Technology Process of C24H32O5S
There total 8 articles about C24H32O5S which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
dimethylsulfide borane complex; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole;
In
tetrahydrofuran;
at 0 - 6 ℃;
for 0.333333h;
optical yield given as %ee;
DOI:10.1021/ja804659n
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 88 percent / Grubbs-Hoveyda catalyst / CH2Cl2 / 40 °C
2.1: n-BuLi / diethyl ether / -78 °C
2.2: MgBr2*OEt2 / diethyl ether / -78 - 0 °C
2.3: THF / diethyl ether / 20 °C
3.1: 4-dimethylaminopyridine; pyridine / CH2Cl2
4.1: (S)-1-Me-3,3-diPh-tetrahydropyrrolo[1,2-c][1,3,2]oxazaborole; BH3*SMe2 / tetrahydrofuran / 0 °C
With
pyridine; dmap; n-butyllithium; dimethylsulfide borane complex; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole;
[1,3-bis-(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(O-isopropoxyphenylmethylene)ruthenium;
In
tetrahydrofuran; diethyl ether; dichloromethane;
4.1: Corey-Bakshi-Shibata reduction;
DOI:10.1002/anie.200701515
- Guidance literature:
-
With
dimethylsulfide borane complex; (S)-1-methyl-3,3-diphenyl-hexahydropyrrolo[1,2-c][1,3,2]oxazaborole;
In
tetrahydrofuran;
at 0 ℃;
Title compound not separated from byproducts.;
DOI:10.1002/anie.200701515