2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

Base Information

Chemical Name:2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside
CAS No.:1256814-78-4
Molecular Formula:C₅₀H₄₄F₃NO₈
Molecular Weight:843.896
Hs Code.:

Synonyms:2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

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Chemical Property of 2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

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Technology Process of 2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

There total 1 articles about 2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside 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: 83.0%

: C₄₂H₄₀O₈

: 61881-19-4
2,2,2-trifluoro-N-phenyl-acetimidoyl chloride

: 1256814-78-4
2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

Guidance literature:: With potassium carbonate; In acetone; at 20 ℃; for 48h;
DOI:10.1021/jo101779v

Reference yield: 90.0%

: 1256814-79-5
methyl (phenyl 2-azido-3-O-benzyl-2-deoxy-1-thio-β-D-mannopyranosyl uronate)

: 1256814-78-4
2,3,4-tri-O-benzyl-6-O-(9-fluorenylmethoxycarbonyl)-1-O-(N-[phenyl]trifluoroacetimidoyl)-α-D-glucopyranoside

: 1256814-80-8
phenyl 4-O-[2,3,4-tri-O-benzyl-6-O-[9-fluorenylmethoxycarbonyl]-α-D-glucopyranosyl]-6-O-methyl-6-oxy-2-azido-3-O-benzyl-2-deoxy-1-thio-β-D-mannopyranoside

Guidance literature:: With trifluorormethanesulfonic acid; In diethyl ether; at -35 - -15 ℃; for 1.5h; diastereoselective reaction;
DOI:10.1021/jo101779v