Involudispirones A and B: Sesterterpenes Containing a Dispiro Ring from  Stahlianthus involucratus | Zendy

Li QiangMing | Zendy; Luo JianGuang | Zendy; Zhao HuiJun | Zendy; Yu WenYing | Zendy; Wang XiaoBing | Zendy; Yang MingHua | Zendy; Luo Jun | Zendy; Sun HongBin | Zendy; Chen YiJun | Zendy; Guo QingLong | Zendy; Kong LingYi | Zendy

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Involudispirones A and B: Sesterterpenes Containing a Dispiro Ring from Stahlianthus involucratus

Author(s) -

Li QiangMing,

Luo JianGuang,

Zhao HuiJun,

Yu WenYing,

Wang XiaoBing,

Yang MingHua,

Luo Jun,

Sun HongBin,

Chen YiJun,

Guo QingLong,

Kong LingYi

Publication year - 2015

Publication title -

asian journal of organic chemistry

Language(s) - English

Resource type - Journals

SCImago Journal Rank - 0.846

H-Index - 44

eISSN - 2193-5815

pISSN - 2193-5807

DOI - 10.1002/ajoc.201500360

Subject(s) - chemistry , stereochemistry , ring (chemistry) , hexadecane , rhizome , cytotoxic t cell , absolute configuration , organic chemistry , traditional medicine , biochemistry , in vitro , medicine

Involudispirones A ( 1 ) and B ( 2 ), a pair of cytotoxic sesterterpene stereoisomers containing a 1,2‐dioxadispiro[5.2.5.2]hexadecane ring, were isolated from the rhizomes of Stahlianthus involucratus . Their structures and absolute configurations were established on the basis of spectroscopic data and chemical conversion. Both 1 and 2 are cytotoxic.

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