摘要
Acid catalyzed rearrangements of 1 and 3 were examined. The olefinic double bond was the most reactive group in protonation reaction. In the absence of olefinic double bond, tert-hydroxy group reacted faster than cyclopropane ring.
Acid catalyzed rearrangements of 1 and 3 were examined. The olefinic double bond was the most reactive group in protonation reaction. In the absence of olefinic double bond, tert-hydroxy group reacted faster than cyclopropane ring.
