期刊
TETRAHEDRON-ASYMMETRY
卷 25, 期 6-7, 页码 479-484出版社
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.tetasy.2014.03.002
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资金
- National Research Foundation of Korea Grant-Korean Government [2011-0010550]
- National Research Foundation of Korea [2011-0010550] Funding Source: Korea Institute of Science & Technology Information (KISTI), National Science & Technology Information Service (NTIS)
Asymmetric hydrosilylation of styrenes with trichlorosilane catalyzed by palladium complexes coordinated with chiral monodentate phosphorus ligands produces chiral benzylic silanes, which can be converted into enantiomerically enriched benzylic alcohols by a stereospecific oxidative cleavage of the carbon silicon bond with retention of configuration. Due to its high catalytic activity and perfect reg-ioselectivity without producing any by-products, it has recently become a potent methodology to prove the efficacy of newly-developed chiral ligands, especially monodentate ones, in asymmetric synthesis. (c) 2014 Elsevier Ltd. All rights reserved.
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