DOI: 10.1021/ja9078094
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资金
- National Science Foundation [CHE-0907936]
- Direct For Mathematical & Physical Scien
- Division Of Chemistry [0907936] Funding Source: National Science Foundation
An effective Rh-2(S-DOSP)(4)-catalyzed asymmetric cyclopentannulation of indolyl rings has been developed. Depending on the Substitution pattern of the indole. two distinct regioisomeric products can be generated. These studies demonstrate that rhodium-catalyzed reactions of donor/acceptor carbenoids proceeding by means of zwitterionic intermediates can be carried out with very high asymmetric induction.
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