Tetrahedron Letters p. 433 - 436 (1997)
Update date:2022-09-26
Topics:
Taniguchi, Takahiko
Ogasawara, Kunio
The Katsuki-Sharpless asymmetric epoxidation reaction of meso syn-2,3-bis-endo- and exo-allyl alcohols on a bicyclo[2.2.1]heptane framework took place regio- and stereo-selectively in a unilateral way to give the corresponding mono-epoxidation products as the major product.
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