Recent Development in Asymmetric Oxidation of Olefinic Double bond
نویسندگان
چکیده
منابع مشابه
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Abstract. The Ti(OiPr)4/tartaric acid diethyl ester/t-BuOOH complex (Sharpless catalyst) was successfully used for the direct asymmetric oxidation of ketones resulting in lactones from cyclobutanones; α,β-dihydroxy ketones from β-hydroxy ketones; alkyl lactone carboxylic acids from 3-alkylcyclopentane-1,2-diones; and spiro-γ-dilactone from 3-(2-hydroxyethyl)cyclopentane1,2-dione in high enantio...
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A copper(I)-catalyzed, (diacetoxyiodo)benzene [PhI(OAc)2]-mediated ring-expansion/thiolactonization of a-oxo ketene dithioacetals was efficiently realized via azidation of the internal olefinic C@H bond with sodium azide under mild conditions. Sequential amination, ring-expansion rearrangement, and thiolactonization occurred to form aminated thiolactones in the presence of acetic anhydride as t...
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ژورنال
عنوان ژورنال: Journal of Japan Oil Chemists' Society
سال: 1990
ISSN: 1884-2003
DOI: 10.5650/jos1956.39.10_858