Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity

Chun Mei ZHOU Lin WANG Ming Long ZHANG Zhi Zhong ZHAO Xing Quan ZHANG Xiang Hong CHEN Hong Shan CHEN

引用本文: Chun Mei ZHOU,  Lin WANG,  Ming Long ZHANG,  Zhi Zhong ZHAO,  Xing Quan ZHANG,  Xiang Hong CHEN,  Hong Shan CHEN. Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity[J]. Chinese Chemical Letters, 1998, 9(5): 433-434. shu
Citation:  Chun Mei ZHOU,  Lin WANG,  Ming Long ZHANG,  Zhi Zhong ZHAO,  Xing Quan ZHANG,  Xiang Hong CHEN,  Hong Shan CHEN. Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity[J]. Chinese Chemical Letters, 1998, 9(5): 433-434. shu

Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity

  • 基金项目:

    The authors are very grateful to Professor Xiao Tian Liang for his helpful suggestions and discussions, and thank the National Natural Science Foundation of China (No. 29772085) for financial support.

摘要: Anti-HIV agent (±)-calanolide A has been synthesized by a four-step approach starting from phloroglucinol, including the Pechmann reaction, Friedel-Crafts acylation, cyclization, chromenylation and Luche reduction.

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  • 收稿日期:  1997-11-10
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