14233-52-4

Upstream product

• 4291-69-4 2,3,4,6-Tetra-O-benzyl-D-glucopyranose 
• 14233-49-9 2,3,4,6-tetra-O-benzyl-1-O-trityl-D-glucitol 
• 78136-16-0 2,3,4,6-tetra-O-benzyl-D-glucitol 
• 6564-72-3 2,3,4,6-tetra-O-benzyl-D-glucopyranose 
• 14233-51-3 1,3,4,5-tetra-O-benzyl-6-O-trityl-L-sorbose 

Downstream Products

• 78136-16-0 2,3,4,6-tetra-O-benzyl-D-glucitol 
• 78136-16-0 (2S,3R,4R,5S)-2,3,4,6-tetrakis(benzyloxy)hexane-1,5-diol 
• 1045730-85-5 1,3,4,5-tetra-O-benzyl-6-O-pivaloyl-L-sorbose 
• 14233-51-3 1,3,4,5-tetra-O-benzyl-6-O-trityl-L-sorbose 
• 1045730-67-3 C₄₁H₄₀O₇ 

Relevant academic research and scientific papers

An improved direct conversion of hexoses to hexo-2-uloses

Hexo-2-uloses can be obtained from 2,3,4,6-tetra-O-benzyl-hexopyranoses by an improved procedure employing a Meerwein-Ponndorf-Verley/Oppenauer reaction induced by SmI2/O2/THP as the key step.

Chemical synthesis of 1-deoxy-L-fructose and L-sorbose through carbonyl translocation

Two rare sugars - 1-deoxy-L-fructose and L-sorbose - were synthesized from inexpensive starting materials by a carbonyl translocation method developed in our laboratory. Reduction of a known starting compound gave a 1,5-diol derivative. Selective protecti