1,2,3-Triols: Partial Oxidation of γ-Silyl Allylic Alcohols with Ozone
نویسندگان
چکیده
منابع مشابه
Radical 1,2-aryl migration in α,α-diaryl allylic alcohols toward β-silyl ketones.
A copper-catalyzed radical 1,2-aryl migration in α,α-diaryl allylic alcohols is developed, leading to β-silyl carbonyl compounds in moderate to good yields. The migration of aryls with lower aromaticity is favored. This procedure features the employment of silanes as commercially available materials.
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Silver-catalyzed carbonphosphonation of α,α-diaryl allylic alcohols is achieved. A series of γ-ketophosphonates with different substituents were readily obtained. The mechanistic study indicated that the reaction was initiated by the addition of P-radicals, which sequentially undergo 1,2-migration of an aryl group to form C(Ar)-C(sp(3)) bonds.
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Atomic force microscopy and X-ray diffraction have been used to characterize the structural evolution of the MoO3(010) surface during gas phase reactions with nitrogen-alcohol (methanol, ethanol, and 2-propanol) mixtures between 200 and 400◦C. Our results demonstrate that MoO3 intercalates H during these reactions (T≥ 300◦C) and that protonation leads to the precipitation of a well known hydrog...
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An enantioselective bromoamination of allylic alcohols has been developed for the first time using a newly designed cinchona-derived thiourea as the catalyst and N,N-dibromo-4-nitrobenzenesulfonamide as a bromine and amine source.
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A new dibromination reaction involving the combination of dibromomalonate as the bromonium source and a titanium bromide species as the bromide source has been developed. Enantioselective catalysis has been achieved through apparent ligand acceleration by a tartaric acid-derived diol.
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ژورنال
عنوان ژورنال: Synfacts
سال: 2006
ISSN: 1861-1958,1861-194X
DOI: 10.1055/s-2006-949428