methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

Base Information

Chemical Name:methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside
CAS No.:1435740-55-8
Molecular Formula:C₇₈H₈₀O₂₄Si
Molecular Weight:1429.56
Hs Code.:

methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

Synonyms:methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

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Chemical Property of methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

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Technology Process of methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

There total 1 articles about methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-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: 91.0%

: 1207338-43-9
phenyl 2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-1-thio-α-D-arabinofuranoside

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phenyl 2,5-di-O-benzoyl-1-thio-α-D-arabinofuranoside

: 204918-51-4
methyl 2,3-di-O-benzoyl-α-D-arabinofuranoside

: 1435740-49-0
methyl 2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-Obenzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

: 1435740-55-8
methyl2-O-benzoyl-3,5-O-(di-tert-butylsilylene)-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→3)-2,5-di-O-benzoyl-α-D-arabinofuranosyl-(1→5)-2,3-di-O-benzoyl-α-D-arabinofuranoside

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; at -80 - 0 ℃; for 2h; Molecular sieve;
DOI:10.1021/ol401166x