The arylation of bicyclic oxathiane glycosyl donors has been achieved using benzyne generated in situ from 1-aminobenzotriazole (1-ABT) and lead tetraacetate. Following sulfur arylation, glycosylation of acetate ions proceeded with high levels of stereoselectivity to afford α-glycosyl acetates in a ‘one-pot’ reaction, even in the presence of alternative acceptor alcohols
The hetisine-type natural products exhibit one of the most complex carbon skeletons within the diter...
A non-traditional approach to synthesizing aryl vinyl sulfides is described. 2,2-diphenyl-1,3-oxathi...
This paper reports the development of a novel methodology for the catalytic synthesis of aromatic al...
The arylation of bicyclic oxathiane glycosyl donors has been achieved using benzyne generated in sit...
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation st...
The development of a procedure for the one-pot synthesis of glycosyl benzoates directly from unprote...
A bicyclic glycosyl donor is activated as an arylsulfonium ion and used to synthesise alpha-glycosid...
The utility of sulfoxides in a diverse range of transformations in the field of carbohydrate chemist...
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides ...
The reaction of aryl iodides, N‐tert‐butanesulfinamide, and allyl or homoallyl alcohol in the presen...
The ring-opening of 3-aminocyclobutanone oximes enables easy generation of primary alkyl radicals, c...
Carbenium ions generated from substituted benzhydryls using acid catalysis undergo smooth intramolec...
In chemical glycosylation reactions, a glycosyl donor couples with a glycosyl acceptor through glyco...
The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoter...
Carbohydrates play a pivotal role in biological systems and present an opportunity to develop potent...
The hetisine-type natural products exhibit one of the most complex carbon skeletons within the diter...
A non-traditional approach to synthesizing aryl vinyl sulfides is described. 2,2-diphenyl-1,3-oxathi...
This paper reports the development of a novel methodology for the catalytic synthesis of aromatic al...
The arylation of bicyclic oxathiane glycosyl donors has been achieved using benzyne generated in sit...
Novel oxathiane spiroketal donors have been synthesised and activated via an umpolung S-arylation st...
The development of a procedure for the one-pot synthesis of glycosyl benzoates directly from unprote...
A bicyclic glycosyl donor is activated as an arylsulfonium ion and used to synthesise alpha-glycosid...
The utility of sulfoxides in a diverse range of transformations in the field of carbohydrate chemist...
A conceptionally novel nucleophilic substitution approach to synthetically important alkyl bromides ...
The reaction of aryl iodides, N‐tert‐butanesulfinamide, and allyl or homoallyl alcohol in the presen...
The ring-opening of 3-aminocyclobutanone oximes enables easy generation of primary alkyl radicals, c...
Carbenium ions generated from substituted benzhydryls using acid catalysis undergo smooth intramolec...
In chemical glycosylation reactions, a glycosyl donor couples with a glycosyl acceptor through glyco...
The use of (salen)Co catalysts as a new class of bench-stable stereoselective glycosylation promoter...
Carbohydrates play a pivotal role in biological systems and present an opportunity to develop potent...
The hetisine-type natural products exhibit one of the most complex carbon skeletons within the diter...
A non-traditional approach to synthesizing aryl vinyl sulfides is described. 2,2-diphenyl-1,3-oxathi...
This paper reports the development of a novel methodology for the catalytic synthesis of aromatic al...
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