Department of Chemistry, University of Michigan, Ann Arbor, MI 48109 (USA).
Angew Chem Int Ed Engl. 2013 Dec 2;52(49):12932-6. doi: 10.1002/anie.201304298. Epub 2013 Oct 9.
In control: A chiral phosphoric acid catalyst significantly enhances or completely overrides the inherent regioselective acetalization profiles exhibited by monosaccharide-derived 1,2-diol substrates. This study represents the first example of chiral-catalyst-directed regio- and enantioselective intermolecular acetalizations, which are complementary to existing methods for substrate-controlled functionalization of polyols.
手性磷酸催化剂显著增强或完全改变了单糖衍生的 1,2-二醇底物所表现出的固有区域选择性缩醛化特征。本研究代表了首例手性催化剂导向的区域和对映选择性的分子间缩醛化反应,与现有多元醇的底物控制功能化方法互补。