Add to ORKGThe only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconojirimycin [1,5-dideoxy-1,5-imino-L- fucitol] from D-lyxonolactone, a readily available chiral pool material, is a single isopropylidene group
Both enantiomers of isofagomine, the potent glycosidase inhibitor of a type 1-N-iminosugar have been...
A new and stereoselective strategy is developed to synthesize an appropriate template 9 to obtain C-...
A rigid bicyclic analogue of α-L-fucose, prepared from a monoacetonide of L-gulonolactone in an over...
The only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconoji...
The only protection required in a five-step synthesis of the a-L-fucosidase inhibitor, deoxyfuconoji...
Deoxyfuconojirimycin (1,5-dideoxy-1,5-imino-L-fucitol) is a potent, specific and competitive inhibit...
1,6-Dideoxygalactostatin, the mirror image of 1-deoxy-L-fuconojirimycin, was efficiently prepared fr...
The total synthesis of enantiopure 4-epi-(+)-codonopsinine was achieved in 10 steps starting from d-...
1,6-Dideoxygalactostatin, the mirror image of 1-deoxy-L-fuconojirimycin, was efficiently prepared fr...
1,5-Dideoxy-1,5-imino-l-fucitol (1-deoxyfuconojirimycin, DFJ) is an iminosugar that inhibits fucosid...
1,5-Dideoxy-1,5-imino-L-fucitol (1), synthesised from methyl α-D-glucopyranoside, is a potent compet...
A diversity-oriented synthesis is described for functionalized chiral building blocks (i.e., 7, 9, 1...
Eight configurational 1-deoxynojirimycin isomers have been synthesized starting from a chiral cyanoh...
Bioisosteric modification of known fucosidase inhibitors A and B, resulted in three new types of mol...
The difluoromethyl-allo-threonyl hydroxamate-based compound LPC-058 is a potent inhibitor of UDP-3-O...
Both enantiomers of isofagomine, the potent glycosidase inhibitor of a type 1-N-iminosugar have been...
A new and stereoselective strategy is developed to synthesize an appropriate template 9 to obtain C-...
A rigid bicyclic analogue of α-L-fucose, prepared from a monoacetonide of L-gulonolactone in an over...
The only protection required in a five-step synthesis of the α-L-fucosidase inhibitor, deoxyfuconoji...
The only protection required in a five-step synthesis of the a-L-fucosidase inhibitor, deoxyfuconoji...
Deoxyfuconojirimycin (1,5-dideoxy-1,5-imino-L-fucitol) is a potent, specific and competitive inhibit...
1,6-Dideoxygalactostatin, the mirror image of 1-deoxy-L-fuconojirimycin, was efficiently prepared fr...
The total synthesis of enantiopure 4-epi-(+)-codonopsinine was achieved in 10 steps starting from d-...
1,6-Dideoxygalactostatin, the mirror image of 1-deoxy-L-fuconojirimycin, was efficiently prepared fr...
1,5-Dideoxy-1,5-imino-l-fucitol (1-deoxyfuconojirimycin, DFJ) is an iminosugar that inhibits fucosid...
1,5-Dideoxy-1,5-imino-L-fucitol (1), synthesised from methyl α-D-glucopyranoside, is a potent compet...
A diversity-oriented synthesis is described for functionalized chiral building blocks (i.e., 7, 9, 1...
Eight configurational 1-deoxynojirimycin isomers have been synthesized starting from a chiral cyanoh...
Bioisosteric modification of known fucosidase inhibitors A and B, resulted in three new types of mol...
The difluoromethyl-allo-threonyl hydroxamate-based compound LPC-058 is a potent inhibitor of UDP-3-O...
Both enantiomers of isofagomine, the potent glycosidase inhibitor of a type 1-N-iminosugar have been...
A new and stereoselective strategy is developed to synthesize an appropriate template 9 to obtain C-...
A rigid bicyclic analogue of α-L-fucose, prepared from a monoacetonide of L-gulonolactone in an over...