142913-85-7

Upstream product

• 100-46-9 benzylamine 
• 23568-31-2 2,3:4,5-di-O-isopropylidene-L-arabinose 
• 142913-83-5 2,3;4,5-di-O-isopropylidene-L-arabinose N-benzylimine 
• 160962-75-4 N-benzyl-(6R,1'S,2'R,3'S)-6-(1',2':3',4'-di-O-isopropylidene-1',2',3',4'-tetrahydroxy-1'-butyl)-2,3-didehydropiperidine-4-one 
• 142913-84-6 N-benzyl-(6S,1'R,2'S,3'R)-6-(1',2':3',4'-di-O-isopropylidene-1',2',3',4'-tetrahydroxy-1'-butyl)-2,3-didehydropiperidine-4-one 

Downstream Products

• 142913-86-8 N-benzyl-(2S,4R,1'R,2'S,3'R)-2-(1',2'-O-isopropylidene-1',2',3',4'-tetrahydroxy-1'-butyl)-4-hydroxypiperidine 
• 142913-86-8 N-benzyl-(2R,4S,1'S,2'R,3'S)-2-(1',2'-O-isopropylidene-1',2',3',4'-tetrahydroxy-1'-butyl)-4-hydroxypiperidine 
• 142913-87-9 (4R,5S)-5-((2R,4S)-1-Benzyl-4-hydroxy-piperidin-2-yl)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 
• 142913-87-9 (4S,5R)-5-((2S,4R)-1-Benzyl-4-hydroxy-piperidin-2-yl)-2,2-dimethyl-[1,3]dioxolane-4-carbaldehyde 

Relevant academic research and scientific papers

Cycloaddition Reactions of Carbohydrate Derivatives. Part V. A Hetero Diels-Alder Approach to Swainsonine Analogs

Diastereoselective hetero Diels-Alder reactions of sugar derived azomethines 4a-4g have been used for the construction of chiral piperidones 6 and 7.Configuration of the major products was 6,1'-threo in every case.The enone system of 6 and 7 was reduced d

Cycloaddition Reactions of Carbohydrate Derivatives. Part III. A New Route to Swainsonine Analogs.

Swainsonine analogs 10 and 12 have been synthesized from D- and L-arabinose, respectively, using cyclocondensation of azomethines with Danisthefsky's diene followed by stereoselective carbonyl and double bond reduction of the resulting pyridones, chain sh