710965-66-5

Upstream product

• 710965-65-4 (S)-((2R,3R,4R,5S,6R)-4,5-Bis-benzyloxy-6-benzyloxymethyl-2-methoxy-tetrahydro-pyran-3-yl)-iodo-acetic acid methyl ester 
• 55628-54-1 3,4,6-tri-O-benzyl-D-glucal 
• 710965-64-3 1,5-anhydro-2-deoxy-2-C-(exo-carbomethoxymethylene)-3,4,6-tri-O-benzyl-α-D-glucitol 
• 946512-99-8 methyl 3,4,6-tri-O-benzyl-2-deoxy-2-C-[(methoxycarbonyl)methyl]-β-D-glucopyranoside 

Relevant academic research and scientific papers

Stereoselective diversity-oriented syntheses of functionalized saccharides from bicyclic carbohydrate 1,2-lactones

Bicyclic carbohydrate 1,2-lactones have been synthesized in only two steps and high yields by saponification and subsequent cyclization from known malonate addition products to glycals. The gluco-configured lactone serves as an important precursor for div

Stereodivergent syntheses at the glucose backbone

Both diastereomers of 2-C-branched carbohydrates with various functional groups are selectively available from the same malonate precursor in good yields in only a few steps. The Royal Society of Chemistry 2009.

Efficient methodology for the synthesis of 2-C-branched glyco-amino acids by ring opening of 1,2-cyclopropanecarboxylated sugars

Matrix presented. An efficient methodology for the synthesis of 2-C-branched glyco-amino acid derivatives by diastereoselective ring opening of 1,2-cyclopropanecarboxylated sugars in good yields is reported.