Lewis acid mediated reactions of cyclopropyl aryl ketones with arylaldehydes, facile preparation of 2-(2-hydroxyethyl)-1,3-diarylpropenones
Shi M(施敏) ; Yang YH(杨永华) ; Xu B(胥波)
刊名Tetrahedron
2005
卷号61期号:7页码:1893-1901
其他题名Lewis酸催化的芳基环丙基酮和芳香醛的反应
通讯作者施敏
英文摘要In the presence of Lewis acid TMSOTf, ring-opening reaction of aryl cyclopropyl ketone with arylaldehyde took place under mild conditions to give 2-(2-hydroxyethyl)-1,3-diarylpropenone in good yield. By protection of hydroxy group with triethylsilyl group (TES), the corresponding ring-opened product 7 was obtained in high yield with good geometrical selectivity. (C) 2004 Elsevier Ltd. All rights reserved.
学科主题金属有机化学
收录类别SCI
原文出处http://dx.doi.org/10.1016/j.tet.2004.12.028
语种英语
WOS记录号WOS:000226915200028
公开日期2013-01-09
内容类型期刊论文
源URL[http://202.127.28.38/handle/331003/10026]  
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
Shi M,Yang YH,Xu B. Lewis acid mediated reactions of cyclopropyl aryl ketones with arylaldehydes, facile preparation of 2-(2-hydroxyethyl)-1,3-diarylpropenones[J]. Tetrahedron,2005,61(7):1893-1901.
APA Shi M,Yang YH,&Xu B.(2005).Lewis acid mediated reactions of cyclopropyl aryl ketones with arylaldehydes, facile preparation of 2-(2-hydroxyethyl)-1,3-diarylpropenones.Tetrahedron,61(7),1893-1901.
MLA Shi M,et al."Lewis acid mediated reactions of cyclopropyl aryl ketones with arylaldehydes, facile preparation of 2-(2-hydroxyethyl)-1,3-diarylpropenones".Tetrahedron 61.7(2005):1893-1901.
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