Yuehchukene analogs
E Wenkert, PDR Moeller, SR Piettre…
Index: Wenkert, Ernest; Moeller, Peter D. R.; Piettre, Serge R.; McPhail, Andrew T. Journal of Organic Chemistry, 1988 , vol. 53, # 14 p. 3170 - 3178
Full Text: HTML
Citation Number: 58
Abstract
Yuehchukene and the bisnoryuehchukenes have been synthesized by the dimerization of P- (dehydropreny1) indole and its demethyl derivative, respectively. Several routes of preparation of the monomers were developed. These 0-indolyl dienes were used in Diels- Alder reactions, the products of one of which served as intermediates in the synthesis of some seconoryuehchukenes.
Related Articles:
[Niu, Tianmin; Huang, Lehao; Wu, Tianxing; Zhang, Yuhong Organic and Biomolecular Chemistry, 2011 , vol. 9, # 1 p. 273 - 277]
[Pathak, Tejas P.; Osiak, Jaroslaw G.; Vaden, Rachel M.; Welm, Bryan E.; Sigman, Matthew S. Tetrahedron, 2012 , vol. 68, # 26 p. 5203 - 5208]
[Xu, Hai-Yan; Zi, You; Xu, Xiao-Ping; Wang, Shun-Yi; Ji, Shun-Jun Tetrahedron, 2013 , vol. 69, # 5 p. 1600 - 1605]
[Abe, Takumi; Nakamura, Shuuhei; Yanada, Reiko; Choshi, Tominari; Hibino, Satoshi; Ishikura, Minoru Organic Letters, 2013 , vol. 15, # 14 p. 3622 - 3625]
The reactions of nitrones with indoles
[Chalaye-Mauger, Helene; Denis, Jean-Noel; Averbuch-Pouchot, Marie-Therese; Vallee, Yannick Tetrahedron, 2000 , vol. 56, # 5 p. 791 - 804]