Total Synthesis of (±)-Cordatolide A and its Anti-HIV Activity 被引量：1

Total Synthesis of (±)-Cordatolide A and its Anti-HIV Activity

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摘要 The natural product (±)-cordatolide A has been synthesized by a four-step approach starting from phloroglucinol, including Pechmann reaction, Friedel-Crafts acylation, cyclization. chromenylation and Luche reduction. The natural product (±)-cordatolide A has been synthesized by a four-step approach starting from phloroglucinol, including Pechmann reaction, Friedel-Crafts acylation, cyclization. chromenylation and Luche reduction.

作者 Qi GAO Lin WANG Xiao Tian LIANG (Institute of Materia Medica, Peking Union Medical College & Chinese Academy of Medical Sciences, Beijing 100050)

出处《Chinese Chemical Letters》 SCIE CAS CSCD 1999年第8期653-656,共4页 中国化学快报（英文版）

关键词 Total synthesis (±)-cordatolide A Total synthesis， (±)-cordatolide A

分类号 O621 [理学—有机化学]

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Chinese Chemical Letters

1999年第8期

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Total Synthesis of (±)-Cordatolide A and its Anti-HIV Activity 被引量：1

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