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Catalytic asymmetric induction. Highly enantioselective addition of dialkylzincs to aldehydes

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This article is published in Journal of the American Chemical Society.The article was published on 1986-09-01. It has received 479 citations till now. The article focuses on the topics: Addition reaction & Enantioselective synthesis.

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Zn(ODf)2: preparation and application in asymmetric alkynylation of aldehydes.

TL;DR: A new Lewis acid, Zn(ODf)2, was first prepared from commercially available 3,3,4,4-tetrafluoro[1,2]oxathietane 2,2-dioxide in four steps with 56% yields and also was applied to catalyze highly enantioselective alkynylation of aldehydes.
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Catalytic enantioselective alkyl and aryl addition to aldehydes and ketones with organozinc reagents derived from alkyl Grignard reagents or arylboronic acids

TL;DR: A highly practical, catalytic enantioselective alkyl and aryl addition to aldehydes and ketones with organozinc reagents, which were prepared in situ from commercially available Grignard reagents or aryalboronic acids.
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Vanadium‐Catalyzed Asymmetric Oxidation of Sulfides Using Schiff Base Ligands Derived from β‐Amino Alcohols with Two Stereogenic Centers

TL;DR: In this paper, a new Schiff base ligands derived from β-amino alcohols with two stereogenic centers were used in the preparation of optically pure sulfoxides by using aqueous hydrogen peroxide as the oxidant.
Journal ArticleDOI

Catalytic asymmetric synthesis of chiral diol, bis[2-(1-hydroxyalkyl)-phenyl]ether, an asymmetric autocatalytic reaction

TL;DR: In this paper, Zinc alkoxides of chiral diols were found to work as asymmetric autocatalysts in the reaction between bis(2-formylphenyl)ether and dialkylzincs.
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