936946-80-4

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 
• 929202-56-2 (2S,3S,4S,5R)-1,2-O-isopropylidene-3,6-anhydro-4-O-benzyl-D-galactitol 
• 124-63-0 methanesulfonyl chloride 

Downstream Products

• 1169393-30-9 1,4-anhydro-2-deoxy-5,6-O-isopropylidene-3-O-benzyl-L-arabino-hex-1-enitol 
• 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 
• 936946-79-1 (2S,3S,4S,5S)-1,2-O-isopropylidene-3,6-anhydro-4-O-benzyl-5-azido-5-deoxy-D-glucitol 

Relevant academic research and scientific papers

Synthesis of enantiomerically pure highly functionalized furanoid glycal and 2,5-Dihydrofuran building blocks

Differently protected enantiomerically pure furanoid glycals (5a-d) and highly functionalized 2,5-dihydrofurans (6a-b) were synthesized from their respective 2,3,4-trisubstituted tetrahydrofurans. These furanoid glycals were identified as 1,4-anhydro-2-de

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.