Organic letters

A novel, expeditious synthesis of racemic camptothecin

RJ Anderson, GB Raolji, A Kanazawa…

Index: Anderson, Regan J.; Raolji, Gajendra B.; Kanazawa, Alice; Greene, Andrew E. Organic Letters, 2005 , vol. 7, # 14 p. 2989 - 2991

Full Text: HTML

Citation Number: 38

Abstract

Isolated from the Chinese plant Camptotheca acuminata by Wall and co-workers in 1966, camptothecin (1) elicited widespread interest due to its potent antitumor activity. 1,2 The initial excitement quickly waned, however, because of problems associated with its insolubility and toxicity. Several years later, 3 though, it was reported that camptothecin had a unique mechanism of action that involved selective inhibition of DNA topoisomerase I. This disclosure served to rekindle interest in ...

Related Articles:

Total synthesis of dl-camptothecin

[Journal of the American Chemical Society, , vol. 97, p. 159 - 167]

Concise total syntheses of dl-camptothecin and related anticancer drugs

[Shen, Wang; Coburn, Craig A.; Bornmann, William G.; Danishefsky, Samuel J. Journal of Organic Chemistry, 1993 , vol. 58, # 3 p. 611 - 617]

Plant antitumor agents. 18. Synthesis and biological activity of camptothecin analogs

[Journal of Medicinal Chemistry, , vol. 23, # 5 p. 554 - 560]

A Six-Step Synthesis of (.+-.)-Camptothecin

[Comins, Daniel L.; Hong, Hao; Saha, Jayanta K.; Jianhua, Gao Journal of Organic Chemistry, 1994 , vol. 59, # 18 p. 5120 - 5121]

A novel, expeditious synthesis of racemic camptothecin

[Organic Letters, , vol. 7, # 14 p. 2989 - 2991]

More Articles...