Technology Process of 2-(Trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(3,6-di-O-benzoyl-2-deoxy-β-D-lyxo-hexopyranosyl)-β-D-glucopyranoside
There total 12 articles about 2-(Trimethylsilyl)ethyl 2,3,6-tri-O-benzyl-4-O-(3,6-di-O-benzoyl-2-deoxy-β-D-lyxo-hexopyranosyl)-β-D-glucopyranoside which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 76 percent / N-iodosuccinimide / acetonitrile / 1.) 0 deg C, 1 h, 2.) r.t., 16 h
2: 97 percent / H2, Et3N / 10percent Pd/C / methanol; ethyl acetate / 1 h
3: 85 percent / 80percent aq. AcOH / 4.5 h / 50 °C
4: 1.) Bu2SnO / 1.) MeOH, reflux, 5 h, 2.) toluene, 4 deg C, 17 h; r.t., 0.5 h
With
N-iodo-succinimide; hydrogen; di(n-butyl)tin oxide; acetic acid; triethylamine;
palladium on activated charcoal;
In
methanol; ethyl acetate; acetonitrile;
DOI:10.1021/jo00127a042
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 99 percent / pyridine / CH2Cl2 / 2 h
2: 76 percent / N-iodosuccinimide / acetonitrile / 1.) 0 deg C, 1 h, 2.) r.t., 16 h
3: 97 percent / H2, Et3N / 10percent Pd/C / methanol; ethyl acetate / 1 h
4: 85 percent / 80percent aq. AcOH / 4.5 h / 50 °C
5: 1.) Bu2SnO / 1.) MeOH, reflux, 5 h, 2.) toluene, 4 deg C, 17 h; r.t., 0.5 h
With
pyridine; N-iodo-succinimide; hydrogen; di(n-butyl)tin oxide; acetic acid; triethylamine;
palladium on activated charcoal;
In
methanol; dichloromethane; ethyl acetate; acetonitrile;
DOI:10.1021/jo00127a042
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 76 percent / N-iodosuccinimide / acetonitrile / 1.) 0 deg C, 1 h, 2.) r.t., 16 h
2: 97 percent / H2, Et3N / 10percent Pd/C / methanol; ethyl acetate / 1 h
3: 85 percent / 80percent aq. AcOH / 4.5 h / 50 °C
4: 1.) Bu2SnO / 1.) MeOH, reflux, 5 h, 2.) toluene, 4 deg C, 17 h; r.t., 0.5 h
With
N-iodo-succinimide; hydrogen; di(n-butyl)tin oxide; acetic acid; triethylamine;
palladium on activated charcoal;
In
methanol; ethyl acetate; acetonitrile;
DOI:10.1021/jo00127a042