Electron withdrawing substituents on equatorial and apical phosphines have opposite effects on the regioselectivity of rhodium catalyzed hydroformylation
…, EL Paulsen, EW Beuttenmueller, BR Proft…
文献索引:Casey, Charles P.; Lin Paulsen, Evelyn; Beuttenmueller, Eckart W.; Proft, Bernd R.; Petrovich, Lori M.; Matter, Brock A.; Powell, Douglas R. Journal of the American Chemical Society, 1997 , vol. 119, # 49 p. 11817 - 11825
The electronic effects of electron withdrawing aryl substituents on equatorial and apical diphosphines were investigated. Chelating diphosphines designed to coordinate in diequatorial or in apical-equatorial positions were synthesized, and their effects on the regioselectivity of rhodium catalyzed 1-hexene hydroformylation were observed. Only diequatorial coordination was observed for 2, 2'-bis [(diphenylphosphino) methyl]-1, 1'- ...
[Bricklebank, Neil; Godfrey, Stephen M.; McAuliffe, Charles A.; Deplano, Paula; Mercuri, Marie L.; Sheffield, Joanne M. Journal of the Chemical Society - Dalton Transactions, 1998 , # 14 p. 2379 - 2382]