Technology Process of (SS,RR)-monocyclofarnesal N-methylnitrone
There total 5 articles about (SS,RR)-monocyclofarnesal N-methylnitrone which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
sodium methylate;
In
ethanol;
at 25 ℃;
for 18h;
DOI:10.1021/jo00209a003
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 68 percent / water, NBS / tetrahydrofuran / 4 h / 25 °C
2: 85percent phosphoric acid / hexane / 6 h / 25 °C
3: 1.) zinc, glacial AcOH, 2.) LiAlH4 / 1.) ether, reflux, 18 h, 2.) THF, reflux, 17 h
4: 81 percent / pyridine, CrO3 / CH2Cl2 / 1.5 h / 25 °C
5: 76 percent / sodium methoxide / ethanol / 18 h / 25 °C
With
pyridine; chromium(VI) oxide; N-Bromosuccinimide; lithium aluminium tetrahydride; phosphoric acid; water; sodium methylate; acetic acid; zinc;
In
tetrahydrofuran; ethanol; hexane; dichloromethane;
DOI:10.1021/jo00209a003
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 85percent phosphoric acid / hexane / 6 h / 25 °C
2: 1.) zinc, glacial AcOH, 2.) LiAlH4 / 1.) ether, reflux, 18 h, 2.) THF, reflux, 17 h
3: 81 percent / pyridine, CrO3 / CH2Cl2 / 1.5 h / 25 °C
4: 76 percent / sodium methoxide / ethanol / 18 h / 25 °C
With
pyridine; chromium(VI) oxide; lithium aluminium tetrahydride; phosphoric acid; sodium methylate; acetic acid; zinc;
In
ethanol; hexane; dichloromethane;
DOI:10.1021/jo00209a003