Highly Enantioselective Synthesis of β-Amino Alcohols: A Catalytic Version
نویسندگان
چکیده
منابع مشابه
Catalytic enantioselective bromoamination of allylic alcohols.
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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The enantioselective oxidative C-H functionalization of tetrahydroisoquinoline derivatives is achieved through the merger of photoredox and asymmetric anion-binding catalysis. This combination of two distinct catalysis concepts introduces a potentially general approach to asymmetric transformations in oxidative photocatalysis.
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ژورنال
عنوان ژورنال: The Journal of Organic Chemistry
سال: 2007
ISSN: 0022-3263,1520-6904
DOI: 10.1021/jo071028x