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.
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.

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.

Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity
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.
English
Total Synthesis of (±)-Calanolide A and Its Anti-HIV Activity
Abstract:
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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Key words:
- total synthesis
- / (±)-calanolide A
- / anti-HIV activity

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