Stereoselective construction of the tetracyclic core of Cryptotrione
文献类型:期刊论文
作者 | Chen, Song1; Rong, Chao1; Feng, Pengju1; Li, Songlei1; Shi, Yian1,2 |
刊名 | ORGANIC & BIOMOLECULAR CHEMISTRY
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出版日期 | 2012 |
卷号 | 10期号:29页码:5518-5520 |
ISSN号 | 1477-0520 |
DOI | 10.1039/c2ob25923k |
英文摘要 | An efficient stereoselective approach to the tetracyclic core of Cryptotrione, involving an asymmetric Michael addition, ring-closing metathesis, and subsequent cyclopropanation, is described. |
语种 | 英语 |
WOS记录号 | WOS:000305965400004 |
出版者 | ROYAL SOC CHEMISTRY |
源URL | [http://ir.iccas.ac.cn/handle/121111/47935] ![]() |
专题 | 中国科学院化学研究所 |
通讯作者 | Shi, Yian |
作者单位 | 1.Chinese Acad Sci, Beijing Natl Lab Mol Sci, CAS Key Lab Mol Recognit & Funct, Inst Chem, Beijing 100190, Peoples R China 2.Colorado State Univ, Dept Chem, Ft Collins, CO 80523 USA |
推荐引用方式 GB/T 7714 | Chen, Song,Rong, Chao,Feng, Pengju,et al. Stereoselective construction of the tetracyclic core of Cryptotrione[J]. ORGANIC & BIOMOLECULAR CHEMISTRY,2012,10(29):5518-5520. |
APA | Chen, Song,Rong, Chao,Feng, Pengju,Li, Songlei,&Shi, Yian.(2012).Stereoselective construction of the tetracyclic core of Cryptotrione.ORGANIC & BIOMOLECULAR CHEMISTRY,10(29),5518-5520. |
MLA | Chen, Song,et al."Stereoselective construction of the tetracyclic core of Cryptotrione".ORGANIC & BIOMOLECULAR CHEMISTRY 10.29(2012):5518-5520. |
入库方式: OAI收割
来源:化学研究所
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