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The Peterson Reaction.

D. J. Ager, Synthesis, 1984, 384.

Key Words:
FUNCTIONAL GROUPS/PREPARATIONS/ALKENES/O=C-H/O=C-R/M-C-C-X/Si,OH/PETERSON/C=C/ALKENES/C=C-X/S/C=C-C=O/C=C-C=C/Si



The Peterson olefination reaction.

D. J. Ager, Org. React. (N.Y.), 1990, 38, 1.

Key Words:
ORGANOMETALLICS/SILICON/FUNCTIONAL GROUPS/PREPARATIONS/ALKENES/C-M(M')/Li(Si),Si(Sn)/C=C/Si



D. J. Ager, in Organometallics: Compounds of Group 15 (As, Sb, Bi) and Silicon Compounds, Vol. 4 (Ed.: I. Fleming), Georg Thieme Verlag, Stuttgart - New York, 2002, pp. 789.

Key Words:



Methodology to establish 1,2- and 1,3-difunctionality for the synthesis of carbohydrate derivatives.

D. J. Ager, M. B. East, Tetrahedron, 1992, 48, 2803.

Key Words:



The synthesis of carbohydrate derivatives from acyclic precursors.

D. J. Ager, M. B. East, Tetrahedron, 1993, 49, 5683.

Key Words:



D. J. Ager, M. B. East, CRC, Boca Raton, FL, 1996.

Key Words:



Reductions of 1,3-dicarbonyl systems with ruthenium-biarylbisphosphine catalysts.

D. J. Ager, S. A. Laneman, Tetrahedron: Asymmetry, 1997, 8, 3327.

Key Words:
DYNAMIC KINETIC RESOLUTION/CHIRAL DIPHOSPHINE-RUTHENIUM(II) CATALYSTS/STEREOSELECTIVE ASYMMETRIC HYDROGENATION/TRANSITION-METAL COMPLEXES/BETA-KETO-ESTERS/ENANTIOSELECTIVE SYNTHESIS/FUNCTIONALIZED KETONES/2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL BINAP/ALPHA-(ACYLAMINO)ACRYLIC ACIDS/DIPHOSPHINE LIGANDS



Commercial, synthetic nonnutritive sweeteners.

D. J. Ager, D. P. Pantaleone, S. A. Henderson, A. R. Katritzky, I. Prakash, D. E. Walters, Angew. Chem., Int. Ed. Engl., 1998, 37, 1803.

Key Words:
enzyme catalysis/sweeteners/synthetic methods/PSEUDOMONAS-AERUGINOSA ELASTASE/CATALYZED PEPTIDE-SYNTHESIS/HIGH-INTENSITY SWEETENER/AMINO-ACID DERIVATIVES/ASPARTAME PRECURSOR/IMMOBILIZED THERMOLYSIN/ORGANIC-SOLVENTS/METHYL-ESTER/ENZYMATIC-SYNTHESIS/TASTE



1,2-Amino alcohols and their heterocyclic derivatives as chiral auxiliaries in asymmetric synthesis.

D. J. Ager, I. Prakash, D. R. Schaad, Chem. Rev., 1996, 96, 835.

Key Words:
ALPHA-AMINO-ACIDS/HIGHLY ENANTIOSELECTIVE SYNTHESIS/GOLD(I)-CATALYZED ALDOL REACTION/LITHIUM ALUMINUM-HYDRIDE/TOXIC CYCLIC PEPTIDE/DIELS-ALDER REACTION/NUCLEOPHILIC AROMATIC-SUBSTITUTION/ASCIDIAN LISSOCLINUM-PATELLA/BETA-HYDROXY ACIDS/AZA-CLAISEN REARRANGEMENT



Chiral oxazolidinones in asymmetric synthesis.

D. J. Ager, I. Prakash, D. R. Schaad, Aldrichimica Acta, 1997, 30, 3.

Key Words:
ALPHA-AMINO-ACIDS/BETA-LACTAM ANTIBIOTICS/OPTICALLY PURE ISOMERS/HIV PROTEASE INHIBITORS/DIELS-ALDER REACTIONS/ALDOL REACTIONS/EFFICIENT METHOD/ENANTIOSELECTIVE SYNTHESIS/N-ACYLOXAZOLIDINONES/CONJUGATE ADDITION