Technology Process of (Z)-7-(phenylsulfonyl)-2,7,8-nonatrien-1-ol
There total 9 articles about (Z)-7-(phenylsulfonyl)-2,7,8-nonatrien-1-ol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
hydrogenchloride;
In
methanol;
at 20 ℃;
DOI:10.1021/jo0488614
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: NaBH4; aq. NaOH; H2 / Ni(OAc)2*4H2O; ethylenediamine / ethanol / 1 h / 20 °C
2.1: imidazole / dimethylformamide / 2 h / 20 °C
3.1: 227 mg / PPTS / methanol; tetrahydrofuran / 20 °C
4.1: 100 percent / PPh3; imidazole; I2 / CH2Cl2 / 0 - 20 °C
5.1: n-BuLi / tetrahydrofuran; hexane; various solvent(s) / 1 h / -78 °C
5.2: hexane; tetrahydrofuran; various solvent(s) / -78 - 20 °C
6.1: 306 mg / PPTS / methanol; tetrahydrofuran / 20 °C
7.1: Et3N / tetrahydrofuran / -78 °C
8.1: H2O2; (NH4)6Mo7O24*4H2O / ethanol / 0 °C
9.1: aq. HCl / methanol / 20 °C
With
1H-imidazole; hydrogenchloride; ammonium heptamolybdate; sodium hydroxide; sodium tetrahydroborate; n-butyllithium; hydrogen; dihydrogen peroxide; iodine; pyridinium p-toluenesulfonate; triethylamine; triphenylphosphine;
nickel diacetate; ethylenediamine;
In
tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0488614
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: imidazole / dimethylformamide / 2 h / 20 °C
2.1: 227 mg / PPTS / methanol; tetrahydrofuran / 20 °C
3.1: 100 percent / PPh3; imidazole; I2 / CH2Cl2 / 0 - 20 °C
4.1: n-BuLi / tetrahydrofuran; hexane; various solvent(s) / 1 h / -78 °C
4.2: hexane; tetrahydrofuran; various solvent(s) / -78 - 20 °C
5.1: 306 mg / PPTS / methanol; tetrahydrofuran / 20 °C
6.1: Et3N / tetrahydrofuran / -78 °C
7.1: H2O2; (NH4)6Mo7O24*4H2O / ethanol / 0 °C
8.1: aq. HCl / methanol / 20 °C
With
1H-imidazole; hydrogenchloride; ammonium heptamolybdate; n-butyllithium; dihydrogen peroxide; iodine; pyridinium p-toluenesulfonate; triethylamine; triphenylphosphine;
In
tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo0488614