Your browser doesn't support javascript.
loading
Asymmetric total synthesis of (+)-crassalactone D.
Yang, Zhicai; Tang, Phung; Gauuan, Jolicia F; Molino, Bruce F.
Affiliation
  • Yang Z; Medicinal Chemistry Department, AMRI, 26 Corporate Circle, P.O. Box 15098, Albany, New York 12212-5098, USA. zhicai.yang@amriglobal.com
J Org Chem ; 74(24): 9546-9, 2009 Dec 18.
Article in En | MEDLINE | ID: mdl-19924876
The asymmetric total synthesis of (+)-crassalactone D (4), a naturally occurring antitumor agent, has been achieved by employing an oxidative spirocyclization of furan 11 as the key step. Two close analogues, 7-epi-crassalactone D (14) and 5-epi-7-epi-crassalactone D (15), also have been prepared in the course of the synthesis of (+)-crassalactone D.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spiro Compounds / Furans / Antineoplastic Agents, Phytogenic Language: En Journal: J Org Chem Year: 2009 Document type: Article Affiliation country: United States Country of publication: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Spiro Compounds / Furans / Antineoplastic Agents, Phytogenic Language: En Journal: J Org Chem Year: 2009 Document type: Article Affiliation country: United States Country of publication: United States