中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Enantioselective Synthesis of Terminal 1,2-Diols from Acyl Chlorides

文献类型:期刊论文

作者Shao Panlin; Shen Litao; Ye Song
刊名CHINESE JOURNAL OF CHEMISTRY
出版日期2012-11-01
卷号30期号:11页码:2688-2692
关键词Acyl Chlorides Enantioselective Synthesis Cinchona Alkaloids Oxidation 1 2-diols
ISSN号1001-604X
DOI10.1002/cjoc.201200697
英文摘要Optically active terminal 1,2-diols were prepared with high enantiopurity via the TMS-quinidine-catalyzed enantioselective cyclization of acyl chlorides and oxaziridine, followed by reductive ring-opening of the cycloadducts.
语种英语
WOS记录号WOS:000311169300017
出版者WILEY-V C H VERLAG GMBH
源URL[http://ir.iccas.ac.cn/handle/121111/48157]  
专题中国科学院化学研究所
通讯作者Ye Song
作者单位Chinese Acad Sci, Inst Chem, CAS Key Lab Mol Recognit & Funct, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
推荐引用方式
GB/T 7714
Shao Panlin,Shen Litao,Ye Song. Enantioselective Synthesis of Terminal 1,2-Diols from Acyl Chlorides[J]. CHINESE JOURNAL OF CHEMISTRY,2012,30(11):2688-2692.
APA Shao Panlin,Shen Litao,&Ye Song.(2012).Enantioselective Synthesis of Terminal 1,2-Diols from Acyl Chlorides.CHINESE JOURNAL OF CHEMISTRY,30(11),2688-2692.
MLA Shao Panlin,et al."Enantioselective Synthesis of Terminal 1,2-Diols from Acyl Chlorides".CHINESE JOURNAL OF CHEMISTRY 30.11(2012):2688-2692.

入库方式: OAI收割

来源:化学研究所

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