Technology Process of C34H59N3O5Si
There total 17 articles about C34H59N3O5Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
tetrabutyl ammonium fluoride; acetic acid;
In
tetrahydrofuran;
for 1h;
DOI:10.1002/anie.200603353
- Guidance literature:
-
Multi-step reaction with 10 steps
1.1: 89 percent / DIBAL-H / CH2Cl2 / 2 h
2.1: Et3N; (cyclohexyl)2BOTf / CH2Cl2; hexane / 2.33 h
2.2: 86 percent / CH2Cl2 / 14 h / cooling
3.1: 17.1 mmol / NaH / various solvent(s) / 0.42 h
4.1: 75 percent / 2,6-lutidine / CH2Cl2 / 0.58 h
5.1: 98 percent / ceric ammonium nitrate / acetonitrile; H2O / 1 h
6.1: 86 percent / 2,6-lutidine / CH2Cl2 / 0.5 h
7.1: 59 percent / diisobutylaluminium hydride / CH2Cl2 / -78 - 20 °C
8.1: 80 percent / Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 20 °C
9.1: 94 percent / LDA / hexane; tetrahydrofuran / 0.25 h / cooling
10.1: 99 percent / tetra-n-butylammonium fluoride; acetic acid / tetrahydrofuran / 1 h
With
2,6-dimethylpyridine; ammonium cerium(IV) nitrate; tetrabutyl ammonium fluoride; sodium hydride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; acetic acid; triethylamine; lithium diisopropyl amide;
In
tetrahydrofuran; hexane; dichloromethane; water; acetonitrile;
DOI:10.1002/anie.200603353
- Guidance literature:
-
Multi-step reaction with 7 steps
1: 75 percent / 2,6-lutidine / CH2Cl2 / 0.58 h
2: 98 percent / ceric ammonium nitrate / acetonitrile; H2O / 1 h
3: 86 percent / 2,6-lutidine / CH2Cl2 / 0.5 h
4: 59 percent / diisobutylaluminium hydride / CH2Cl2 / -78 - 20 °C
5: 80 percent / Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 1 h / 20 °C
6: 94 percent / LDA / hexane; tetrahydrofuran / 0.25 h / cooling
7: 99 percent / tetra-n-butylammonium fluoride; acetic acid / tetrahydrofuran / 1 h
With
2,6-dimethylpyridine; ammonium cerium(IV) nitrate; tetrabutyl ammonium fluoride; diisobutylaluminium hydride; sodium hydrogencarbonate; Dess-Martin periodane; acetic acid; lithium diisopropyl amide;
In
tetrahydrofuran; hexane; dichloromethane; water; acetonitrile;
DOI:10.1002/anie.200603353