Chiral glycolic acid equivalents are used extensively for the enantioselective synthesis of α-hydroxycarbonyl compounds. Their efficacy in enolate reactions and their utility in synthetic applications are discussed, highlighting the relevance of these methods to natural product synthesis
The preparation of butane-2,3-diacetal protected glycolic acid and related systems is described toge...
This article covers N-acyl chiral auxiliary-based approaches to the asymmetric synthesis of enantiop...
Consecutive coupling reactions of butane-2,3-diacetal protected glycolic acid derivatives with Micha...
According to a chiral memory protocol, a chiral glycolic acid equivalent, the butane-2,3-diacetal-de...
(S)-[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl](4-methoxyphenyl)methanol (4b) has been synthesized and eva...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
Typescript (photocopy).The formation of a new carbon-carbon bond is perhaps the most fundamental rea...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
Asymmetric synthesis has emerged as one of the most rap-idly developing research areas in organic ch...
Abstract: Triphenylglycol-derived esters 2 and 8a have been applied in asymmetric aldol reactions. T...
A benzyloxycarbonyl protected glycine equivalent 2 has been prepared in enantiopure form and has bee...
Enantioselective propionate alkylation, as a method to control acyclic methyl~bearing stereocenters,...
The research, to be discussed in three chapters, involves the development of new synthetic methods w...
An efficient three-step method has been developed for enantioselective synthesis of chiral α-aminoxy...
The preparation of butane-2,3-diacetal protected glycolic acid and related systems is described toge...
This article covers N-acyl chiral auxiliary-based approaches to the asymmetric synthesis of enantiop...
Consecutive coupling reactions of butane-2,3-diacetal protected glycolic acid derivatives with Micha...
According to a chiral memory protocol, a chiral glycolic acid equivalent, the butane-2,3-diacetal-de...
(S)-[(4R)-2,2-Dimethyl-1,3-dioxolan-4-yl](4-methoxyphenyl)methanol (4b) has been synthesized and eva...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
Typescript (photocopy).The formation of a new carbon-carbon bond is perhaps the most fundamental rea...
The aldol reaction is one of the most important carbon–carbon bond formations in synthetic organic c...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
Asymmetric synthesis has emerged as one of the most rap-idly developing research areas in organic ch...
Abstract: Triphenylglycol-derived esters 2 and 8a have been applied in asymmetric aldol reactions. T...
A benzyloxycarbonyl protected glycine equivalent 2 has been prepared in enantiopure form and has bee...
Enantioselective propionate alkylation, as a method to control acyclic methyl~bearing stereocenters,...
The research, to be discussed in three chapters, involves the development of new synthetic methods w...
An efficient three-step method has been developed for enantioselective synthesis of chiral α-aminoxy...
The preparation of butane-2,3-diacetal protected glycolic acid and related systems is described toge...
This article covers N-acyl chiral auxiliary-based approaches to the asymmetric synthesis of enantiop...
Consecutive coupling reactions of butane-2,3-diacetal protected glycolic acid derivatives with Micha...
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