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Asymmetric alkynylation of aldehydes with propiolates without high reagent loading and any additives†
Naoto Kojima,Shogo Nishijima,Kaoru Tsuge,Tetsuaki Tanaka
Organic & Biomolecular Chemistry Pub Date : 04/21/2011 00:00:00 , DOI:10.1039/C1OB05489A
Abstract

The asymmetric alkynylation of aliphatic and aromatic aldehydes with propiolates was mediated by dialkylzinc and a novel prolinol catalyst without high reagent loading and any additives, such as Ti(Oi-Pr)4, to give the corresponding γ-hydroxy-α,β-acetylenic esters with high enantiomeric excess of up to 95%.

Graphical abstract: Asymmetric alkynylation of aldehydes with propiolates without high reagent loading and any additives
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