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dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside

Base Information Edit
  • Chemical Name:dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside
  • CAS No.:303069-75-2
  • Molecular Formula:C41H36FO11P
  • Molecular Weight:754.702
  • Hs Code.:
  • Mol file:303069-75-2.mol
dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside

Synonyms:dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside

Suppliers and Price of dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside
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Chemical Property of dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside Edit
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Technology Process of dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-galactopyranoside

There total 4 articles about dibenzylphosphoryl 2,3,4-tri-O-benzoyl-6-deoxy-6-fluoro-β-L-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:
Guidance literature:
1,2,3,4-tetra-O-benzoyl-6-deoxy-6-fluoro-L-galactopyranoside; With hydrogen bromide; acetic acid; In dichloromethane; at 20 ℃; for 3h;
phosphoric acid dibenzyl ester; With 3 Angstroem MS; silver carbonate; In diethyl ether; dichloromethane; acetonitrile; at 20 ℃; for 15h;
DOI:10.1016/S0968-0896(00)00139-5
Guidance literature:
Multi-step reaction with 2 steps
1.1: pyridine / 16 h / 20 °C
2.1: 30 percent HBr; AcOH / CH2Cl2 / 3 h / 20 °C
2.2: 75 percent / Ag2CO3; 3 Angstroem MS / CH2Cl2; diethyl ether; acetonitrile / 15 h / 20 °C
With hydrogen bromide; acetic acid; In pyridine; dichloromethane; 1.1: Acylation / 2.1: Bromination / 2.2: Substitution;
DOI:10.1016/S0968-0896(00)00139-5
Guidance literature:
Multi-step reaction with 4 steps
1.1: 77 percent / collidine; DAST / CH2Cl2 / 6 h / Heating
2.1: 68 percent / AcOH / H2O
3.1: pyridine / 16 h / 20 °C
4.1: 30 percent HBr; AcOH / CH2Cl2 / 3 h / 20 °C
4.2: 75 percent / Ag2CO3; 3 Angstroem MS / CH2Cl2; diethyl ether; acetonitrile / 15 h / 20 °C
With 2,3,5-trimethyl-pyridine; hydrogen bromide; acetic acid; 4,4'-diaminostilbene-2,2'-disulfonic acid; In pyridine; dichloromethane; water; 1.1: Fluorination / 2.1: Ring cleavage / 3.1: Acylation / 4.1: Bromination / 4.2: Substitution;
DOI:10.1016/S0968-0896(00)00139-5
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