phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

Base Information

Chemical Name:phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide
CAS No.:1083236-92-3
Molecular Formula:C₃₁H₃₄O₈S
Molecular Weight:566.672
Hs Code.:

Synonyms:phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

Suppliers and Price of phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

There total 1 articles about phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide 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: 90.0%

: 1083236-91-2
phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside

: 1083236-92-3
phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at -78 - -30 ℃; for 0.666667h; Inert atmosphere;
DOI:10.1021/jo801630m

Reference yield: 75.0%

: 1083236-92-3
phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide

: 108-93-0
cyclohexanol

: 1083236-93-4
cyclohexyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-α-D-mannopyranoside

Guidance literature:: phenyl 3-O-tert-butoxycarbonyl-2-O-benzyl-4,6-O-benzylidene-1-thio-α-D-mannopyranoside S-oxide; With trifluoromethylsulfonic anhydride; 2,4,5-tri-tert-butylpyrimidine; In dichloromethane; at -60 ℃; Inert atmosphere;

cyclohexanol; In dichloromethane; at -60 ℃; Inert atmosphere;
DOI:10.1021/jo801630m