780782-25-4

Upstream product

• 780782-23-2 (3R,4R,5R)-N-tert-butoxycarbonyl-3-(tert-butyldiphenylsilyloxy)-4,5-epoxypiperidine 
• 1112-56-7 tetravinyltin (IV) 
• 58479-61-1 tert-butylchlorodiphenylsilane 
• 780782-28-7 tert-butyl (S)-3-hydroxy-3,6-dihydropyridine-1(2H)-carboxylate 
• 780782-22-1 (S)-N-tert-butoxycarbonyl-5-(tert-butyldiphenylsilyloxy)-3-piperidene 

Downstream Products

• 169105-89-9 isofagomine 
• 858614-82-1 (3R,4R,5S)-N-tert-butoxycarbonyl-3-(tert-butyldiphenylsilyloxy)-4-hydroxy-5-(hydroxymethyl)piperidine 
• 858614-84-3 (3R,4R,5S)-N-tert-butoxycarbonyl-3-(tert-butyldiphenylsilyloxy)-4-hydroxy-5-(2-hydroxyethyl)piperidine 

Relevant academic research and scientific papers

A new route to diverse 1-azasugars from N-Boc-5-hydroxy-3-piperidene as a common building block

A new general method for the synthesis of a variety of 1-azasugars with a nitrogen atom at the anomeric position is described. The readily available chiral N-Boc-5-hydroxy-3-piperidene 3 is transformed to isofagomine (2), homoisofagomine (13), and 5′-deox

A short and concise synthesis of isofagomine, homoisofagomine, and 5′-deoxyisofagomine

A short and concise synthesis of isofagomine derivatives via the epoxidation of chiral N-Boc-5-hydroxy-3-piperidene, followed by regioselective epoxide ring opening is described. This constitutes the first reported synthesis of homoisofagomine and the 5′-