methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

Base Information

Chemical Name:methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside
CAS No.:402759-03-9
Molecular Formula:C₃₂H₃₈O₉
Molecular Weight:566.648
Hs Code.:

Synonyms:methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

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Chemical Property of methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

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Technology Process of methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

There total 9 articles about methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside 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: 84.0%

: 20194-18-7
sodium phenyl-methanolate

: 527681-84-1
methyl 5-O-(2,3-anhydro-5-O-benzoyl-α-D-ribofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

: 402759-03-9
methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: In benzyl alcohol; at 120 ℃; for 3h;
DOI:10.1021/ja029302m

Reference yield:

: ((1R,2R,5R)-4-p-Tolylsulfanyl-3,6-dioxa-bicyclo[3.1.0]hex-2-yl)-methanol

: 402759-03-9
methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 3 steps

1: 1.21 g / pyridine / 2 h / 0 - 20 °C

2: 82 percent / 4 A molecular sieves; N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.17 h / -40 °C

3: 84 percent / phenylmethanol / 3 h / 120 °C

With pyridine; N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; benzyl alcohol;
DOI:10.1021/ja029302m

Reference yield:

: 527680-93-9
p-tolyl 2,3-anhydro-5-O-benzoyl-1-thio-β-D-ribofuranoside

: 402759-03-9
methyl 5-O-(2-O-benzyl-α-D-arabinofuranosyl)-2,3-di-O-benzyl-α-D-arabinofuranoside

Guidance literature:: Multi-step reaction with 2 steps

1: 82 percent / 4 A molecular sieves; N-iodosuccinimide; silver triflate / CH₂Cl₂ / 0.17 h / -40 °C

2: 84 percent / phenylmethanol / 3 h / 120 °C

With N-iodo-succinimide; 4 A molecular sieve; silver trifluoromethanesulfonate; In dichloromethane; benzyl alcohol;
DOI:10.1021/ja029302m