ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

Base Information

Chemical Name:ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside
CAS No.:1240408-08-5
Molecular Formula:C₄₇H₅₂O₇SSi
Molecular Weight:789.077
Hs Code.:

Synonyms:ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

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Chemical Property of ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

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Technology Process of ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

There total 1 articles about ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-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:

: C₃₃H₄₄O₅SSi

: 98-88-4
benzoyl chloride

: 1240408-08-5
ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

Guidance literature:: With pyridine; at 50 ℃; for 16h;
DOI:10.1016/j.carres.2009.11.012

Reference yield: 73.0%

: 14218-11-2,14218-30-5,61198-88-7,108438-33-1,108836-02-8,114682-36-9,127305-34-4,151377-77-4
2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide

: 1240408-08-5
ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside

: 1240408-09-6
ethyl 2,3,4,6-tetra-O-benzoyl-α-D-mannopyranosyl-(1->6)-2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-α-D-mannopyranoside

Guidance literature:: 2,3,4,6-Tetra-O-benzoyl-α-D-mannopyranosyl bromide; ethyl 2,4-di-O-benzoyl-3-O-(tert-butyldimethylsilyl)-1-thio-6-O-trityl-α-D-mannopyranoside; In dichloromethane; at 20 ℃; for 0.5h; Molecular sieve;

With silver trifluoromethanesulfonate; In dichloromethane; at -20 - -10 ℃;
DOI:10.1016/j.carres.2009.11.012