phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

Base Information

Chemical Name:phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside
CAS No.:1227637-18-4
Molecular Formula:C₆₁H₇₀O₁₅S
Molecular Weight:1075.28
Hs Code.:

Synonyms:phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

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Chemical Property of phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

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Technology Process of phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

There total 1 articles about phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-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:

: C₆₃H₇₂O₁₆S

: 1227637-18-4
phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

Guidance literature:: With methanol; potassium carbonate; for 1h; pH=9; Inert atmosphere;
DOI:10.1021/ja1009037

Reference yield: 76.0%

: 1227636-95-4
C₃₈H₅₀Cl₃NO₉Si

: 1227637-18-4
phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

: 1227636-94-3
phenyl [6-O-(tert-butyldimethylsilyl)-2,3,4-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->2)-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In diethyl ether; at 0 ℃; for 0.0833333h; Molecular sieve; Inert atmosphere;
DOI:10.1021/ja1009037

Reference yield: 72.0%

: 1227637-18-4
phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

: 1363902-76-4
C₄₂H₄₈Cl₃NO₉Si

: 1363902-83-3
phenyl [2-O-acetyl-6-O-(tert-butyldiphenylsilyl)-3,4-di-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->2)-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside

Guidance literature:: phenyl O-[3,4,6-tri-O-(p-methoxybenzyl)-α-D-mannopyranosyl]-(1->6)-2-O-allyl-3,4-di-O-(p-methoxybenzyl)-1-thio-α-D-mannopyranoside; C₄₂H₄₈Cl₃NO₉Si; In dichloromethane; at 20 ℃; for 1h; Inert atmosphere; Molecular sieve;

With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.166667h; stereoselective reaction; Inert atmosphere; Molecular sieve;
DOI:10.1002/chem.201102545