Technology Process of C43H66O8S2Si
There total 18 articles about C43H66O8S2Si which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
trimethylsilyl trifluoromethanesulfonate;
In
dichloromethane;
at -78 - -40 ℃;
DOI:10.1016/j.bmcl.2006.09.004
- Guidance literature:
-
Multi-step reaction with 8 steps
1.1: EDC*HCl; DMAP; CSA / CH2Cl2 / Heating
2.1: H2O; TsOH / methanol / 20 °C
3.1: 2,6-lutidine / dimethylformamide / 0 °C
4.1: Cp2Ti[P(OEt)3]2 / tetrahydrofuran / 20 °C
5.1: BH3*THF / 0 - 20 °C
5.2: NaBO3 / H2O; tetrahydrofuran / Heating
6.1: 93 percent / Dess-Martin periodinane / CH2Cl2 / 20 °C
7.1: 63 percent / DDQ / H2O; CH2Cl2 / 0 - 20 °C
8.1: 87 percent / TMSOTf / CH2Cl2 / -78 - -40 °C
With
2,6-dimethylpyridine; dmap; borane-THF; titanocene(II) triethylphosphite complex; trimethylsilyl trifluoromethanesulfonate; camphor-10-sulfonic acid; water; Dess-Martin periodane; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.09.004
- Guidance literature:
-
Multi-step reaction with 9 steps
1.1: 97 percent / KOH / methanol; tetrahydrofuran; H2O / Heating
2.1: EDC*HCl; DMAP; CSA / CH2Cl2 / Heating
3.1: H2O; TsOH / methanol / 20 °C
4.1: 2,6-lutidine / dimethylformamide / 0 °C
5.1: Cp2Ti[P(OEt)3]2 / tetrahydrofuran / 20 °C
6.1: BH3*THF / 0 - 20 °C
6.2: NaBO3 / H2O; tetrahydrofuran / Heating
7.1: 93 percent / Dess-Martin periodinane / CH2Cl2 / 20 °C
8.1: 63 percent / DDQ / H2O; CH2Cl2 / 0 - 20 °C
9.1: 87 percent / TMSOTf / CH2Cl2 / -78 - -40 °C
With
2,6-dimethylpyridine; dmap; potassium hydroxide; borane-THF; titanocene(II) triethylphosphite complex; trimethylsilyl trifluoromethanesulfonate; camphor-10-sulfonic acid; water; Dess-Martin periodane; toluene-4-sulfonic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; 2,3-dicyano-5,6-dichloro-p-benzoquinone;
In
tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2006.09.004