首页> 外文期刊>The Journal of Organic Chemistry >Efficient synthesis of 1,1'-binaphthyl and 2,2'-bi-o-tolyl-2,2'-bis(oxazoline)s and preliminary use for the catalytic asymmetric allylic oxidation of cyclohexene
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Efficient synthesis of 1,1'-binaphthyl and 2,2'-bi-o-tolyl-2,2'-bis(oxazoline)s and preliminary use for the catalytic asymmetric allylic oxidation of cyclohexene

机译:1,1'-联萘基和2,2'-双邻甲苯基-2,2'-双(恶唑啉)的高效合成及其在环己烯催化不对称烯丙基氧化中的初步应用

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摘要

Chiral C_2-symmetric bis(oxazoline)s have been usc- cessfully employed as ligands with various metals in numerous catalytic asymmetric processes. These include cyclopropanation, aziridination, allylic substitution, hydrosilylation, imine additions, Diels-Alder aldol, and Wacker-type cyclization reaction. In addition we and Pfalitz have recently used bis(oxazolne) copper complexes as catalysts for the asymmetric allylic oxida- tion of simple olefins using tert-butyl perbenzoate.
机译:在许多催化不对称过程中,手性C_2对称双(恶唑啉)已成功用作各种金属的配体。这些包括环丙烷化,叠氮化,烯丙基取代,氢化硅烷化,亚胺添加,Diels-Alder aldol和Wacker型环化反应。此外,我们和Pfalitz最近已使用双(恶唑烷)铜络合物作为催化剂,使用过苯甲酸叔丁酯对简单烯烃进行不对称烯丙基氧化。

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