Efficient Aldolase Catalytic Antibodies That Use the Enamine Mechanism of Natural Enzymes
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R. Lerner | C. Barbas | C F Barbas | R A Lerner | J Wagner | J. Wagner
[1] Chi‐Huey Wong,et al. SEQUENTIAL ONE-POT ALDOL REACTIONS CATALYZED BY 2-DEOXYRIBOSE-5-PHOSPHATE ALDOLASE AND FRUCTOSE-1,6-DIPHOSPHATE ALDOLASE , 1995 .
[2] Isamu Shiina,et al. Catalytic asymmetric aldol-type reaction using a chiral tin(II) Lewis acid , 1993 .
[3] A. Kato,et al. Kinetic studies of fast equilibrium by means of high-performance liquid chromatography. Part 11. Keto–enol tautomerism of some β-dicarbonyl compounds , 1986 .
[4] R. Lerner,et al. Control of the exo and endo pathways of the Diels-Alder reaction by antibody catalysis. , 1993, Science.
[5] R. Lerner,et al. CROSSING EXTREME MECHANISTIC BARRIERS BY ANTIBODY CATALYSIS : SYN ELIMINATION TO A CIS OLEFIN , 1994 .
[6] W. Rutter,et al. EVOLUTION OF ALDOLASE. , 1964, Federation proceedings.
[7] E. Carreira,et al. Catalytic, Enantioselective Acetone Aldol Additions with 2-Methoxypropene , 1995 .
[8] P G Schultz,et al. At the crossroads of chemistry and immunology: catalytic antibodies. , 1991, Science.
[9] C. Milstein,et al. Continuous cultures of fused cells secreting antibody of predefined specificity , 1975, Nature.
[10] I. Paterson. New methods and strategies for the stereocontrolled synthesis of polypropionate-derived natural products , 1992 .
[11] D. Evans. Stereoselective organic reactions: catalysts for carbonyl addition processes. , 1988, Science.
[12] Chi-Huey Wong,et al. Deoxyribose-5-phosphate aldolase as a synthetic catalyst , 1990 .
[13] C. Barbas,et al. Assembly of combinatorial antibody libraries on phage surfaces: the gene III site. , 1991, Proceedings of the National Academy of Sciences of the United States of America.
[14] Chi‐Huey Wong,et al. Deoxyribose 5-phosphate aldolase as a catalyst in asymmetric aldol condensation , 1992 .
[15] C. Barbas,et al. Direct selection for a catalytic mechanism from combinatorial antibody libraries. , 1994, Proceedings of the National Academy of Sciences of the United States of America.
[16] C. Lai,et al. Amino Acid Sequence of Rabbit Muscle Aldolase and the Structure of the Active Center , 1974, Science.
[17] F. Westheimer,et al. Acetoacetate decarboxylase. Reaction with acetopyruvate. , 1968, Biochemistry.
[18] T. Bach. Catalytic Enantioselective CC Coupling—Allyl Transfer and Mukaiyama Aldol Reaction , 1994 .
[19] J. Reymond,et al. Catalytic, enantioselective aldol reaction using antibodies against a quaternary ammonium ion with a primary amine cofactor , 1995 .
[20] Clayton H. Heathcock,et al. Acyclic stereoselection. 40. Steric effects, as well as .sigma.*-orbital energies, are important in diastereoface differentiation in additions to chiral aldehydes , 1987 .
[21] Chi‐Huey Wong,et al. Recombinant 2-Deoxyribose-5-phosphate Aldolase in Organic Synthesis: Use of Sequential Two-Substrate and Three-Substrate Aldol Reactions , 1995 .
[22] K. Furuta,et al. CATALYTIC ASYMMETRIC ALDOL REACTIONS. USE OF A CHIRAL (ACYLOXY)BORANE COMPLEX AS A VERSATILE LEWIS ACID CATALYST , 1991 .
[23] D. Cram,et al. Studies in Stereochemistry. X. The Rule of “Steric Control of Asymmetric Induction” in the Syntheses of Acyclic Systems , 1952 .
[24] C H Heathcock,et al. Acyclic Stereocontrol Through the Aldol Condensation , 1981, Science.
[25] A. J. Morris,et al. Lysine-146 of rabbit muscle aldolase is essential for cleavage and condensation of the C3-C4 bond of fructose 1,6-bis(phosphate). , 1994, Biochemistry.
[26] Clayton H. Heathcock,et al. Acyclic stereoselection. 16. High diastereofacial selectivity in Lewis acid mediated additions of enol silanes to chiral aldehydes , 1983 .
[27] J. Petersen,et al. Double Asymmetric Synthesis and a New Strategy for Stereochemical Control in Organic Synthesis , 1985 .
[28] W. Jencks,et al. Entropic contributions to rate accelerations in enzymic and intramolecular reactions and the chelate effect. , 1971, Proceedings of the National Academy of Sciences of the United States of America.
[29] H. Zimmerman,et al. The Stereochemistry of the Ivanov and Reformatsky Reactions. I , 1957 .