phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

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Chemical Name:phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside
CAS No.:1435738-66-1
Molecular Formula:C₅₀H₅₄O₅SSi₂
Molecular Weight:823.213
Hs Code.:

Synonyms:phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

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Chemical Property of phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

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Technology Process of phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

There total 1 articles about phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-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: 86.0%

: 1207338-44-0
phenyl 2-O-benzoyl-1-thio-α-D-arabinofuranoside

: 58479-61-1
tert-butylchlorodiphenylsilane

: 1435738-66-1
phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

Guidance literature:: phenyl 2-O-benzoyl-1-thio-α-D-arabinofuranoside; With 1H-imidazole; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;

tert-butylchlorodiphenylsilane; In N,N-dimethyl-formamide; at 0 - 20 ℃;
DOI:10.1021/ol401166x

Reference yield: 85.0%

: 1435738-66-1
phenyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-1-thio-α-D-arabinofuranoside

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

: 1435739-43-7
methyl 2-O-benzoyl-3,5-di-O-tert-butyldiphenylsilyl-α-D-arabinofuranosyl-(1→5)-2,3-di-Obenzoyl-α-D-arabinofuranoside

Guidance literature:: With N-iodo-succinimide; trifluorormethanesulfonic acid; In dichloromethane; at -80 - -60 ℃; for 1h; Molecular sieve;
DOI:10.1021/ol401166x