Enantioselective preparation of α-acyloxy ketones from α-hydroxy and α-amino acids

References

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	Year	Citations
L-Lactate dehydrogenase: substrate specificity and use as a catalyst in the synthesis of homochiral 2-hydroxy acids Mahn Joo Kim, George M. Whitesides Journal of the American Chemical Society Bioorganic ChemistryEngineeringAltmetric Attention ScoreSecondary MetaboliteEnzymatic Modification	1988	149
Chemistry of oxaziridines. 14. Asymmetric oxidation of ketone enolates using enantiomerically pure (camphorylsulfonyl)oxaziridine Franklin A. Davis, Aurelia C. Sheppard, Bang Chi Chen, Journal of the American Chemical Society Bioorganic ChemistryKetone EnolatesNatural SciencesAsymmetric OxidationAltmetric Attention Score	1990	148
Protocols for the preparation of each of the four possible stereoisomeric .alpha.-alkyl-.beta.-hydroxy carboxylic acids from a single chiral aldol reagent Nanine A. Van Draanen, Siméon Arseniyadis, Michael T. Crimmins, The Journal of Organic Chemistry EngineeringBiochemistryDonut IconNatural SciencesDiversity-oriented Synthesis	1991	146
Studies on Diastereoisomeric α-Amino Acids and Corresponding α-Hydroxy Acids. VII. Influence of β-Configuration on Enzymic Susceptibility Milton Winitz, Leah Bloch-Frankenthal, Nobuo Izumiya, Journal of the American Chemical Society Pharmaceutical ScienceBioorganic ChemistryAltmetric Attention ScoreChemical BiologyEnzymatic Modification	1956	132
Configuration of Carbohydrates, Hydroxy-Acids and Amino-Acids: Configurations of Amino-Compounds and the Steric Course of Deamination PHYLLIS BREWSTER, FRANK HIRON, E. D. Hughes, Nature Steric CourseEngineeringBiochemistryGlycobiologyOrganic Chemistry	1950	116
A very mild, catalytic and versatile procedure for α-oxidation of ketone silyl enol ethers using (salen)manganese(<scp>III</scp>) complexes; a new, chiral complex giving asymmetric induction. A possible model for selective biochemical oxidative reactions through enol formation D. Reddeppa Reddy, Edward R. Thornton Journal of the Chemical Society Chemical Communications Inorganic ChemistryChemical EngineeringTerminal OxidantEngineeringBiochemistry	1992	71
Organomanganese (II) reagents XIX. Acylation of organomanganese chlorides by carboxylic acid chlorides in THF: A clear improvement in the field of the preparation of ketones from organomanganese compounds Gérard Cahiez, Blandine Laboue Tetrahedron Letters Organomanganese ChloridesEngineeringOrganomanganese CompoundsOrganic ChemistryStereoselective Synthesis	1989	63
Organomanganese (II) reagents XXIII: Manganese-catalyzed acylation of organomagnesium compounds by car☐ylic acid chlorides Ge ́rard Cahiez, Blandine Laboue Tetrahedron Letters Organomagnesium CompoundsInorganic ChemistryChemical EngineeringEngineeringManganese-catalyzed Acylation	1992	60
Preparation, reactivity, and spectral properties of 1,3-dioxin vinylogous esters: versatile .beta.-ketovinyl cation equivalents Amos B. Smith, Bruce D. Dorsey, Masashi Ohba, The Journal of Organic Chemistry Enantioselective SynthesisEngineeringChemical AnalysisDonut IconSpectral Properties	1988	58
Remarkable optical induction in the reduction of .alpha.-oxo esters with B-(3-pinanyl)-9-borabicyclo[3.3.1]nonane. Synthesis of .alpha.-hydroxy esters of 100% optical purity Herbert C. Brown, Ganesh G. Pai, Prabhakar K. Jadhav Journal of the American Chemical Society Chemical EngineeringOptical MaterialsEngineering.Alpha.-hydroxy EstersPhotochemistry	1984	56

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