137410-23-2

Upstream product

• 80040-79-5 3,4,6-tri-O-benzyl-D-galactal 
• 137410-20-9 (2E)-4,6-di-O-benzyl-2,3-dideoxy-aldehydo-D-threo-hex-2-enose 

Downstream Products

• 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 
• 221217-34-1 (2S,3R,4S)-2-Hydroxymethyl-4-((11S,12S)-11-hydroxy-12-methyl-tetradecyl)-1-(toluene-4-sulfonyl)-azetidin-3-ol 

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.

Stereoselective total synthesis of penaresidin A starting from d-galactal

A stereoselective total synthesis of penaresidin A has been accomplished involving Sharpless asymmetric epoxidation, regioselective ring-opening of epoxide, azetidine formation via SN2 reaction, Jung's protocol, and Julia-Kocienski olefination.

Studies on epoxidation of enantiomerically pure 2,3-dideoxy hex-2-enitols: a convenient access to highly functionalized enantiomerically pure tetrahydrofuran derivatives

A detailed comparative study on the epoxidation of enantiomerically pure allylic alcohols 8-14 derived from their respective glycals with Sharpless, m-CPBA and Camp's reagents was carried out in order to obtain 2,3-epoxy alcohols keeping in view the versa

A Convenient Stereoselective Synthesis of D-erythro-C18-Sphingosine from Galactal

The highly efficient stereoselective synthesis of D-erythro-C18-sphingosine from 3,4,6-tribenzyloxygalactal via 4,6-tribenzyloxy-5-hydroxyhexenal is described.