N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

Base Information

Chemical Name:N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester
CAS No.:117759-00-9
Molecular Formula:C₈₁H₈₀Cl₃N₃O₂₁
Molecular Weight:1537.89
Hs Code.:

N-(benzyloxycarbonyl)-L-alanyl-<O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl-(1->3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

Synonyms:N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

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Chemical Property of N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

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Technology Process of N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

There total 1 articles about N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester 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:

: 117747-53-2
N-(benzyloxycarbonyl)-L-alanyl-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

: 117758-95-9
O-(2,3,4,6-tetra-O-benzoyl-β-D-galactopyranosyl)-(1->3)-2,4,6-tri-O-benzyl-α-D-galactopyranosyl chloride

: 117759-00-9
N-(benzyloxycarbonyl)-L-alanyl-3)-O-(2,4,6-tri-O-benzyl-α-D-galactopyranosyl)-(1->3)>-L-threonyl-L-alanine 2,2,2-trichloroethyl ester

Guidance literature:: With 2,6-dimethylpyridine; calcium sulfate; tetramethylurea; silver trifluoromethanesulfonate; Yield given. Multistep reaction; 1.) CH₂Cl₂, 0 deg C, 2 h; 2.) CH₂Cl₂, 6 h, 25 deg C;
DOI:10.1016/0008-6215(88)85096-1