中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation

文献类型:期刊论文

作者Xu LT(徐兰婷) ; Jiang YW(蒋咏文) ; Ma DW(马大为)
刊名Org. Lett.
出版日期2012
卷号14期号:4页码:1150-1153
ISSN号1523-7060
其他题名经由铜催化的芳基酰胺化合成3-取代和2,3-二取代喹唑啉酮
通讯作者马大为
英文摘要Cul/4-hydroxy-L-proline catalyzed coupling of N-substituted o-bromobenzamides with formamide takes place at 80 degrees C, affording 3-substituted quinazolinones directly. Under these conditions other amides that were tested only provided simple coupling products, which can be converted into 2,3-disubstituted quinazolinones via HMDS/ZnCl2 mediated condensative cyclization.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ol300084v
语种英语
WOS记录号WOS:000300339800050
公开日期2013-08-22
源URL[http://202.127.28.38/handle/331003/28025]  
专题上海有机化学研究所_金属有机化学国家重点实验室
推荐引用方式
GB/T 7714
Xu LT,Jiang YW,Ma DW. Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation[J]. Org. Lett.,2012,14(4):1150-1153.
APA 徐兰婷,蒋咏文,&马大为.(2012).Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation.Org. Lett.,14(4),1150-1153.
MLA 徐兰婷,et al."Synthesis of 3-Substituted and 2,3-Disubstituted Quinazolinones via Cu-Catalyzed Aryl Amidation".Org. Lett. 14.4(2012):1150-1153.

入库方式: OAI收割

来源:上海有机化学研究所

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