1403589-77-4

Upstream product

• 1231913-19-1 (S)-2-(1,4-dioxaspiro[4.5]decan-2-yl)-pent-4-enal 
• 1339946-62-1 (R)-2-((S)-1,4-dioxaspiro[4.5]decan-2-yl)-pent-4-en-1-ol 
• 100-39-0 benzyl bromide 

Downstream Products

• 1354578-72-5 (2S,3R)-3-(benzyloxymethyl)-hex-5-ene-1,2-diol 
• 1071070-15-9 C₁₃H₁₆O₂ 
• 95791-03-0 (2S)-2-[(benzyloxy)methyl]pent-4-en-1-ol 
• 1403589-80-9 (S)-2-((R,E)-5-azido-1-(benzyloxy)pent-3-en-2-yl)-1,4-dioxaspiro[4.5]decane 
• 1403589-81-0 (S)-2-((R)-1-((2R,3R)-3-(azidomethyl)-1,4-dioxaspiro[4.5]decan-2-yl)-2-(benzyloxy)ethyl)-1,4-dioxaspiro[4.5]decane 
• 169105-89-9 isofagomine 
• 1403589-82-1 C₂₀H₂₉N₃O₅ 
• 1403589-78-5 (R,E)-5-(benzyloxy)-4-((S)-1,4-dioxaspiro[4.5]decan-2-yl)pent-2-en-1-yl acetate 
• 1429631-96-8 (R)-5-(benzyloxy)-4-((S)-1,4-dioxaspiro[4.5]decan-2-yl)pentan-2-one 

Relevant academic research and scientific papers

Synthesis of (+)-isofagomine

The synthesis of (+)-isofagomine 1 using 4-pentenol 3 as a chiral precursor is described herein.

A stereodivergent approach to carbahexofuranoses: Synthesis of carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-allofuranose, carba-β-d-idofuranose, carba-α-d- galactofuranose and carba-β-d-talofuranose

A stereodivergent route, starting from d-glyceraldehyde derivative, employing Wittig olefination-Claisen rearrangement protocol is reported for the synthesis of six novel carbahexofuranoses - carba-α-d-glucofuranose, carba-β-d-altrofuranose, carba-α-d-all