There is a growing need in organic synthesis for efficient methodologies for the asymmetric
synthesis of quaternary carbon centres. One of the most attractive and straightforward …

Enantioselective catalytic formation of tertiary stereogenic centers has nowadays reached
an impressive level of maturity, as is reflected in the large variety of available methods that …

Efficient tertiary alcohol synthesis is currently one of the most rapidly advancing fields in
organic chemistry, and recent powerful catalytic methodologies can provide versatile tertiary …

A good choice: A new catalytic method was found for the construction of stereogenic
quaternary carbon centers through a copper-catalyzed domino conjugated reduction/aldol …

Asymmetric Autocatalysis Enables an Improved Synthesis of Efavirenz × Close The Infona
portal uses cookies, ie strings of text saved by a browser on the user's device. The portal can …

The asymmetric addition of terminal ynamides to trifluoromethyl ketones with a readily
available chiral zinc catalyst gives CF3‐substituted tertiary propargylic alcohols in up to 99 …

Cooperative catalysis, inspired by the early findings on enzymatic activation, is a fast
growing research area. It refers to the combination of two or more catalytic species that …

A broad range of tertiary propargylic alcohols were kinetically resolved by catalyst‐
controlled enantioselective silylation. This non‐enzymatic kinetic resolution is catalyzed by a …

Carbon-carbon bond forming reactions are simple and direct methods for synthesizing the
various skeletons and the diverse structures of organic compounds. Even 100 years after the …

Cation‐binding salen nickel catalysts were developed for the enantioselective alkynylation
of trifluoromethyl ketones in high yield (up to 99%) and high enantioselectivity (up to 97 …