缩醛形成过程中手性识别的增强。
Increasing chiral recognition in acetal formation.
作者信息
Noe Christian R, Knollmüller Max, Jangg Edith, Gmeiner Günter P, Urban Ernst, Eppacher Simon
机构信息
Department of Medicinal Chemistry, University of Vienna, Vienna, Austria.
出版信息
Chirality. 2009 Apr;21(4):428-35. doi: 10.1002/chir.20609.
PMID:18655172
Abstract
The design of substituted lactols is described, which in their reaction with racemic alkyl aryl carbinols react preferentially with one of the enantiomers exhibiting selectivities up to 14:1.
摘要
本文描述了取代乳糖醇的设计，其在与外消旋烷基芳基甲醇的反应中，优先与对映体之一发生反应，选择性高达14:1。
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