中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
A highly alpha-regioselective AgOTf-catalyzed nucleophilic substitution of the Baylis-Hillman acetates with indoles

文献类型:期刊论文

作者Shafiq, Zahid; Liu, Li; Liu, Zhe; Wang, Dong; Chen, Yong-Jun
刊名ORGANIC LETTERS
出版日期2007-06-21
卷号9期号:13页码:2525-2528
ISSN号1523-7060
DOI10.1021/ol070878w
英文摘要An efficient method for highly alpha-regioselective nucleophilic substitution of the Baylis-Hillman acetates with indoles catalyzed by AgOTf in high yields (72-99%) has been developed. Reductive cyclization of the substitution products furnished the azepinoindole derivatives in good yields (up to 93%).
语种英语
WOS记录号WOS:000247215700025
出版者AMER CHEMICAL SOC
源URL[http://ir.iccas.ac.cn/handle/121111/60579]  
专题中国科学院化学研究所
通讯作者Shafiq, Zahid
作者单位Chinese Acad Sci, Inst Chem, Beijing Natl Lab Mol Sci, Lab Chem Biol, Beijing 100080, Peoples R China
推荐引用方式
GB/T 7714
Shafiq, Zahid,Liu, Li,Liu, Zhe,et al. A highly alpha-regioselective AgOTf-catalyzed nucleophilic substitution of the Baylis-Hillman acetates with indoles[J]. ORGANIC LETTERS,2007,9(13):2525-2528.
APA Shafiq, Zahid,Liu, Li,Liu, Zhe,Wang, Dong,&Chen, Yong-Jun.(2007).A highly alpha-regioselective AgOTf-catalyzed nucleophilic substitution of the Baylis-Hillman acetates with indoles.ORGANIC LETTERS,9(13),2525-2528.
MLA Shafiq, Zahid,et al."A highly alpha-regioselective AgOTf-catalyzed nucleophilic substitution of the Baylis-Hillman acetates with indoles".ORGANIC LETTERS 9.13(2007):2525-2528.

入库方式: OAI收割

来源:化学研究所

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