Article ID Journal Published Year Pages File Type
5288485 Tetrahedron Letters 2005 4 Pages PDF
Abstract
The asymmetric reduction of benzophenones multisubstituted at the ortho-positions was achieved via hydrosilylation catalyzed by in situ generated chiral diamine-Zn-diol complexes under mild conditions, wherein polymethylhydrosiloxane (PMHS) served as a safe and inexpensive source of hydride.
Related Topics
Physical Sciences and Engineering Chemistry Organic Chemistry
Preview
Asymmetric reduction of ortho-multisubstituted benzophenones catalyzed by diamine-Zn-diol complexes
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