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7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate

Base Information
  • Chemical Name:7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate
  • CAS No.:642478-73-7
  • Molecular Formula:C39H31N4O9P
  • Molecular Weight:730.67
  • Hs Code.:
7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate

Synonyms:7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate

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Chemical Property of 7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate
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Technology Process of 7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate

There total 5 articles about 7-N-acetyldemethyllavendamycin β-hydroxyethyl ester dibenzyl phosphate 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 triphenylphosphine; diethylazodicarboxylate; In tetrahydrofuran; at 20 ℃; for 4 - 4.2h; Product distribution / selectivity;
Guidance literature:
Multi-step reaction with 3 steps
1: 87 percent / HCOONH4 / Pd/C / dimethylformamide / 4.5 h / 20 °C
2: 94 percent / methoxybenzene; dimethylformamide / 5.5 h / 95 - 160 °C
3: 142 mg / Ph3P; diethyl azodicarboxylate / tetrahydrofuran / 4 h / 20 °C
With ammonium formate; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; methoxybenzene; N,N-dimethyl-formamide; 2: Pictet-Spengler condensation / 3: Mitsunobu reaction;
DOI:10.1021/jm0304414
Guidance literature:
Multi-step reaction with 4 steps
1: 78 percent / Et3N / dibutyl ether / 5 h / Heating
2: 87 percent / HCOONH4 / Pd/C / dimethylformamide / 4.5 h / 20 °C
3: 94 percent / methoxybenzene; dimethylformamide / 5.5 h / 95 - 160 °C
4: 142 mg / Ph3P; diethyl azodicarboxylate / tetrahydrofuran / 4 h / 20 °C
With ammonium formate; triethylamine; triphenylphosphine; diethylazodicarboxylate; palladium on activated charcoal; In tetrahydrofuran; dibutyl ether; methoxybenzene; N,N-dimethyl-formamide; 3: Pictet-Spengler condensation / 4: Mitsunobu reaction;
DOI:10.1021/jm0304414
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