This review covers further applications of the conjugate addition of enantiomerically pure lithium amides as chiral ammonia equivalents in asymmetric synthesis and provides an update since our last review of this area, which was published in 2012
The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The ...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
This review covers further applications of the conjugate addition of enantiomerically pure lithium a...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This thesis is concerned with the application of the conjugate addition of enantiopure secondary lit...
The addition products from the highly stereoselective conjugate additions of lithium (αS)-(α-methylb...
This thesis describes the use of chiral lithium amides as enantiotopic deprotonating agents and as n...
The addition products from the highly stereoselective conjugate additions of lithium (αS)-(α-methylb...
This thesis describes the use of chiral lithium amides as enantiotopic deprotonating agents and as n...
An overview on the structural arrangements adopted by Chiral Lithium Amides (CLAs), alone or in mixe...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
Chiral lithium amide bases allow the desymmetrisation of prochiral substrates and the production of ...
The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The ...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
This review covers further applications of the conjugate addition of enantiomerically pure lithium a...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This review delineates the scope and limitations of the conjugate addition of homochiral lithium ami...
This thesis is concerned with the application of the conjugate addition of enantiopure secondary lit...
The addition products from the highly stereoselective conjugate additions of lithium (αS)-(α-methylb...
This thesis describes the use of chiral lithium amides as enantiotopic deprotonating agents and as n...
The addition products from the highly stereoselective conjugate additions of lithium (αS)-(α-methylb...
This thesis describes the use of chiral lithium amides as enantiotopic deprotonating agents and as n...
An overview on the structural arrangements adopted by Chiral Lithium Amides (CLAs), alone or in mixe...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
Chiral lithium amide bases allow the desymmetrisation of prochiral substrates and the production of ...
The conjugate addition reaction has been a useful tool in the formation of carbon–carbon bonds. The ...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...
International audienceAn overview on the structural arrangements adopted by Chiral Lithium Amides (C...