A rapid synthesis of 2-aryl-5-substituted-2,3-dihydrobenzofurans

被引:39
作者
Kuethe, JT [1 ]
Wong, A [1 ]
Journet, M [1 ]
Davies, IW [1 ]
机构
[1] Merck & Co Inc, Dept Proc Res, Rahway, NJ 07065 USA
关键词
D O I
10.1021/jo0500941
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
An effective strategy has been developed for the rapid and efficient one-pot synthesis of 2-aryl-5-substituted-2,3-dihydrobenzofurans from readily available o-nitrotoluenes and aromatic aldehydes. This strategy allows access to a structurally diverse array of products for further manipulation.
引用
收藏
页码:3727 / 3729
页数:3
相关论文
共 63 条
[61]   A convenient ring formation of 3-aryl-2,2-dialkyl-2,3-dihydrobenzofurans from phenols and 2-aryl-2,2-dialkylacetaldehydes [J].
Yamashita, M ;
Ono, Y ;
Tawada, H .
TETRAHEDRON, 2004, 60 (12) :2843-2849
[62]   SYNTHETIC STUDIES ON FR900482 - PROMISING METHOD TO CONSTRUCT THE BICYCLIC HYDROXYLAMINE HEMI-KETAL RING-SYSTEM [J].
YASUDA, N ;
WILLIAMS, RM .
TETRAHEDRON LETTERS, 1989, 30 (26) :3397-3400
[63]   First synthesis of naturally occurring (±)-epi-conocarpan [J].
Zheng, SL ;
Yu, WY ;
Xu, MX ;
Che, CM .
TETRAHEDRON LETTERS, 2003, 44 (07) :1445-1447