6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate

Base Information

Chemical Name:6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate
CAS No.:1190921-25-5
Molecular Formula:C₄₂H₄₉N₃O₁₃
Molecular Weight:803.863
Hs Code.:

Synonyms:6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate

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Chemical Property of 6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate

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Technology Process of 6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate

There total 1 articles about 6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate 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: 70.0%

: 1208105-46-7
C₃₁H₃₃N₃O₆S

: 444118-44-9
1,2-O-isopropylidene-3-O-benzyl-4-O-trichloroacetyl-6-methyl-α-L-idonic acid

: 1190921-25-5
6-O-benzyl-2-azido-3-O-benzyl-2-deoxy-4-O-Lev-α-D-glucopyranosyl-(1->4)-methyl 3-O-benzyl-1,2-O-isopropylidene-β-L-idopyranosuronate

Guidance literature:: C₃₁H₃₃N₃O₆S; 1,2-O-isopropylidene-3-O-benzyl-4-O-trichloroacetyl-6-methyl-α-L-idonic acid; In dichloromethane; at 0 ℃; Molecular sieve; Inert atmosphere;

With N-iodo-succinimide; In dichloromethane;

With silver trifluoromethanesulfonate; In dichloromethane; stereoselective reaction;
DOI:10.1021/ol901723m