637034-04-9

Upstream product

• 100-46-9 benzylamine 
• 637033-96-6 [3S,4S,5R,6R]-3-O-tert-butyl(dimethyl)silyl-6-formylmethyl-4,5-O-(1-methylethylidene)-3,4,5-trihydroxycyclohexan-1-one 
• 637033-93-3 [3S,4S,5R,6R]-3-O-tert-butyl(dimethyl)silyl-6-tosyloxymethyl-4,5-O-(1-methylethylidene)-3,4,5-trihydroxycyclohexan-1-one 1,3-propanedithioketal 
• 637033-94-4 [3S,4S,5R,6R]-3-O-tert-butyl(dimethyl)silyl-6-cyanomethyl-4,5-O-(1-methylethylidene)-3,4,5-trihydroxycyclohexan-1-one 1,3-propanedithioketal 
• 637033-95-5 [3S,4S,5R,6R]-3-O-tert-butyl(dimethyl)silyl-6-formylmethyl-4,5-O-(1-methylethylidene)-3,4,5-trihydroxycyclohexan-1-one 1,3-propanedithioketal 
• 243978-58-7 [3S,4S,5R,6R]-3-O-tert-butyl(dimethyl)silyl-6-hydroxymethyl-4,5-O-(1-methylethylidene)-3,4,5-trihydroxycyclohexan-1-one 1,3-propanedithioketal 

Relevant academic research and scientific papers

A straightforward route to indolizidine and quinolizidine analogs as new potential antidiabetics

New polyhydroxylated indolizidine and quinolizidine analogs of castanospermine are efficiently obtained by a double reductive amination of enantiopum cyclic ketoaldehydes. As rigidified mimics of disaccharides, these compounds are expected to exhibit sign

Synthesis and glycosidase inhibitory activity of enantiopure polyhydroxylated octahydroindoles and decahydroquinolines, analogs to castanospermine

The synthesis of new enantiopure polyhydroxylated octahydroindoles and decahydroquinolines, analogs to castanospermine, via a double reductive amination of enantiopure cyclic ketoaldehyde, and their inhibitory activity against α- or β-D-glucosidases, α-D-