methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

Base Information

Chemical Name:methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside
CAS No.:87791-78-4
Molecular Formula:C₁₇H₂₅NO₇
Molecular Weight:355.388
Hs Code.:

Synonyms:methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

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

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Chemical Property of methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

Chemical Property:

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Technology Process of methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

There total 3 articles about methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside 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: 87.0%

: 23445-34-3
methyl 2,3,4-tri-O-methyl-β-D-glucopyranosiduronic acid

: 100-51-6,185532-71-2
benzyl alcohol

: 87791-78-4
methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

Guidance literature:: With diphenyl phosphoryl azide; triethylamine; In benzene; Heating;

Reference yield: 85.0%

: 87791-76-2
methyl 2,3,4-tri-O-methyl-β-D-glucopyranosiduronamide

: 100-51-6,185532-71-2
benzyl alcohol

: 87791-78-4
methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

Guidance literature:: With pyridine; lead(IV) acetate; In benzene; for 4h; Heating;

Reference yield:

: 31506-17-9
methyl (methyl 2,3,4-tri-O-methyl-β-D-glucopyranosid)uronate

: 87791-78-4
methyl (5S)-5-benzyloxycarbonylamino-2,3,4-tri-O-methyl-β-D-xylopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: methanolic ammonia

2: 85 percent / pyridine, lead tetraacetate / benzene / 4 h / Heating

With pyridine; lead(IV) acetate; ammonia; In benzene;