C2-symmetric bis (phospholanes) and their use in highly enantioselective hydrogenation reactions
MJ Burk
Index: Burk, Mark J. Journal of the American Chemical Society, 1991 , vol. 113, # 22 p. 8518 - 8519
Full Text: HTML
Citation Number: 523
Abstract
Asymmetric catalysis is one of the most powerful, economically feasible methods for the generation of enantiomerically enriched compounds. C2-Symmetric chiral diphosphines have emerged as a valuable class of ligands in transition-metal-based asymmetric catalysis, and in certain cases, spectacular enantioselectivity has been observed.'We recently reported the preparation and use of a variety of new electron-rich chiral phospholane ...
Related Articles:
Catalytic asymmetric hydrogenation of methyl (E)-and (Z)-2-acetamido-3-alkylacrylates
[Journal of Organic Chemistry, , vol. 46, p. 5086 - 5093]
Total synthesis of the serine-threonine phosphatase inhibitor microcystin-LA
[Garcia, Jordi; Gonzalez, Javier; Segura, Ramon; Vilarrasa, Jaume Tetrahedron, 1984 , vol. 40, # 16 p. 3121 - 3128]
Catalytic asymmetric hydrogenation of methyl (E)-and (Z)-2-acetamido-3-alkylacrylates
[Journal of Organic Chemistry, , vol. 46, p. 5086 - 5093]
Deprotection of N??Nosyl?螃窿?amino Acids by Using Solid??Supported Mercaptoacetic Acid
[De Marco, Rosaria; Gioia, Maria Luisa Di; Leggio, Antonella; Liguori, Angelo; Viscomi, Maria Caterina European Journal of Organic Chemistry, 2009 , # 22 p. 3795 - 3800]
Oxidation of peptides by methyl (trifluoromethyl) dioxirane: the protecting group matters
[Rella, Maria Rosaria; Williard, Paul G. Journal of Organic Chemistry, 2007 , vol. 72, # 2 p. 525 - 531]