Unexpectedly Selective Formation and Reactions of Epoxycyclooctenones under Microwave-Mediated Conditions
收藏NIAID Data Ecosystem2026-03-06 收录
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资源简介：
Topologically mobile difluorinated cyclooctenones undergo rapid, high-yielding, and completely stereoselective epoxidations with methyl(trifluoromethyl)dioxirane. The epoxides resist conventional hydrolysis but react smoothly in basic media under microwave irradiation to afford unique hemiacetals and hemiaminals in good yield.
创建时间：
2004-04-15
