Phosphine–olefin ligands: a facile dehydrogenative route to catalytically active rhodium complexes
TM Douglas, J Le Nôtre, SK Brayshaw…
Index: Douglas, Thomas M.; Notre, Jerome Le; Brayshaw, Simon K.; Frost, Christopher G.; Weller, Andrew S. Chemical Communications, 2006 , # 32 p. 3408 - 3410
Full Text: HTML
Citation Number: 0
Abstract
The synthesis of mixed phosphine–olefin ligands is of significant interest. 4–7 Such ligands have been used by Hayashi et al. (CScheme 1) in the catalysis of 1,4-addition reactions 6 and by Grützmacher in hydrogenation reactions. 7 However, the synthesis of such ligands is multistep and can be non-trivial. Here we report the straightforward and facile synthesis of a rhodium complex containing a phosphine–olefin ligand (D) by the dehydrogenation of a cyclopentyl group in the ...
Related Articles:
[Tang, Yi-Qiang; Lv, Huan; He, Xiao-Na; Lu, Jian-Mei; Shao, Li-Xiong Catalysis Letters, 2011 , vol. 141, # 5 p. 705 - 708]
[Zhou, Yang; Li, Xinyao; Hou, Shili; Xu, Jiaxi Journal of Molecular Catalysis A: Chemical, 2012 , vol. 365, p. 203 - 211]
Alcohols as electrophiles: iron-catalyzed Ritter reaction and alcohol addition to alkynes
[Jefferies, Latisha R.; Cook, Silas P. Tetrahedron, 2014 , vol. 70, # 27-28 p. 4204 - 4207]
[Yamamoto, Tetsuya; Iizuka, Michiko; Takenaka, Hiroto; Ohta, Tetsuo; Ito, Yoshihiko Journal of Organometallic Chemistry, 2009 , vol. 694, # 9-10 p. 1325 - 1332]
[Cho, Chan Sik; Motofusa, Shin-ichi; Ohe, Kouichi; Uemura, Sakae; Shim, Sang Chul Journal of Organic Chemistry, 1995 , vol. 60, # 4 p. 883 - 888]