ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

Base Information

Chemical Name:ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate
CAS No.:1225441-86-0
Molecular Formula:C₂₀H₂₆O₇
Molecular Weight:378.422
Hs Code.:

Synonyms:ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

Suppliers and Price of ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

There total 1 articles about ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 43.0%

: 23558-05-6
3-O-benzyl-1,2-O-isopropylidene-1,5-D-xylo-dialdofuranose

: 140-88-5,9003-32-1
ethyl acrylate

: 1225441-87-1
ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-α-D-gluco-1,4-hepto-furanoate

: 1225441-86-0
ethyl 3-O-benzyl-6-deoxy-6-methylene-1,2-O-isopropylidene-β-L-ido-1,4-hepto-furanoate

Guidance literature:: With 1,4-diaza-bicyclo[2.2.2]octane; In 1,4-dioxane; water; at 30 ℃; for 48h; Inert atmosphere;
DOI:10.1016/j.tet.2010.02.044