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    Chiral base-mediated rearrangement of meso-cyclohexene oxides to allylic alcohols
    Tetrahedron Letters (1996)
    Peter O’BrienPierre Poumellec
    29
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    Keywords:
    Lithium amide
    Cyclohexenone
    Diastereomer
    Allylic alcohol
    Cyclohexene oxide
    Amide
    Base (topology)
    Topics:
    Asymmetric Synthesis and Catalysis
    Synthetic Organic Chemistry Methods
    Advanced Synthetic Organic Chemistry
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    Diastereomer
    Lithium amide
    Cyclohexene oxide
    Cyclohexanes
    Amide
    Allylic alcohol
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    Chiral base-mediated rearrangement of meso-cyclohexene oxides to allylic alcohols
    Tetrahedron Letters (1996)
    Peter O’BrienPierre Poumellec
    Lithium amide
    Cyclohexenone
    Diastereomer
    Allylic alcohol
    Cyclohexene oxide
    Amide
    Base (topology)
    Citations (29)
    Complexes of hybrid copolymers with heavy metals: preparation, properties and application as catalysts for oxidation
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    Synthesis, characterization and catalytic oxyfunctionalization of cyclohexene with tert-butylhydroperoxide and hydrogen peroxide in the presence of alumina-supported Mn(II), Co(II), Ni(II) and Cu(II) bis(2-hydroxyanil)benzil complexes
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    Masoud Salavati‐NiasariSeyed M. Mirsattari
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    ChemInform Abstract: Epoxidation of Olefins Using a CrO3/TBHP System.
    ChemInform (1990)
    D. D. AgarwalShubhi SrivastavaPoonam Chadha
    Abstract The epoxidation of cyclohexene using CrO3/tert.‐butylhydroperoxide gives cyclohexene oxide, cyclohexenol and cyclohexenone in the ratio 3:1:40.
    Cyclohexene oxide
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    Synthesis, Characterization, and Activity in the Epoxidation of Cyclohexene with Aqueous H2O2of Catalysts Prepared by Reaction of TiF4with Silica
    Journal of Catalysis (1998)
    Elisabet Fuguet i JordàA. TuelR. TeissierJ. Kervennal
    Cyclohexene oxide
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    Continuous Synthesis of Cyclohexene Oxide in a Micro‐FlowSystem
    ChemistrySelect (2018)
    Yu ZhouWei HeZheng FangKai Guo
    Abstract Epoxidation reaction catalyzed by dicyclohexylcarbodiimide(DCC) was realized in a microflow system, resulting in cyclohexene oxide with high yields. In this study, the epoxidation process of cyclohexene in MFS was investigated in detail. The optimal yield was obtained in such conditions: temperature 80°C, residence time 12 min, catalyst concentration 3%, ratio of cyclohexene to UHP 1:8. Basic additions played an important role in the collapse of adducts.
    Cyclohexene oxide
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