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Preparation of cyclopropanone 2,2,2-trifluoroethoxy hemiacetals via oxyallyl cation
(ARKAT USA, Inc., 2024)
Hemiacetals of cyclopropanone can be isolated and stocked, contrary to their highly reactive parent ketone. However, they are not readily converted to cyclopropanone, which limits their use as its synthetic equivalents. ...