Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1252925 | Chemical Research in Chinese Universities | 2008 | 4 Pages |
Abstract
Several borohydride reagents: sodium borohydride, sodium cyanoborohydride, soudium acetoxyborohydride and soudium triacetoxyborohydride were screened, respectively, for the reduction of 7-demethylsinomenine, which was an α,β-dicarbonyl compound derived from sinomenine. Highly regio- and stereo-selectivity was acquired when sodium cyanoborohydride or NaBH(OAc)3 was used. The product was structurally confirmed as 7R configuration by NMR, X-ray crystal diffraction analysis. Some preliminary discussion was also made on the mechanism of the selective reduction.
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Authors
Yu-feng LI, Qing-min BU, Yi QIAN, Yi PAN, Jian-xin LI, Le-qun HUANG, Hong-jun ZHU,