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C33H32O12

Base Information Edit
C<sub>33</sub>H<sub>32</sub>O<sub>12</sub>

Synonyms:C33H32O12

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C33H32O12 Edit
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Technology Process of C33H32O12

There total 12 articles about C33H32O12 which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:
Guidance literature:
With trimethyltin(IV) hydroxide; In 1,2-dichloro-ethane; at 80 ℃; for 20h;
DOI:10.1021/ol302273r DOI:10.1021/ol302273r
Guidance literature:
Multi-step reaction with 3 steps
1: barium hydroxide monohydrate / methanol; tetrahydrofuran / 23 °C
2: palladium diacetate; (2S,3S)-N-acetyl-2-amino-3-methylpentanoic acid; potassium hydrogencarbonate; oxygen / tert-Amyl alcohol / 6 h / 85 °C
3: trimethyltin(IV) hydroxide / 1,2-dichloro-ethane / 20 h / 80 °C
With barium hydroxide monohydrate; (2S,3S)-N-acetyl-2-amino-3-methylpentanoic acid; oxygen; palladium diacetate; potassium hydrogencarbonate; trimethyltin(IV) hydroxide; In tetrahydrofuran; methanol; tert-Amyl alcohol; 1,2-dichloro-ethane;
DOI:10.1021/ol302273r DOI:10.1021/ol302273r
Guidance literature:
Multi-step reaction with 3 steps
1: triethylamine; dmap / dichloromethane / 49 h / 0 - 23 °C
2: palladium diacetate; (2S,3S)-N-acetyl-2-amino-3-methylpentanoic acid; potassium hydrogencarbonate; oxygen / tert-Amyl alcohol / 6 h / 85 °C
3: trimethyltin(IV) hydroxide / 1,2-dichloro-ethane / 20 h / 80 °C
With dmap; (2S,3S)-N-acetyl-2-amino-3-methylpentanoic acid; oxygen; palladium diacetate; potassium hydrogencarbonate; triethylamine; trimethyltin(IV) hydroxide; In tert-Amyl alcohol; dichloromethane; 1,2-dichloro-ethane;
DOI:10.1021/ol302273r DOI:10.1021/ol302273r
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