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Burk, Mark J., Harper, T. Gregory P., Kalberg, Christopher S. (1995) Highly Enantioselective Hydrogenation of .beta.-Keto Esters under Mild Conditions. Journal Of The American Chemical Society, 117 (15) 4423-4424 doi:10.1021/ja00120a035

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Reference TypeJournal (article/letter/editorial)
TitleHighly Enantioselective Hydrogenation of .beta.-Keto Esters under Mild Conditions
JournalJournal Of The American Chemical Society
AuthorsBurk, Mark J.Author
Harper, T. Gregory P.Author
Kalberg, Christopher S.Author
Year1995 (April)Volume117
Issue15
PublisherAmerican Chemical Society (ACS)
DOIdoi:10.1021/ja00120a035Search in ResearchGate
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Mindat Ref. ID1489617Long-form Identifiermindat:1:5:1489617:0
GUID0
Full ReferenceBurk, Mark J., Harper, T. Gregory P., Kalberg, Christopher S. (1995) Highly Enantioselective Hydrogenation of .beta.-Keto Esters under Mild Conditions. Journal Of The American Chemical Society, 117 (15) 4423-4424 doi:10.1021/ja00120a035
Plain TextBurk, Mark J., Harper, T. Gregory P., Kalberg, Christopher S. (1995) Highly Enantioselective Hydrogenation of .beta.-Keto Esters under Mild Conditions. Journal Of The American Chemical Society, 117 (15) 4423-4424 doi:10.1021/ja00120a035
In(1995, April) Journal Of The American Chemical Society Vol. 117 (15) American Chemical Society (ACS)

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Burk, Mark J., Kalberg, Christopher S., Pizzano, Antonio (1998) Rh−DuPHOS-Catalyzed Enantioselective Hydrogenation of Enol Esters. Application to the Synthesis of Highly Enantioenriched α-Hydroxy Esters and 1,2-Diols. Journal Of The American Chemical Society, 120 (18) 4345-4353 doi:10.1021/ja974278b
Burk, Mark J., Gross, Michael F., Martinez, Jose P. (1995) Asymmetric catalytic synthesis of .beta.-branched amino acids via highly enantioselective hydrogenation of .alpha.-enamides. Journal Of The American Chemical Society, 117 (36) 9375-9376 doi:10.1021/ja00141a039
LeBlond, C., Wang, J., Liu, J., Andrews, A. T., Sun, Y.-K. (1999) Highly Enantioselective Heterogeneously Catalyzed Hydrogenation of α-Ketoesters under Mild Conditions. Journal Of The American Chemical Society, 121 (20) 4920-4921 doi:10.1021/ja990653j
Burk, Mark J. (1991) C2-symmetric bis(phospholanes) and their use in highly enantioselective hydrogenation reactions. Journal Of The American Chemical Society, 113 (22) 8518-8519 doi:10.1021/ja00022a047
Burk, Mark J., Feaster, John E. (1992) Enantioselective hydrogenation of the C:N group: a catalytic asymmetric reductive amination procedure. Journal Of The American Chemical Society, 114 (15) 6266-6267 doi:10.1021/ja00041a067
Burk, Mark J., Feng, Shaoguang, Gross, Michael F., Tumas, William (1995) Asymmetric catalytic hydrogenation reactions in supercritical carbon dioxide. Journal Of The American Chemical Society, 117 (31) 8277-8278 doi:10.1021/ja00136a029
Kitamura, M., Tokunaga, M., Noyori, R. (1995) Asymmetric Hydrogenation of .beta.-Keto Phosphonates: A Practical Way to Fosfomycin. Journal Of The American Chemical Society, 117 (10) 2931-2932 doi:10.1021/ja00115a030
Burk, Mark J., Pizzano, Antonio, Martín, José A., Liable-Sands, Louise M., Rheingold, Arnold L. (2000) Bis(phospholane) Ligands Containing Chiral Backbones. Matching and Mismatching Effects in Enantioselective Hydrogenation of α-Keto Esters. Organometallics, 19. 250-260 doi:10.1021/om990730j
Burk, Mark J., Allen, John G., Kiesman, William F. (1998) Highly Regio- and Enantioselective Catalytic Hydrogenation of Enamides in Conjugated Diene Systems:  Synthesis and Application of γ,δ-Unsaturated Amino Acids. Journal Of The American Chemical Society, 120 (4) 657-663 doi:10.1021/ja9731074
Burk, Mark J., Feaster, John E., Nugent, William A., Harlow, Richard L. (1993) Preparation and use of C2-symmetric bis(phospholanes): production of .alpha.-amino acid derivatives via highly enantioselective hydrogenation reactions. Journal Of The American Chemical Society, 115 (22) 10125-10138 doi:10.1021/ja00075a031
Burk, Mark J., Wang, Yan Ming, Lee, Jeffrey R. (1996) A Convenient Asymmetric Synthesis of α-1-Arylalkylamines through the Enantioselective Hydrogenation of Enamides. Journal Of The American Chemical Society, 118 (21) 5142-5143 doi:10.1021/ja953872n
 
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