903900-36-7

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 

Downstream Products

• 909543-83-5 (2S,3S,4S,5R)-3,6-anhydro-4-O-benzyl-D-galactitol 

Relevant academic research and scientific papers

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 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

Stereoselective synthesis of highly O-functionalized enantiopure 2,3,4-trisubstituted tetrahydrofurans by tandem debenzylative cyclization of glycal derived 2,3-epoxy alcohols

A new and highly efficient methodology for the construction of synthetically important highly O-functionalized enantiopure 2,3,4-trisubstituted tetrahydrofurans with three contiguous stereocenters is reported. The Royal Society of Chemistry 2006.