Ruzicka fukushima

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

  • ramberg backlund olefin synthesis to Ruzicka fukushima ketosteroid rearrangement
    Organic Syntheses Based on Name Reactions (Third Edition), 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 ‘R’. Reactions included in this section are: RAMBERG–BACKLUND Olefin Synthesis; RAPP–STOERMER Benzofuran Synthesis; RATHKE β-Keto Ester Synthesis; RAUHUT–CURRIER C O C C Condensation; REETZ Titanium Alkylation Reagent; REFORMATSKY Zinc Alkylation; REGITZ Diazo Transfer; REIMER–TIEMANN Phenol Formylation; REISSERT Cyanoamine Reaction; REISSERT Indole Synthesis; REMFRY–HULL Pyrimidine Synthesis; REPPE Acetylene Reactions; von RICHTER Aromatic Carboxylation; von RICHTER–WIDMAN–STOERMER Cinnoline Synthesis; RIECHE Formylation; RILEY Selenium Dioxide Oxidation; RITTER Amidation; ROBINSON Cycloalkanone Annulation; ROBINSON–ALLAN–KOSTANECKI Chromone Synthesis; ROBINSON–FOULDS Quinoline Synthesis; ROBINSON – GABRIEL Oxazole Synthesis; ROELEN Olefin Carbonylation; ROSENMUND Aromatic Halide Arsonylation; ROSENMUND Acyl Chloride to Aldehyde Reduction; ROSENMUND–BRAUN Aromatic Cyanation; ROSINI–BARTOLI Reductive Nitroarene Alkylation; ROSKAMP β-Ketoester Synthesis; ROTHENMUND–LINDSEY Porphine Synthesis; ROVIS–ENDERS Asymmetric Stetter Reaction via Carbenes; ROZEN Hypofluorite Reagents; RUFF–FENTON Aldose Degradation; RUPE Propargyl Alcohol Rearrangement; RUPPERT Perfluoroalkylation; RUSSIG – LAATSCH Hydroquinone Monoether Formation; Ruzickafukushima Ketosteroid Rearrangement

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

  • ramberg backlund olefin synthesis to Ruzicka fukushima ketosteroid rearrangement
    Organic Syntheses Based on Name Reactions (Third Edition), 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 ‘R’. Reactions included in this section are: RAMBERG–BACKLUND Olefin Synthesis; RAPP–STOERMER Benzofuran Synthesis; RATHKE β-Keto Ester Synthesis; RAUHUT–CURRIER C O C C Condensation; REETZ Titanium Alkylation Reagent; REFORMATSKY Zinc Alkylation; REGITZ Diazo Transfer; REIMER–TIEMANN Phenol Formylation; REISSERT Cyanoamine Reaction; REISSERT Indole Synthesis; REMFRY–HULL Pyrimidine Synthesis; REPPE Acetylene Reactions; von RICHTER Aromatic Carboxylation; von RICHTER–WIDMAN–STOERMER Cinnoline Synthesis; RIECHE Formylation; RILEY Selenium Dioxide Oxidation; RITTER Amidation; ROBINSON Cycloalkanone Annulation; ROBINSON–ALLAN–KOSTANECKI Chromone Synthesis; ROBINSON–FOULDS Quinoline Synthesis; ROBINSON – GABRIEL Oxazole Synthesis; ROELEN Olefin Carbonylation; ROSENMUND Aromatic Halide Arsonylation; ROSENMUND Acyl Chloride to Aldehyde Reduction; ROSENMUND–BRAUN Aromatic Cyanation; ROSINI–BARTOLI Reductive Nitroarene Alkylation; ROSKAMP β-Ketoester Synthesis; ROTHENMUND–LINDSEY Porphine Synthesis; ROVIS–ENDERS Asymmetric Stetter Reaction via Carbenes; ROZEN Hypofluorite Reagents; RUFF–FENTON Aldose Degradation; RUPE Propargyl Alcohol Rearrangement; RUPPERT Perfluoroalkylation; RUSSIG – LAATSCH Hydroquinone Monoether Formation; Ruzickafukushima Ketosteroid Rearrangement