A Ring??Closing Metathesis Pathway to Fluorovinyl??Containing Nitrogen Heterocyles
V De Matteis, FL van Delft, J Tiebes…
Index: De Matteis, Valeria; Van Delft, Floris L.; Tiebes, Joerg; Rutjes, Floris P. J. T. European Journal of Organic Chemistry, 2006 , # 5 p. 1166 - 1176
Full Text: HTML
Citation Number: 17
Abstract
Abstract The synthesis of highly functionalized fluorinated piperidines is described. The key step in this synthesis is a ring-closing metathesis reaction involving fluoride-substituted olefins, which leads to the corresponding cyclic vinyl fluorides. Several sequences to arrive at differently substituted piperidines have been evaluated.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2006)
Related Articles:
[Del Valle, David J.; Krische, Michael J. Journal of the American Chemical Society, 2013 , vol. 135, # 30 p. 10986 - 10989]
[Choudary, Boyapati M.; Chowdari, Naidu S.; Kantam, Mannepalli L. Tetrahedron, 2000 , vol. 56, # 37 p. 7291 - 7298]
[Dong, Xiang; Sang, Rui; Wang, Qiang; Tang, Xiang-Ying; Shi, Min Chemistry - A European Journal, 2013 , vol. 19, # 50 p. 16910 - 16915]
[Koizumi, Toshio; Fuchigami, Toshio; Nonaka, Tsutomu Bulletin of the Chemical Society of Japan, 1989 , vol. 62, # 1 p. 219 - 225]