Add to ORKGTwo anomeric spirodiketopiperazines and one spirohydantoin of 6-deoxy-l-lyxofuranose have been prepared from l-fucono-δ-lactone via ring contraction to the corresponding tetrahydrofuran carboxylate and anomeric functionalization including regioselective bromination and azide displacement. © 2006 Elsevier Ltd. All rights reserved
A new and efficient three-step procedure for the synthesis of 1,6-anhydro-α-D-galactofuranose is des...
Spironucleosides are a type of conformationally restricted nucleoside analogs in which the anomeric ...
International audienceHerein we investigate the scope and limitations of a new synthetic approach to...
Bromine-induced oxidative ring contraction of an α-amino-δ-lactone gave a mixture of α-aminotetrahyd...
The first synthesis of a spirodiketopiperazine at the anomeric carbon of a pyranose sugar is describ...
Epimeric mannofuranose anomeric aminoesters are prepared from readily available azidolactones and ca...
A series of sugar-derived spiroaminals has been synthesized by utilizing cross metathesis, ring clos...
An approach to the synthesis of D-mannopyranose derivatives incorporating an anomeric α-amino acid c...
A general route for the synthesis of tetrahydrofuran α-azido esters as the equivalent of monomeric f...
The first syntheses of two diketopiperazine peptides containing an α-amino in which the α-carbon is ...
Tetrahydropyran and tetrahydrofuran containing natural products, drugs and agrochemicals often posse...
An α-azidocarboxylate of a tetrahydrofuran derived from L-rhamnose may be used as a divergent interm...
The multi-gram syntheses of two epimeric six-carbon tetrahydrofurancarboxylates based upon a D-arabi...
Epimeric azidoesters containing a glucofuranosyl moiety are readily prepared from glucoheptonolacton...
A new and efficient approach for direct and stereoselective synthesis of β‐mannopyranosides by anome...
A new and efficient three-step procedure for the synthesis of 1,6-anhydro-α-D-galactofuranose is des...
Spironucleosides are a type of conformationally restricted nucleoside analogs in which the anomeric ...
International audienceHerein we investigate the scope and limitations of a new synthetic approach to...
Bromine-induced oxidative ring contraction of an α-amino-δ-lactone gave a mixture of α-aminotetrahyd...
The first synthesis of a spirodiketopiperazine at the anomeric carbon of a pyranose sugar is describ...
Epimeric mannofuranose anomeric aminoesters are prepared from readily available azidolactones and ca...
A series of sugar-derived spiroaminals has been synthesized by utilizing cross metathesis, ring clos...
An approach to the synthesis of D-mannopyranose derivatives incorporating an anomeric α-amino acid c...
A general route for the synthesis of tetrahydrofuran α-azido esters as the equivalent of monomeric f...
The first syntheses of two diketopiperazine peptides containing an α-amino in which the α-carbon is ...
Tetrahydropyran and tetrahydrofuran containing natural products, drugs and agrochemicals often posse...
An α-azidocarboxylate of a tetrahydrofuran derived from L-rhamnose may be used as a divergent interm...
The multi-gram syntheses of two epimeric six-carbon tetrahydrofurancarboxylates based upon a D-arabi...
Epimeric azidoesters containing a glucofuranosyl moiety are readily prepared from glucoheptonolacton...
A new and efficient approach for direct and stereoselective synthesis of β‐mannopyranosides by anome...
A new and efficient three-step procedure for the synthesis of 1,6-anhydro-α-D-galactofuranose is des...
Spironucleosides are a type of conformationally restricted nucleoside analogs in which the anomeric ...
International audienceHerein we investigate the scope and limitations of a new synthetic approach to...