International audienceIn this paper, a new access to several chiral 3-aminoglycals as potential precursors for glycosylated natural products is reported from a common starting material, (-)-methyl-L-lactate. The stereodivergent strategy is based on the implementation of a ring-closing metathesis of vinyl ethers as key step of reaction sequences developed
This thesis is divided into three separate parts with amino alcohols as the common feature. The firs...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
The stereoselective synthesis of alpha-C-glycosides of D-glucosainine, through a procedure which inv...
International audienceIn this paper, a new access to several chiral 3-aminoglycals as potential prec...
Enantiomerically pure t-Butyl 2-amino-2,5-dideoxy---pentanoate 4c is synthesized via the highly dias...
International audienceThe nitro-Michael addition of organolithium species to 2 nitroglycal derivativ...
Various isomers of C6-methyl-containing chiral 3,4-dideoxy furanoid sugar amino acids were synthesiz...
Diastereoselective control of glycosylation still remains a difficult task. Therefore, new glycosyla...
The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one ...
The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one ...
International audienceA stereospecific Mizoroki-Heck cross-coupling of differently substituted glyca...
A procedure for the synthesis ofL-IX-vinylglycine from L-homoserine lactone is described. The route ...
Abstract: Enantiomerically pure homoallyl amines and ~amino acids are synthesized using the diastere...
One of the goals of diversity-oriented synthesis is to achieve the structural diversity of obtained ...
This is the first report on the diastereoselective addition of carbon nucleophiles to vinyl sulfone-...
This thesis is divided into three separate parts with amino alcohols as the common feature. The firs...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
The stereoselective synthesis of alpha-C-glycosides of D-glucosainine, through a procedure which inv...
International audienceIn this paper, a new access to several chiral 3-aminoglycals as potential prec...
Enantiomerically pure t-Butyl 2-amino-2,5-dideoxy---pentanoate 4c is synthesized via the highly dias...
International audienceThe nitro-Michael addition of organolithium species to 2 nitroglycal derivativ...
Various isomers of C6-methyl-containing chiral 3,4-dideoxy furanoid sugar amino acids were synthesiz...
Diastereoselective control of glycosylation still remains a difficult task. Therefore, new glycosyla...
The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one ...
The conceptually simple process of linking carbohydrate units by glycosylation has proven to be one ...
International audienceA stereospecific Mizoroki-Heck cross-coupling of differently substituted glyca...
A procedure for the synthesis ofL-IX-vinylglycine from L-homoserine lactone is described. The route ...
Abstract: Enantiomerically pure homoallyl amines and ~amino acids are synthesized using the diastere...
One of the goals of diversity-oriented synthesis is to achieve the structural diversity of obtained ...
This is the first report on the diastereoselective addition of carbon nucleophiles to vinyl sulfone-...
This thesis is divided into three separate parts with amino alcohols as the common feature. The firs...
A new chiral glycine equivalent 7 has been synthesised from glycidol using a chiral memory protocol,...
The stereoselective synthesis of alpha-C-glycosides of D-glucosainine, through a procedure which inv...