Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5279079 | Tetrahedron Letters | 2006 | 5 Pages |
Abstract
Candida antarctica lipase-catalyzed hydrolysis of O-butyryl-BINOL [(±)-3] or O-butyryl-6,6â²-dibromo-BINOL [(±)-5] yielded optically active BINOL [(R)-1] or 6,6â²-dibromo-BINOL [(R)-4] with high enantiomeric excess at 80 °C. Reaction temperature and acyl group of substrate had a great influence on the reactivity and enantioselectivity, respectively, of lipase-catalyzed hydrolysis for chiral binaphthol synthesis.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Naoto Aoyagi, Naomi Ogawa, Taeko Izumi,