Highly Enantioselective Addition of Phenylethynylzinc to Aldehydes Catalyzed by Chiral Cyclopropane-Based Amino Alcohols

Autor: Bing Zheng, Zhiyuan Li, Feipeng Liu, Yanhua Wu, Junjian Shen, Qinghua Bian, Shicong Hou, Ming Wang
Jazyk: angličtina
Rok vydání: 2013
Předmět:
Zdroj: Molecules, Vol 18, Iss 12, Pp 15422-15433 (2013)
Druh dokumentu: article
ISSN: 1420-3049
DOI: 10.3390/molecules181215422
Popis: The enantioselective addition of phenylethynylzinc to aldehydes catalyzed by a series of cyclopropane-based amino alcohol ligands 7 was investigated. The reactions afforded chiral propargylic alcohols in high yields (up to 96%) and with excellent enantioselectivities (up to 98% ee) under mild conditions. Furthermore, studies on the structural relationship show that the matching of the chiral center configuration is crucial to obtain the high enantioselectivity.
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