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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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Enantioselective alkynylation of aldehydes catalyzed by a camphor sulfonylated amino alcohols titanium(IV) catalyst system

TL;DR: In this paper, a new titanium(IV) complex was developed for the effective enantioselective alkynylation of phenylacetylene addition to aldehydes, which was readily prepared in situ from (R)-C-(7,7-dimethyl-2-oxo-bicyclo[2.2.1]hept-1-yl)-(1R,2S)-N-(2-hydroxy-1,2-diphenyl-ethyl)-methanesulfonamide (1h) and tet
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Synthesis of new Schiff base-camphorsulfonyl amide ligands and in situ screening in the asymmetric additions of organozinc reagents to aldehydes

TL;DR: In this paper, a new library of highly modular Schiff base-camphorsulfonyl amide ligands from readily available starting materials has been designed and synthesized for asymmetric addition of diethyl zinc to aldehydes in good yields and high enantioselectivities.
Reference EntryDOI

Additions of Allyl, Allenyl, and Propargylstannanes to Aldehydes and Imines

TL;DR: The most efficient tools for this strategy include modern aldol reactions and the reaction of carbonyl compounds with allyl metal reagents as discussed by the authors. But these tools are not suitable for the synthesis of polyacetate and polypropionate structures.
Journal ArticleDOI

Recent developments in Zn-catalyzed asymmetric addition reaction to ketones: Syntheses of chiral tertiary alcohols

TL;DR: In this paper, the recent developments of this asymmetric protocol are focused, and a review of the most recent developments can be found in Section 5.1.1] and Section 6.2.
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