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

  • WACKER–TSUJI Olefin Oxidation to WÜRTZ Coupling
    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 ‘W’. Reactions included in this section are: WACKER–TSUJI Olefin Oxidation; WAGNER–MEERWEIN Carbocation Rearrangement; WAKAMATSU (SYNGAS) Amino Acid Synthesis; WALLACH Azoxybenzene Rearrangement; WALLACH Imidazole Synthesis; WASSERMAN – BORMANN Macrocyclic Lactam Synthesis; WATANABE Heterocyclization; WEERMAN Carboxamide Degradation to Aldehydes; WEIDENHAGEN lmidazole Synthesis; WEINREB Ketone Synthesis; WEISS α-Dicarbornyl Annulation; WENCKER Aziridine Synthesis; WENDER Homologous Diels-Alder Reaction; WENZEL–IMAMOTO Selective Reduction; WESSELY–MOSER Dihydroxyxanthone Rearrangement; WESTPHAL Aza-bicycle Synthesis; WESTPHALEN–LETREE Carbocation Rearrangement; WHARTON Olefin Synthesis; WHITING Diene Synthesis; WIDEQUIST Cyanocyclopropane Synthesis; WILKES–ARMSTRONG Chiral Ionic Liquid Catalysts; WILKES–ROGERS Ionic Liquids; Wilkinson Decarbonylation Rh Catalyst; WILLGERODT–KINDLER Ketone to Amide Rearrangement; WILLIAMS – BEN ISHAI Amino Acid Synthesis; WILLIAMSON Ether Synthesis; WISSNER Hydroxyketone Synthesis; WITTIG Olefin Synthesis; WITTIG Allyl Ether Rearrangement; WOHL–AUE Phenazine Synthesis; WOHL–WEYGAND Aldose Degradation; WOHL – ZIEGLER Bromination; WOLFF α-Diazoketone Rearrangement; WOLFF – KISHNER C O Reduction; WOLFRAM – SCHORNIG – HANSDORF Carboxymethylation; WOODWARD Reagent for Peptide Synthesis; WURTZ Coupling

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

  • WACKER–TSUJI Olefin Oxidation to WÜRTZ Coupling
    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 ‘W’. Reactions included in this section are: WACKER–TSUJI Olefin Oxidation; WAGNER–MEERWEIN Carbocation Rearrangement; WAKAMATSU (SYNGAS) Amino Acid Synthesis; WALLACH Azoxybenzene Rearrangement; WALLACH Imidazole Synthesis; WASSERMAN – BORMANN Macrocyclic Lactam Synthesis; WATANABE Heterocyclization; WEERMAN Carboxamide Degradation to Aldehydes; WEIDENHAGEN lmidazole Synthesis; WEINREB Ketone Synthesis; WEISS α-Dicarbornyl Annulation; WENCKER Aziridine Synthesis; WENDER Homologous Diels-Alder Reaction; WENZEL–IMAMOTO Selective Reduction; WESSELY–MOSER Dihydroxyxanthone Rearrangement; WESTPHAL Aza-bicycle Synthesis; WESTPHALEN–LETREE Carbocation Rearrangement; WHARTON Olefin Synthesis; WHITING Diene Synthesis; WIDEQUIST Cyanocyclopropane Synthesis; WILKES–ARMSTRONG Chiral Ionic Liquid Catalysts; WILKES–ROGERS Ionic Liquids; Wilkinson Decarbonylation Rh Catalyst; WILLGERODT–KINDLER Ketone to Amide Rearrangement; WILLIAMS – BEN ISHAI Amino Acid Synthesis; WILLIAMSON Ether Synthesis; WISSNER Hydroxyketone Synthesis; WITTIG Olefin Synthesis; WITTIG Allyl Ether Rearrangement; WOHL–AUE Phenazine Synthesis; WOHL–WEYGAND Aldose Degradation; WOHL – ZIEGLER Bromination; WOLFF α-Diazoketone Rearrangement; WOLFF – KISHNER C O Reduction; WOLFRAM – SCHORNIG – HANSDORF Carboxymethylation; WOODWARD Reagent for Peptide Synthesis; WURTZ Coupling