Technology Process of 1,3,5-tri-O-allyl-scyllo-inositol
There total 3 articles about 1,3,5-tri-O-allyl-scyllo-inositol which
guide to synthetic route it.
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synthetic route:
- Guidance literature:
-
Multi-step reaction with 3 steps
1.1: 100 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / 20 °C
2.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 °C
2.2: dimethylformamide / 2 h / 20 °C
3.1: 100 percent / p-toluene sulfonic acid / methanol; ethyl acetate / 1 h / 20 °C
With
sodium tetrahydroborate; sodium hydride; toluene-4-sulfonic acid;
In
tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1016/j.tetlet.2005.07.001
- Guidance literature:
-
Multi-step reaction with 2 steps
1.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 °C
1.2: dimethylformamide / 2 h / 20 °C
2.1: 100 percent / p-toluene sulfonic acid / methanol; ethyl acetate / 1 h / 20 °C
With
sodium hydride; toluene-4-sulfonic acid;
In
tetrahydrofuran; methanol; ethyl acetate;
DOI:10.1016/j.tetlet.2005.07.001
- Guidance literature:
-
Multi-step reaction with 4 steps
1.1: 78.5 percent / PCC; molecular sieve 4A / CH2Cl2 / 16 h / Heating
2.1: 100 percent / NaBH4 / methanol; tetrahydrofuran / 1 h / 20 °C
3.1: sodium hydride / tetrahydrofuran / 0.33 h / 0 °C
3.2: dimethylformamide / 2 h / 20 °C
4.1: 100 percent / p-toluene sulfonic acid / methanol; ethyl acetate / 1 h / 20 °C
With
sodium tetrahydroborate; 4 A molecular sieve; sodium hydride; toluene-4-sulfonic acid; pyridinium chlorochromate;
In
tetrahydrofuran; methanol; dichloromethane; ethyl acetate;
DOI:10.1016/j.tetlet.2005.07.001