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首页> 外文期刊>Tetrahedron >Facile and practical enantioselective synthesis of propargylic alcohols by direct addition of alkynes to aldehydes catalyzed by chiral disulfide-oxazolidine ligands
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Facile and practical enantioselective synthesis of propargylic alcohols by direct addition of alkynes to aldehydes catalyzed by chiral disulfide-oxazolidine ligands

机译:通过将炔烃直接添加到手性二硫化物-恶唑烷配体催化的醛中,炔醇的简便实用的对映选择性合成

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摘要

The enantioselective alkynylation reaction of aldehydes with alkynes and diethylzinc, catalyzed by chiral disulfide-oxazolidine ligands, provides a simple, practical and inexpensive method to access chiral propargylic alcohols in good yields and satisfactory ee's. (C) 2002 Elsevier Science Ltd. All rights reserved. [References: 29]
机译:手性二硫化物-恶唑烷配体催化的醛与炔烃和二乙基锌的对映选择性炔基化反应提供了一种简单,实用,廉价的方法,以高收率和令人满意的ee收率获得手性炔丙醇。 (C)2002 Elsevier ScienceLtd。保留所有权利。 [参考:29]

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