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C43H75NO11Si

Base Information
  • Chemical Name:C43H75NO11Si
  • CAS No.:922166-95-8
  • Molecular Formula:C43H75NO11Si
  • Molecular Weight:810.154
  • Hs Code.:
C<sub>43</sub>H<sub>75</sub>NO<sub>11</sub>Si

Synonyms:C43H75NO11Si

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Chemical Property of C43H75NO11Si
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Technology Process of C43H75NO11Si

There total 25 articles about C43H75NO11Si 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:
Guidance literature:
Multi-step reaction with 4 steps
1: 54 percent / n-BuLi / diethyl ether; hexane / 1.5 h / -78 °C
2: 100 percent / NaH / dimethylformamide / 0 - 20 °C
3: 97 percent / N,N-dimethylbarbituric acid; Pd(PPh3)4 / CH2Cl2 / 2.5 h / Heating
4: 75 percent / Et3N; N,N-dimethylaminopyridine / tetrahydrofuran / 6 h / Heating
With dmap; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; 1,3-dimethylbarbituric acid; sodium hydride; triethylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/ol062642i
Guidance literature:
Multi-step reaction with 19 steps
1.1: 4.37 mg / aq. HCl / tetrahydrofuran; CH2Cl2 / 3 h / 20 °C
2.1: 96 percent / (S,S)-chiral titanium complex / diethyl ether; tetrahydrofuran / 5 h / -78 °C
3.1: 97 percent / KH / tetrahydrofuran / 0 - 20 °C
4.1: 98 percent / [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh; N-allyl-N-tritylamine; diisopropylethylamine / toluene / 3.5 h / Heating
5.1: OsO4; H2O; N-methylmorpholine N-oxide / acetone / 16 h / 20 °C
6.1: aq. NaIO4 / acetone / 2.5 h / 20 °C
7.1: 2.73 g / 4 Angstroem molecular sieves / toluene / 2.5 h / -78 - 0 °C
8.1: 92 percent / KH / tetrahydrofuran / 0 - 20 °C
9.1: OsO4; H2O; N-methylmorpholine N-oxide / acetone / 18 h / 20 °C
10.1: aq. NaIO4 / acetone / 2.5 h / 20 °C
11.1: s-BuLi / tetrahydrofuran; cyclohexane / 4.5 h / -78 - -20 °C
11.2: 1.18 g / citric acid / tetrahydrofuran; cyclohexane; H2O / pH 4 - 5
12.1: BF3*Et2O / tetrahydrofuran; cyclohexane / -78 - -5 °C
12.2: 1.49 g / ethanolamine / pentane / 2.5 h / 0 °C
13.1: 94 percent / 2,6-lutidine / CH2Cl2 / 10 h / -78 °C
14.1: 82 percent / NH4F; MeOH / 9.5 h / Heating
15.1: Dess-Martin periodinane; NaHCO3 / CH2Cl2 / 4 h
16.1: 54 percent / n-BuLi / diethyl ether; hexane / 1.5 h / -78 °C
17.1: 100 percent / NaH / dimethylformamide / 0 - 20 °C
18.1: 97 percent / N,N-dimethylbarbituric acid; Pd(PPh3)4 / CH2Cl2 / 2.5 h / Heating
19.1: 75 percent / Et3N; N,N-dimethylaminopyridine / tetrahydrofuran / 6 h / Heating
With 2,6-dimethylpyridine; hydrogenchloride; methanol; dmap; ammonium fluoride; sodium periodate; osmium(VIII) oxide; tetrakis(triphenylphosphine) palladium(0); n-butyllithium; 1,3-dimethylbarbituric acid; (S,S)-chiral titanium; [1,3-Mes2-(N2C3H5)]Cl2(PCy3)Ru=CHPh; 4 A molecular sieve; boron trifluoride diethyl etherate; N-tritylprop-2-en-1-amine; water; sec.-butyllithium; potassium hydride; sodium hydride; sodium hydrogencarbonate; Dess-Martin periodane; 4-methylmorpholine N-oxide; triethylamine; N-ethyl-N,N-diisopropylamine; In tetrahydrofuran; diethyl ether; hexane; dichloromethane; cyclohexane; N,N-dimethyl-formamide; acetone; toluene; 11.1: Corey-Schlessinger olefination / 15.1: Dess-Martin oxidation;
DOI:10.1021/ol062642i
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