【摘 要】
：
The total synthesis of (±)-abyssinoflavanone V was first achieved through C-prenylation, selective protection of phenolic hydroxyl group, aldol condensation, c
【机 构】
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Key Laboratory of Energy Sources and Chemical Engineering of Ningxia
【基金项目】
：
国家自然科学基金;教育部资助项目
论文部分内容阅读
The total synthesis of (±)-abyssinoflavanone V was first achieved through C-prenylation, selective protection of phenolic hydroxyl group, aldol condensation, cyclization and deprotection starting from cheap 4-hydroxybenzaldehyde and 2,4,6-trihydroxyacetophenone, with total yield 24%. All structures of new compounds were confirmed by IR, 1H NMR and MS.
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