Technology Process of C62H62N6O13S2
There total 8 articles about C62H62N6O13S2 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: lithium diisopropyl amide / tetrahydrofuran / 1 h / -70 °C
1.2: 1 h / -60 °C
1.3: -20 °C
2.1: sodium tetrahydroborate / ethanol / 0.5 h
3.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 0 °C
4.1: triethylamine tris(hydrogen fluoride) / tetrahydrofuran / 20 h / 23 °C
5.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.17 h / 0 °C
5.2: 1.5 h / 0 °C
6.1: dichloro-acetic acid; chlorotriisopropylsilane / dichloromethane / 0.75 h
7.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C
8.1: caesium carbonate; lithium bromide / N,N-dimethyl-formamide / 4 h
With
dichloro-acetic acid; dmap; sodium tetrahydroborate; chlorotriisopropylsilane; di-isopropyl azodicarboxylate; caesium carbonate; triethylamine tris(hydrogen fluoride); N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium bromide; lithium diisopropyl amide;
In
tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide;
5.1: Mitsunobu reaction / 5.2: Mitsunobu reaction;
DOI:10.1002/hlca.201000451
- Guidance literature:
-
Multi-step reaction with 6 steps
1.1: dmap; N-ethyl-N,N-diisopropylamine / dichloromethane / 4 h / 0 °C
2.1: triethylamine tris(hydrogen fluoride) / tetrahydrofuran / 20 h / 23 °C
3.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.17 h / 0 °C
3.2: 1.5 h / 0 °C
4.1: dichloro-acetic acid; chlorotriisopropylsilane / dichloromethane / 0.75 h
5.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C
6.1: caesium carbonate; lithium bromide / N,N-dimethyl-formamide / 4 h
With
dichloro-acetic acid; dmap; chlorotriisopropylsilane; di-isopropyl azodicarboxylate; caesium carbonate; triethylamine tris(hydrogen fluoride); N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium bromide;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
3.1: Mitsunobu reaction / 3.2: Mitsunobu reaction;
DOI:10.1002/hlca.201000451
- Guidance literature:
-
Multi-step reaction with 5 steps
1.1: triethylamine tris(hydrogen fluoride) / tetrahydrofuran / 20 h / 23 °C
2.1: di-isopropyl azodicarboxylate; triphenylphosphine / tetrahydrofuran / 0.17 h / 0 °C
2.2: 1.5 h / 0 °C
3.1: dichloro-acetic acid; chlorotriisopropylsilane / dichloromethane / 0.75 h
4.1: N-ethyl-N,N-diisopropylamine / dichloromethane / 2 h / 0 °C
5.1: caesium carbonate; lithium bromide / N,N-dimethyl-formamide / 4 h
With
dichloro-acetic acid; chlorotriisopropylsilane; di-isopropyl azodicarboxylate; caesium carbonate; triethylamine tris(hydrogen fluoride); N-ethyl-N,N-diisopropylamine; triphenylphosphine; lithium bromide;
In
tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
2.1: Mitsunobu reaction / 2.2: Mitsunobu reaction;
DOI:10.1002/hlca.201000451