929202-56-2

Upstream product

• 137410-23-2 (E)-(4R,5R)-4,6-Bis-benzyloxy-hex-2-ene-1,5-diol 
• 137410-20-9 (2E)-4,6-di-O-benzyl-2,3-dideoxy-aldehydo-D-threo-hex-2-enose 
• 80040-79-5 3,4,6-tri-O-benzyl-D-galactal 
• 909543-83-5 (2S,3S,4S,5R)-3,6-anhydro-4-O-benzyl-D-galactitol 
• 67-64-1 acetone 
• 77-76-9 2,2-dimethoxy-propane 

Downstream Products

• 1286680-39-4 C₄₀H₃₈O₆ 
• 1286680-33-8 C₂₀H₂₀O₃ 
• 78151-87-8 (2R,3S,4R)-3,4-bis(benzyloxy)tetrahydrofuran-2-carbaldehyde 
• 916991-43-0 (2R,3S,4R)-3-(benzyloxy)-4-hydroxytetrahydrofuran-2-carbaldehyde 
• 1167439-13-5 C₁₆H₂₁IO₄ 
• 936946-79-1 (2S,3S,4S,5S)-1,2-O-isopropylidene-3,6-anhydro-4-O-benzyl-5-azido-5-deoxy-D-glucitol 
• 936946-81-5 (2S,3S,4S)-4-azido-3-(benzyloxy)-2-((E,Z)-tetradec-1-enyl)tetrahydrofuran 
• 876917-12-3 (2R,3S,4S)-4-azido-3-benzyloxytetrahydrofuran-2-carbaldehyde 
• 936946-80-4 (2S,3S,4S,5R)-1,2-O-isopropylidine-3,6-anhydro-4-O-benzyl-5-O-methane-sulfonyl-D-galactitol 

Relevant academic research and scientific papers

An expedient route for the practical synthesis of pachastrissamine (jaspine B) starting from 3,4,6-tri-O-benzyl-d-galactal

A practically efficient stereoselective synthesis of pachastrissamine (jaspine B) is described starting from 3,4,6-tri-O-benzyl-d-galactal in eight steps and 11% overall yield.

A consecutive approach towards the stereoselective synthesis of trisubstituted THF domains

A highly efficient, consecutive approach for the construction of synthetically valued, enantiomerically pure, trisubstituted THF domains 3-10 in a stereoselective manner starting from glycal derived allylic alcohols 1a-1d under Sharpless asymmetric epoxid