methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

Base Information

Chemical Name:methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside
CAS No.:352438-52-9
Molecular Formula:C₅₁H₄₆O₁₇
Molecular Weight:930.916
Hs Code.:

Synonyms:methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

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Chemical Property of methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

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Technology Process of methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

There total 7 articles about methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside 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: 89.0%

: 352438-51-8
methyl 5-O-[2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

: 352438-38-1
p-tolyl 2,3,5-tri-O-benzoyl-1-thio-α-D-arabinofuranoside

: 352438-52-9
methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

Guidance literature:: With N-iodo-succinimide; silver trifluoromethanesulfonate; In dichloromethane; at 0 ℃;
DOI:10.1021/jo001747a

Reference yield:

: 98-88-4
benzoyl chloride

: 352438-52-9
methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 2.52 g / pyridine / 0 - 20 °C

2: 84 percent / Ni-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.25 h / 0 °C

3: 81 percent / TBAF / tetrahydrofuran / 1 h / 0 °C

4: 89 percent / N-iodosuccinimide; silfer triflate / CH₂Cl₂ / 0 °C

With pyridine; N-iodo-succinimide; tetrabutyl ammonium fluoride; silver trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo001747a

Reference yield:

: 204918-55-8
p-cresyl 5-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

: 352438-52-9
methyl 5-O-[5-O-(2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl)-2,3-di-O-benzoyl-α-D-arabinofuranosyl]-2,3-anhydro-α-D-lyxofuranoside

Guidance literature:: Multi-step reaction with 4 steps

1: 2.52 g / pyridine / 0 - 20 °C

2: 84 percent / Ni-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.25 h / 0 °C

3: 81 percent / TBAF / tetrahydrofuran / 1 h / 0 °C

4: 89 percent / N-iodosuccinimide; silfer triflate / CH₂Cl₂ / 0 °C

With pyridine; N-iodo-succinimide; tetrabutyl ammonium fluoride; silver trifluoromethanesulfonate; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jo001747a