aquacobalamin and diazoacetic-ester

aquacobalamin has been researched along with diazoacetic-ester* in 1 studies

Other Studies

1 other study(ies) available for aquacobalamin and diazoacetic-ester

ArticleYear
Vitamin B12 derivatives as natural asymmetric catalysts: enantioselective cyclopropanation of alkenes.
    The Journal of organic chemistry, 2004, Apr-02, Volume: 69, Issue:7

    Vitamin B(12) derivatives were found for the first time to be general and efficient catalysts for asymmetric cyclopropanation of alkenes with ethyl diazoacetate (EDA). Among several common derivatives, aquocobalamin (B(12a)) was shown to be the most effective catalyst for a variety of alkenes, providing cis-dominant cyclopropanes in excellent yields and moderate enantioselectivity. Reactivity studies under different conditions suggest that the active species in the proposed catalytic cycle is the base-on cob(II)alamin (B(12r)) that is generated possibly via in situ reduction of B(12a) by EDA.

    Topics: Alkenes; Carboxylic Acids; Catalysis; Combinatorial Chemistry Techniques; Cyclopropanes; Diazonium Compounds; Indicators and Reagents; Molecular Structure; Stereoisomerism; Vitamin B 12

2004