Add to ORKGSynthesis of some novel aminocyclopentitol analogues has been achieved through a functionally embellished cyclopentanoid derivative of well-defined stereochemical disposition, obtained via a Grob-type fragmentation sequence executed within the norbornyl framework. The glycosidase inhibition studies of the new aminocyclopentitols indicate them to be weak inhibitors
A new synthetic approach to diastereomeric cyclopent-3-enylglycines, functionalized on the ring with...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Synthesis of both enantiomers of a highly functionalized cyclopentenol derivative, versatile buildin...
Synthesis of some novel aminocyclopentitol analogues has been achieved through a functionally embell...
A new approach to aminocyclopentitols, leading to a synthesis of trehazolamine analogues is delineat...
A new approach to aminocyclopentitols, leading to a synthesis of trehazolamine analogues is delineat...
A novel fragmentation sequence has been executed within the norbornane system, involving C1–C2 bond ...
A novel fragmentation sequence has been executed within the norbornane system, involving C1-C2 bond ...
An efficient fructose-1,6-bisphosphate aldolase mediated synthesis of new aminocyclitol analogues of...
The behaviour towards the retro-aldol or retro-Dieckmann reactions of several norbornene and norborn...
New syntheses of a range of aminocyclitols, of the aminocarbasugar and ‘confused’ aminocarbasugar ty...
A stereoselective synthesis of new isofagomine analogues has been achieved from a suitably functiona...
A novel fragmentation sequence within the norbornane system, involving C1-C7bond scission, provides ...
Glycosidases are enzymes involved in many biological processes. In consequence, their inhibitors hav...
A new synthesis of deoxynojirimycin (DNJ) analogues (galacto-and altrose configuration) has been ach...
A new synthetic approach to diastereomeric cyclopent-3-enylglycines, functionalized on the ring with...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Synthesis of both enantiomers of a highly functionalized cyclopentenol derivative, versatile buildin...
Synthesis of some novel aminocyclopentitol analogues has been achieved through a functionally embell...
A new approach to aminocyclopentitols, leading to a synthesis of trehazolamine analogues is delineat...
A new approach to aminocyclopentitols, leading to a synthesis of trehazolamine analogues is delineat...
A novel fragmentation sequence has been executed within the norbornane system, involving C1–C2 bond ...
A novel fragmentation sequence has been executed within the norbornane system, involving C1-C2 bond ...
An efficient fructose-1,6-bisphosphate aldolase mediated synthesis of new aminocyclitol analogues of...
The behaviour towards the retro-aldol or retro-Dieckmann reactions of several norbornene and norborn...
New syntheses of a range of aminocyclitols, of the aminocarbasugar and ‘confused’ aminocarbasugar ty...
A stereoselective synthesis of new isofagomine analogues has been achieved from a suitably functiona...
A novel fragmentation sequence within the norbornane system, involving C1-C7bond scission, provides ...
Glycosidases are enzymes involved in many biological processes. In consequence, their inhibitors hav...
A new synthesis of deoxynojirimycin (DNJ) analogues (galacto-and altrose configuration) has been ach...
A new synthetic approach to diastereomeric cyclopent-3-enylglycines, functionalized on the ring with...
Synthesis of nitrogenated quaternary centered polyhydroxylated aminocyclopentanes by implementation ...
Synthesis of both enantiomers of a highly functionalized cyclopentenol derivative, versatile buildin...