Technology Process of C21H16BrNO
There total 4 articles about C21H16BrNO which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
With
3BF4(1-)*C36H58BrN4(3+); (Ra)-4-hydroxy-2,6-bis(2,4,6-triisopropylphenyl)-9,14-bis(triisopropylsilyl)dinaphtho[1,3,2]dioxaphosphepine 4-oxide; sodium phosphate;
In
hexane; para-xylene;
at 20 ℃;
for 4h;
optical yield given as %ee;
enantioselective reaction;
Inert atmosphere;
DOI:10.1021/ja305795x
- Guidance literature:
-
With
1,3-dibromo-5,5-dimethylimidazolidine-2,4-dione; C40H39N3O2;
In
methanol;
at -80 ℃;
for 6h;
Reagent/catalyst;
Overall yield = 93 percent; enantioselective reaction;
DOI:10.1021/acs.joc.9b02395
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: sodium t-butanolate / diethyl ether / 0.5 h / 0 °C / Inert atmosphere
1.2: Reflux; Inert atmosphere
2.1: triethylamine / dichloromethane / 0.5 h / Inert atmosphere
3.1: 3BF4(1-)*C36H58BrN4(3+); (Ra)-4-hydroxy-2,6-bis(2,4,6-triisopropylphenyl)-9,14-bis(triisopropylsilyl)dinaphtho[1,3,2]dioxaphosphepine 4-oxide; sodium phosphate / hexane; para-xylene / 4 h / 20 °C / Inert atmosphere
With
3BF4(1-)*C36H58BrN4(3+); (Ra)-4-hydroxy-2,6-bis(2,4,6-triisopropylphenyl)-9,14-bis(triisopropylsilyl)dinaphtho[1,3,2]dioxaphosphepine 4-oxide; triethylamine; sodium phosphate; sodium t-butanolate;
In
diethyl ether; hexane; dichloromethane; para-xylene;
1.2: Wittig reaction;
DOI:10.1021/ja305795x