134590-58-2

Upstream product

• 63598-31-2 methyl 4,6-O-(R)-benzylidene-2-deoxy-α-D-erythrohexopyranosid-3-ulose 
• 73395-15-0 methyl endo(phenyl)-2,3:4,6-di-O-benzylidene-α-D-mannopyranoside 
• 122672-65-5 methyl 2-deoxy-2-(2-ethoxy-2-oxoethyl)-4,6-O-(phenylmethylene)-α-D-ribohexopyranosid-3-ulose 
• 134622-79-0 methyl 2-deoxy-2-(2-ethoxy-2-oxoethyl)-4,6-O-(phenylmethylene)-α-D-allopyranoside 
• 130781-46-3 methyl 2-deoxy-2-(2-oxoethyl)-4,6-O-(phenylmethylene)-α-D-allopyranoside 2',3 lactone 
• 74-88-4 methyl iodide 

Relevant academic research and scientific papers

General Synthesis of Homochiral Trisubstituted γ-Butyrolactones

The synthetically useful keto ester methyl 2-deoxy-2-(2-ethoxy-2-oxoethyl)-4,6-O-(phenylmethylene)-α-D-ribo-hexopyranosid-3-ulose can be prepared exclusively by reaction of the potassium enolate of methyl 2-deoxy-4,5-O-(phenylmethylene)-α-D-erythro-hexopy

Synthesis of homochiral trisubstituted γ-butyrolactones

Efficient syntheses of homochiral, trisubstituted γ-butyrolactones via the highly stereoselective alkylation of a carbohydrate-derived γ-lactone are described.