Catalytic asymmetric nucleophilic additions to carbonyls and imines, as well as conjugate additions to Michael acceptors are powerful methods for carbon-carbon bond formation. Applications for a variety of nucleophiles have been reported in the past few years. This chapter surveys the most recent developments with a particular focus on work using non-stabilized nucleophiles, such as organomagnesium (Grignard), organozinc, organoboron, organozirconium, and organotitanium reagents. The literature from the last five years is covered, with a selection of important references from before 2015 included as background information. The chapter is divided into three parts: (i) asymmetric nucleophilic addition to ketones, (ii) asymmetric nucleophilic ...
On the basis of the investigation of the combinational effect of quaternary ammonium salts and organ...
Abstract: The Michael additions of a number of ketones and alde-hydes to alkylidene malonates and ni...
The development of new methods for carbon-carbon bond formation is a challenging topic at the heart ...
Catalytic asymmetric nucleophilic additions to carbonyls and imines, as well as conjugate additions ...
There is a growing need in organic synthesis for efficient methodologies for the asymmetric synthesi...
The research described in this thesis is primarily aimed at exploring challenging substrates for Cu-...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
The conjugateadditionreaction is a fundamental process in organic chemistry. The reaction involves t...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A review of catalytic asym. conjugate addn. reactions using organometallic reagents. [on SciFinder(R...
The scope and stereochemistry of nucleophilic addition of Grignard reagents and silyl ketene acetals...
A review of catalytic asym. conjugate addn. reactions using organometallic reagents. [on SciFinder(R...
[[abstract]]The nucleophilic addition of a Grignard reagent or organolithium compound to the carbony...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
This thesis is concerned with the asymmetric conjugate addition reactions of a range of chiral nuclo...
On the basis of the investigation of the combinational effect of quaternary ammonium salts and organ...
Abstract: The Michael additions of a number of ketones and alde-hydes to alkylidene malonates and ni...
The development of new methods for carbon-carbon bond formation is a challenging topic at the heart ...
Catalytic asymmetric nucleophilic additions to carbonyls and imines, as well as conjugate additions ...
There is a growing need in organic synthesis for efficient methodologies for the asymmetric synthesi...
The research described in this thesis is primarily aimed at exploring challenging substrates for Cu-...
This thesis is concerned with the design, synthesis and use of novel bifunctional organocatalysts fo...
The conjugateadditionreaction is a fundamental process in organic chemistry. The reaction involves t...
The 1,4-conjugate addition of nucleophiles to \u3b1,\u3b2-unsaturated carbonyl compounds represents ...
A review of catalytic asym. conjugate addn. reactions using organometallic reagents. [on SciFinder(R...
The scope and stereochemistry of nucleophilic addition of Grignard reagents and silyl ketene acetals...
A review of catalytic asym. conjugate addn. reactions using organometallic reagents. [on SciFinder(R...
[[abstract]]The nucleophilic addition of a Grignard reagent or organolithium compound to the carbony...
All-carbon quaternary stereocenters are ubiquitous motifs in biological products and pharmaceutical ...
This thesis is concerned with the asymmetric conjugate addition reactions of a range of chiral nuclo...
On the basis of the investigation of the combinational effect of quaternary ammonium salts and organ...
Abstract: The Michael additions of a number of ketones and alde-hydes to alkylidene malonates and ni...
The development of new methods for carbon-carbon bond formation is a challenging topic at the heart ...