中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Method to build 2,4-substituted selenazole from beta-azido diselenide and carboxylic acid: A formal synthesis of selenazofurin

文献类型:期刊论文

作者Du, Yuguo; Liu, Yi; Qiao, Junfei
刊名TETRAHEDRON
出版日期2018-06-14
卷号74期号:24页码:3061-3068
ISSN号0040-4020
文献子类Article
英文摘要A novel approach for the synthesis of 2,4-disubstituted selenazoles using carboxylic acids (or anhydrides) and beta-azido diselenide was achieved via a one-pot cascade formation of selenazoline (Staudinger reduction/diselenide cleavage/selenocarbonylation/aza-Wittig reaction) and a following MnO2-promoted oxidation. This method offers excellent substrate flexibility, and its valuable application is exemplified by an efficient total synthesis of Selenazofurin which exhibited good antitumor activities against K562 and A549 cells. (C) 2018 Elsevier Ltd. All rights reserved.
源URL[http://ir.rcees.ac.cn/handle/311016/40980]  
专题生态环境研究中心_环境化学与生态毒理学国家重点实验室
推荐引用方式
GB/T 7714
Du, Yuguo,Liu, Yi,Qiao, Junfei. Method to build 2,4-substituted selenazole from beta-azido diselenide and carboxylic acid: A formal synthesis of selenazofurin[J]. TETRAHEDRON,2018,74(24):3061-3068.
APA Du, Yuguo,Liu, Yi,&Qiao, Junfei.(2018).Method to build 2,4-substituted selenazole from beta-azido diselenide and carboxylic acid: A formal synthesis of selenazofurin.TETRAHEDRON,74(24),3061-3068.
MLA Du, Yuguo,et al."Method to build 2,4-substituted selenazole from beta-azido diselenide and carboxylic acid: A formal synthesis of selenazofurin".TETRAHEDRON 74.24(2018):3061-3068.

入库方式: OAI收割

来源:生态环境研究中心

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