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7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>

Base Information
  • Chemical Name:7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>
  • CAS No.:160239-19-0
  • Molecular Formula:C59H85NO14Si2
  • Molecular Weight:1088.49
  • Hs Code.:
7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>

Synonyms:7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>

Suppliers and Price of 7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>
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Chemical Property of 7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>
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Technology Process of 7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate>

There total 4 articles about 7-O-(triethylsilyl)baccatrin III 13-O-<(2R,3S)-N-benzoyl-2-O-(tert-butyldimethylsilyl)-3-cyclohexylisoserinate> 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:
Multi-step reaction with 3 steps
1: 31 mg / H2 / 3percent Pt/C / ethyl acetate / 12 h / 2844.3 Torr
2: 96 percent / Et3N, DMAP / CH2Cl2 / 1 h / 0 °C
3: 71 percent / NaH / tetrahydrofuran / 1.5 h / 25 - 35 °C
With dmap; hydrogen; sodium hydride; triethylamine; platinum on activated charcoal; In tetrahydrofuran; dichloromethane; ethyl acetate;
DOI:10.1021/jm00046a018
Guidance literature:
Multi-step reaction with 2 steps
1: 96 percent / Et3N, DMAP / CH2Cl2 / 1 h / 0 °C
2: 71 percent / NaH / tetrahydrofuran / 1.5 h / 25 - 35 °C
With dmap; sodium hydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1021/jm00046a018
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