2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

Base Information

Chemical Name:2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate
CAS No.:1240486-86-5
Molecular Formula:C₃₄H₄₀Cl₃NO₇Si
Molecular Weight:709.139
Hs Code.:

Synonyms:2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

Suppliers and Price of 2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

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 2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of 2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

There total 1 articles about 2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate 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:

: C₃₂H₄₀O₇Si

: 545-06-2
trichloroacetonitrile

: 1240486-86-5
2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In dichloromethane; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1021/jo101231r

Reference yield: 85.0%

: 1240486-86-5
2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate

: 1240486-94-5
1-(methoxycarbonyl)pentadec-10(S)-yl 3,4,6-tri-O-p-methoxybenzyl-β-D-glucopyranoside

: 1240486-95-6
1-(methoxycarbonyl)pentadec-10(S)-yl 2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl-(1->2)-3,4,6-tri-O-p-methoxybenzyl-β-D-glucopyranoside

Guidance literature:: 1-(methoxycarbonyl)pentadec-10(S)-yl 3,4,6-tri-O-p-methoxybenzyl-β-D-glucopyranoside; With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -78 ℃; for 0.0833333h; Molecular sieve; Inert atmosphere;

2-O-acetyl-3-O-p-methoxybenzyl-4-O-tert-butyldiphenylsilyl-α-L-rhamnopyranosyl trichloroacetimidate; In dichloromethane; at -78 - 0 ℃; stereoselective reaction; Inert atmosphere;
DOI:10.1021/jo101231r