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- W149720922 abstract "Optically active propargylic alcohols and propargylamines are highly useful and versatile building blocks. One of the most common approaches to these compounds is the catalytic asymmetric alkynylation of carbonyl compounds and imines. Various combinations of chiral ligands and metal catalysts have been examined and several highly efficient asymmetric catalysts have been developed so far. Although stoichiometric amounts of metal reagents were used for this type of reaction in the earliest stages of development, direct in situ generation of a metal alkynylide species from terminal alkynes with a catalytic amount of the metal reagent is currently a major interest in organic synthesis. This article summarizes catalytic asymmetric 1,2-alkynylation of aldehydes, ketones, aldimines and ketimines with respect to the use of either stoichiometric or catalytic amounts of metal reagents." @default.
- W149720922 created "2016-06-24" @default.
- W149720922 creator A5017628553 @default.
- W149720922 creator A5025752165 @default.
- W149720922 creator A5034960043 @default.
- W149720922 date "2015-01-01" @default.
- W149720922 modified "2023-09-25" @default.
- W149720922 title "Catalytic Asymmetric 1,2-Alkynylation☆" @default.
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