trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside

Base Information

Chemical Name:trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside
CAS No.:105592-48-1
Molecular Formula:C₈₈H₉₂N₂O₂₉
Molecular Weight:1644.67
Hs Code.:

trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside

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Chemical Property of trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside

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Technology Process of trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside

There total 1 articles about trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside 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:

: Acetic acid (2R,3S,4R,5R,6S)-3-acetoxy-2-acetoxymethyl-6-bromo-5-(1,3-dioxo-1,3-dihydro-isoindol-2-ylamino)-tetrahydro-pyran-4-yl ester

: 105608-14-8
trideuteriomethyl O-(3,4-di-O-benzyl-α-D-mannopyranosyl)-(1->6)-2,3,4-tri-O-benzyl-β-D-mannopyranoside

: 105592-48-1
trideuteriomethyl 2,3,4-tri-O-benzyl-6-O-<3,4-di-O-benzyl-2,6-di-O-(3,4,6-tri-O-acetyl-2-deoxy-2-phthalimido-β-D-glucopyranosyl)-α-D-mannopyranosyl>-β-D-mannopyranoside

Guidance literature:: With 4 A molecular sieve; silver trifluoromethanesulfonate; Yield given. Multistep reaction; 1.) acetonitrile, 5 m, -30 deg C, 2.) acetonitrile, room temperature;
DOI:10.1016/S0008-6215(00)90207-6