Davidson Oxazole Synthesis

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I. Namboothiri - One of the best experts on this subject based on the ideXlab platform.

  • DAKIN Phenol Oxidation to DUTT–WORMALL Azide Synthesis
    Organic Syntheses Based on Name Reactions, 2012
    Co-Authors: Alfred Hassner, I. Namboothiri
    Abstract:

    This article contains brief overviews, mechanisms and practical details for organic Synthesis named reactions and processes beginning with the letter ‘D’. Reactions included in this section are: DAKIN Phenol Oxidation; DAKIN–WEST Ketone Synthesis; DANHEISER Silylallene Annulation; DANISHEFSKY Dienes; DARAPSKI Amino Acid Synthesis; DARZENS Epoxide Synthesis; DARZENS–NENITZESCU C C Acylation; Davidson Oxazole Synthesis; DAVID–THIEFFRY Monophenylation of Diols; DAVIES Fe Chiral Auxiliary; DAVIS–ELLMAN Chiral Sulfinimines; DAVIS Oxaziridine Oxidizing Reagent; DE KIMPE Aziridine, Amidine Synthesis; DE MAYO C C Photocycloaddition; DELEPINE Aldehyde Oxidation; DELEPINE Amine Synthesis; DEMJANOV Diazonium Rearrangement; DESS–MARTIN Alcohol Oxidizing Reagent; DIECKMANN Diester Cyclization; DIELS–ALDER Cyclohexene Synthesis; DIELS–ALDER ASYMMETRIC Reaction; DIMROTH R-N Rearrangement; DIMROTH Triazole Synthesis; DJERASSI–RYLANDER RuO 4 Oxidating Agent; DOEBNER–MILLER Quinoline Synthesis; DOERING Alcohol Oxidation; DOERING–La FLAMME Allene Synthesis; DONDONI C O Homologation; DOTZ Hydroquinone Synthesis; DOWD Cyclic Ketone Ring Expansion; DUFF Aromatic Aldehyde Synthesis; DUTHALER–HAFNER Enantioselective Allylation; DUTT–WORMALL Azide Synthesis

Alfred Hassner - One of the best experts on this subject based on the ideXlab platform.

  • DAKIN Phenol Oxidation to DUTT–WORMALL Azide Synthesis
    Organic Syntheses Based on Name Reactions, 2012
    Co-Authors: Alfred Hassner, I. Namboothiri
    Abstract:

    This article contains brief overviews, mechanisms and practical details for organic Synthesis named reactions and processes beginning with the letter ‘D’. Reactions included in this section are: DAKIN Phenol Oxidation; DAKIN–WEST Ketone Synthesis; DANHEISER Silylallene Annulation; DANISHEFSKY Dienes; DARAPSKI Amino Acid Synthesis; DARZENS Epoxide Synthesis; DARZENS–NENITZESCU C C Acylation; Davidson Oxazole Synthesis; DAVID–THIEFFRY Monophenylation of Diols; DAVIES Fe Chiral Auxiliary; DAVIS–ELLMAN Chiral Sulfinimines; DAVIS Oxaziridine Oxidizing Reagent; DE KIMPE Aziridine, Amidine Synthesis; DE MAYO C C Photocycloaddition; DELEPINE Aldehyde Oxidation; DELEPINE Amine Synthesis; DEMJANOV Diazonium Rearrangement; DESS–MARTIN Alcohol Oxidizing Reagent; DIECKMANN Diester Cyclization; DIELS–ALDER Cyclohexene Synthesis; DIELS–ALDER ASYMMETRIC Reaction; DIMROTH R-N Rearrangement; DIMROTH Triazole Synthesis; DJERASSI–RYLANDER RuO 4 Oxidating Agent; DOEBNER–MILLER Quinoline Synthesis; DOERING Alcohol Oxidation; DOERING–La FLAMME Allene Synthesis; DONDONI C O Homologation; DOTZ Hydroquinone Synthesis; DOWD Cyclic Ketone Ring Expansion; DUFF Aromatic Aldehyde Synthesis; DUTHALER–HAFNER Enantioselective Allylation; DUTT–WORMALL Azide Synthesis

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