isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

Base Information

Chemical Name:isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside
CAS No.:1269649-14-0
Molecular Formula:C₄₃H₄₈O₁₄S
Molecular Weight:820.912
Hs Code.:

Synonyms:isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

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Technology Process of isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

There total 1 articles about isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside 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: 92.0%

: 615570-26-8
isopropyl 3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

: 113893-72-4
2,3,4-tri-O-acetyl-L-rhamnopyranosyl trichloroacetimidate

: 1269649-14-0
isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at 0 ℃; for 0.75h; Inert atmosphere;
DOI:10.1016/j.bmcl.2010.12.046

Reference yield: 91.0%

: 1269649-14-0
isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

: 1269649-17-3
isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1016/j.bmcl.2010.12.046

Reference yield:

: 1269649-14-0
isopropyl 2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)-3-O-fluorenylmethoxycarbonyl-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

: 1269649-21-9
isopropyl 2,3,4-tri-O-benzoyl-β-D-xylopyranosyl-(1->3)-[2,3,4-tri-O-acetyl-α-L-rhamnopyranosyl-(1->2)]-4,6-di-O-benzylidene-1-thio-β-D-galactopyranoside

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 3 h / 20 °C

2: trimethylsilyl trifluoromethanesulfonate / dichloromethane / 0.75 h / 0 °C / Inert atmosphere

With trimethylsilyl trifluoromethanesulfonate; triethylamine; In dichloromethane;
DOI:10.1016/j.bmcl.2010.12.046