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Chin. J. Org. Chem. ›› 1983, Vol. 3 ›› Issue (6): 440-442. Previous Articles Next Articles
吴碧琪;张联;周维善
发布日期:
WU BIQI;ZHANG LIAN;ZHOU WEISHAN
Published:
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The asymmetric epoxidation of three allylic alcohols (1-3) are described. The enantiomeric excess of the epoxyalcohol (obtained from the trans-allylic alcohol 2) was greater than that from the cis-allylic alcohol. The asymmetric epoxidation of the tertiary allylic alcohol yielded epoxy alcohol, of which the enantiomeric excess was only 4%.
Key words: EPOXIDATION REACTION, ENANTIOMORPH, PROPENOL
CLC Number:
O629
WU BIQI;ZHANG LIAN;ZHOU WEISHAN. Asymmetric epoxidations of allylic alcohols[J]. Chin. J. Org. Chem., 1983, 3(6): 440-442.
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