Technology Process of methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate
There total 5 articles about methyl (2S,3S,4E)-3-(benzoylamino)-2-(benzoyloxy)-4-hexenoate which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 5 steps
1: 1.) n-BuLi, 3.) (+)-(camphorsulfonyloxaziridine / 1.) hexane, -78 deg C, 1 h, 2.) THF, -78 deg C, 1 h, 3.) -78 deg C, 6 h; warm to room temperature
2: 93 percent / Pd(PPh3)4, N,N'-dimethylbarbituric acid / CH2Cl2 / Ambient temperature
3: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
4: 98 percent formic acid / 3 h / 60 °C
5: SOCl2, Et3N / 2.5 h / Heating
With
tetrakis(triphenylphosphine) palladium(0); n-butyllithium; formic acid; thionyl chloride; 1,3-dimethylbarbituric acid; (1S)-(+)-(10-camphorsulfonyl)-oxaziridine; triethylamine;
In
tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)01051-5
- Guidance literature:
-
Multi-step reaction with 3 steps
1: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
2: 98 percent formic acid / 3 h / 60 °C
3: SOCl2, Et3N / 2.5 h / Heating
With
formic acid; thionyl chloride; triethylamine;
In
tetrahydrofuran;
DOI:10.1016/S0040-4020(98)01051-5
- Guidance literature:
-
Multi-step reaction with 4 steps
1: 93 percent / Pd(PPh3)4, N,N'-dimethylbarbituric acid / CH2Cl2 / Ambient temperature
2: 201 g / Et3N / tetrahydrofuran / 1.) room temperature, 1 h, 2.) reflux, overnight
3: 98 percent formic acid / 3 h / 60 °C
4: SOCl2, Et3N / 2.5 h / Heating
With
tetrakis(triphenylphosphine) palladium(0); formic acid; thionyl chloride; 1,3-dimethylbarbituric acid; triethylamine;
In
tetrahydrofuran; dichloromethane;
DOI:10.1016/S0040-4020(98)01051-5