allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

Base Information

Chemical Name:allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside
CAS No.:743432-07-7
Molecular Formula:C₅₆H₄₈O₁₆
Molecular Weight:976.988
Hs Code.:

Synonyms:allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

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Chemical Property of allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

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Technology Process of allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

There total 1 articles about allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside 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: 87.2%

: 2,3-5-tri-O-benzoyl-α-D-arabinofuranosyl 2,2,2-trichloroacetimidate

: 578007-57-5
allyl-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

: 743432-07-7
allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

Guidance literature:: With trimethylsilyl trifluoromethanesulfonate; In dichloromethane; at -20 - 20 ℃;
DOI:10.1016/j.carres.2004.04.012

Reference yield:

: 743432-07-7
allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

: 743432-08-8
C₅₃H₄₄O₁₆

Guidance literature:: palladium dichloride; In methanol; at 20 ℃; for 2h;
DOI:10.1016/j.carres.2004.04.012

Reference yield:

: 743432-07-7
allyl 2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranoside

: 743432-09-9
2,3,5-tri-O-benzoyl-α-D-arabinofuranosyl-(1-> 2)-3,4,6-tri-O-benzoyl-α-D-mannopyranosyl trichloroacetimidate

Guidance literature:: Multi-step reaction with 2 steps

1: PdCl₂ / methanol / 2 h / 20 °C

2: 357 mg / DBU / CH₂Cl₂

With 1,8-diazabicyclo[5.4.0]undec-7-ene; palladium dichloride; In methanol; dichloromethane;
DOI:10.1016/j.carres.2004.04.012