Solvolysis of 1-methylspiro[5, 2] octan-4-ols, 1–3, in acidified THF-90% H2O2 through a combination of cyclopropylcarbinyl and Criegee rearrangements constitutes a new stereoselective synthesis of 3-alkyl-4-hydroxycyclooctanones.
1-甲基螺[5,2]辛-4-醇的溶剂分解,1 - 3,在酸化的THF-90%H 2 ö 2通过cyclopropylcarbinyl和Criegee重排的组合构成的一个新的立体有择合成的3-烷基-
4-羟基
环辛酮。