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Journal ArticleDOI

Catalytic Asymmetric Allenylation: Regulation of the Equilibrium between Propargyl- and Allenylstannanes during the Catalytic Process.

Chan-Mo Yu, +3 more
- 18 Sep 1998 - 
- Vol. 37, Iss: 17, pp 2392-2395
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TLDR
Achiral substrates 1 and 2 can be regioselectively converted into chiral allenyl alcohols 3 through the title reaction with the synergetic reagent iPrSBEt2 and a chiral TiIV catalyst.
Abstract
Achiral substrates 1 and 2 can be regioselectively converted into chiral allenyl alcohols 3 through the title reaction [Eq. (1)] with the synergetic reagent iPrSBEt2 and a chiral TiIV catalyst. The dramatic regioselectivity originates from the regulation of the equilibrium between propargyl- and allenylstannanes during the catalytic process.

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Journal ArticleDOI

Polysaccharide-based chiral stationary phases for high-performance liquid chromatographic enantioseparation.

TL;DR: A review of polysaccharide-based chiral stationary phases (CSPs) for the direct separation of enantiomers in high-performance liquid chromatography (HPLC) is presented in this article.
Journal ArticleDOI

How easy are the syntheses of allenes

TL;DR: Allenes have proven themselves to be valuable building blocks toward complex molecular targets, revealing novel applications in natural product synthesis, pharmaceutical chemistry and materials science, and some of the recent important developments on the synthesis of allenes are highlighted.
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