An efficient synthesis of benzofurans and their application in the preparation of natural products of the genus Calea
M del Carmen Cruz, J Tamariz
Index: Del Carmen Cruz, Maria; Tamariz, Joaquin Tetrahedron, 2005 , vol. 61, # 42 p. 10061 - 10072
Full Text: HTML
Citation Number: 29
Abstract
The intramolecular cyclization of the β-substituted olefins methyl 2-aryloxy-3- dimethylaminopropenoates catalyzed by Lewis acids leads to a short and novel synthesis of benzofurans. When the olefins 4-dimethylamino-3-aryloxy-3-buten-2-ones were used, the cyclization process was faster and provided the corresponding substituted 2- acetylbenzofurans. Among the latter, naturally occurring compounds calebertin (), ...
Related Articles:
[Shi, Guo Q.; Dropinski, James F.; Zhang, Yong; Santini, Conrad; Sahoo, Soumya P.; Berger, Joel P.; MacNaul, Karen L.; Zhou, Gaochao; Agrawal, Arun; Alvaro, Raul; Cai, Tian-Quan; Hernandez, Melba; Wright, Samuel D.; Moller, David E.; Heck, James V.; Meinke, Peter T. Journal of Medicinal Chemistry, 2005 , vol. 48, # 17 p. 5589 - 5599]
[Cruz, Maria Del Carmen; Tamariz, Joaquin Tetrahedron Letters, 2004 , vol. 45, # 11 p. 2377 - 2380]