Chiral azabicyclo-N-oxyls mediated enantioselective electrooxidation of sec-alcohols
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چکیده
منابع مشابه
Catalytic asymmetric addition of alcohols to imines: enantioselective preparation of chiral N,O-aminals.
The enantioselective addition of alcohols to imine electrophiles has been shown to proceed in the presence of a catalytic amount of a chiral phosphoric acid catalyst. The reaction allows for the formation of the respective chiral N,O-aminals in excellent yield and enantioselectivity. A total of 11 different alcohols and 11 different imines were successfully used as a clear demonstration of the ...
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We demonstrate an efficient enantioselective oxidation of secondary alcohols catalyzed by Mn(III)-salen complex using N-bromosuccinimide (NBS) as the oxidant. The new protocol is very efficient for the oxidative kinetic resolution of a variety of secondary alcohols, including ortho-substituted benzylic alcohols.
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Enantioselective allylic substitution catalyzed by transitionmetal complexes is an important process in organic synthesis. For many years, mainly palladium complexes that contain chiral ligands have been employed as efficient catalysts in these reactions. Recent studies have demonstrated that chiral catalysts based on other transition metals show different regioselectivity in the synthesis of b...
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ژورنال
عنوان ژورنال: Tetrahedron Letters
سال: 2008
ISSN: 0040-4039
DOI: 10.1016/j.tetlet.2008.06.112