Technology Process of C14H16O5
There total 4 articles about C14H16O5 which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
3,3-dimethyldioxirane;
In
dichloromethane;
at -55 ℃;
for 48h;
optical yield given as %de;
stereoselective reaction;
DOI:10.1021/jo102382r
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: sodium hydride / tetrahydrofuran; mineral oil / 0.75 h / 0 - 20 °C
1.2: 16 h / 20 °C
2.1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 0.5 h / Reflux
3.1: lithium 1-naphthalenide / tetrahydrofuran / -40 °C
4.1: 3,3-dimethyldioxirane / dichloromethane / 48 h / -55 °C
With
2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; 3,3-dimethyldioxirane; sodium hydride; lithium 1-naphthalenide;
In
tetrahydrofuran; dichloromethane; toluene; mineral oil;
DOI:10.1021/jo102382r
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride / toluene / 0.5 h / Reflux
2: lithium 1-naphthalenide / tetrahydrofuran / -40 °C
3: 3,3-dimethyldioxirane / dichloromethane / 48 h / -55 °C
With
2,2'-azobis(isobutyronitrile); tri-n-butyl-tin hydride; 3,3-dimethyldioxirane; lithium 1-naphthalenide;
In
tetrahydrofuran; dichloromethane; toluene;
DOI:10.1021/jo102382r