Ruthenium??Catalyzed Regio??and Enantioselective Allylic Substitution with Water: Direct Synthesis of Chiral Allylic Alcohols
N Kanbayashi, K Onitsuka
Index: Kanbayashi, Naoya; Onitsuka, Kiyotaka Angewandte Chemie - International Edition, 2011 , vol. 50, # 22 p. 5197 - 5199
Full Text: HTML
Citation Number: 40
Abstract
Enantioselective allylic substitution catalyzed by transitionmetal complexes is an important process in organic synthesis.[1] For many years, mainly palladium complexes that contain chiral ligands have been employed as efficient catalysts in these reactions. Recent studies have demonstrated that chiral catalysts based on other transition metals show different regioselectivity in the synthesis of branched allylic products via monosubstituted π-allyl ...
Related Articles:
Natural feedstocks for diversity-oriented synthesis: macrolide-like scaffolds from nonactate
[Sumskaya, Yuliya G.; Swain, P. Whitney; Bergmeier, Stepehen C.; McMills, Mark C.; Priestley, Nigel D.; Wrighta, Dennis L. Arkivoc, 2011 , vol. 2011, # 5 p. 144 - 166]
[Dallanoce, Clelia; De Amici, Marco; Carrea, Giacomo; Secundo, Francesco; Castellano, Sabrina; De Micheli, Carlo Tetrahedron Asymmetry, 2000 , vol. 11, # 13 p. 2741 - 2751]
[Dallanoce, Clelia; De Amici, Marco; Carrea, Giacomo; Secundo, Francesco; Castellano, Sabrina; De Micheli, Carlo Tetrahedron Asymmetry, 2000 , vol. 11, # 13 p. 2741 - 2751]
Total Synthesis of (-)-Bulgecinine.
[Maeda, Mikiko; Okazaki, Fumiaki; Murayama, Mayumi; Tachibana, Yohko; Aoyagi, Yutaka; Ohta, Akihiro Chemical and Pharmaceutical Bulletin, 1997 , vol. 45, # 6 p. 962 - 965]
Total Synthesis of (-)-Bulgecinine.
[Maeda, Mikiko; Okazaki, Fumiaki; Murayama, Mayumi; Tachibana, Yohko; Aoyagi, Yutaka; Ohta, Akihiro Chemical and Pharmaceutical Bulletin, 1997 , vol. 45, # 6 p. 962 - 965]