Henry reaction of fluorinated nitro compounds
H Hu, Y Huang, Y Guo
Index: Hu, Huawei; Huang, Yangen; Guo, Yong Journal of Fluorine Chemistry, 2012 , vol. 133, p. 108 - 114
Full Text: HTML
Citation Number: 8
Abstract
The Henry (nitroaldol) reaction of fluorinated nitro compounds with various aromatic aldehydes and a fluorinated aliphatic aldehyde to give β-fluoro-β-nitroalcohols which bearing a fluorinated quaternary carbon center was reported. The relative configuration of the major diastereoisomer of 2-fluoro-2-nitro-1-(4-nitrophenyl)-3-phenylpropanol (5bf) was determined by X-ray single crystal analysis.
Related Articles:
[McNulty, James; Nair, Jerald J.; Cheekoori, Sreedhar; Larichev, Vladimir; Capretta, Alfredo; Robertson Chemistry - A European Journal, 2006 , vol. 12, # 36 p. 9314 - 9322]
Easy and direct conversion of tosylates and mesylates into nitroalkanes
[Palmieri, Alessandr; Gabrielli, Serena; Ballini, Roberto Beilstein Journal of Organic Chemistry, 2013 , vol. 9, p. 533 - 536]
Easy and direct conversion of tosylates and mesylates into nitroalkanes
[Palmieri, Alessandr; Gabrielli, Serena; Ballini, Roberto Beilstein Journal of Organic Chemistry, 2013 , vol. 9, p. 533 - 536]
[Clark, James H.; Cork, David G.; Gibbs, Hugh W. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1983 , p. 2253 - 2258]
[Gorczynski, Michael J.; Smitherman, Pamela K.; Akiyama, Taro E.; Wood, Harold B.; Berger, Joel P.; King, S. Bruce; Morrow, Charles S. Journal of Medicinal Chemistry, 2009 , vol. 52, # 15 p. 4631 - 4639]