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(2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate

Base Information
  • Chemical Name:(2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate
  • CAS No.:1192350-63-2
  • Molecular Formula:C42H53NO7S
  • Molecular Weight:715.951
  • Hs Code.:
(2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate

Synonyms:(2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate

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Chemical Property of (2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate
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Technology Process of (2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate

There total 5 articles about (2R,3R,5S,6S)-((1R,2S)-2-(N-benzyl-2,4,6-trimethylphenylsulfonamido)-1-phenylpropyl) 3-hydroxy-6-(4-methoxybenzyloxy)-2,5-dimethylheptanoate 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:
(1R,2S)-2-(N-benzyl-N-mesitylenesulfonyl)amino-1-phenyl-1-propyl propionate; With triethylamine; dicyclohexyl(((trifluoromethyl)sulfonyl)oxy)borane; In hexane; dichloromethane; at -78 ℃; for 3h;
(3S,4S)-4-(4-methoxybenzyloxy)-3-methylpentanal; In hexane; dichloromethane; at -78 - 23 ℃; for 3h;
With water; dihydrogen peroxide; In methanol;
DOI:10.1021/ol902110a
Guidance literature:
Multi-step reaction with 4 steps
1.1: dmap; triethylamine / dichloromethane / 0 - 20 °C
2.1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 3 h / 0 - 23 °C
3.1: ozone / dichloromethane / -78 °C
3.2: -78 - 20 °C
4.1: triethylamine; dicyclohexyl(((trifluoromethyl)sulfonyl)oxy)borane / dichloromethane / 3 h / -78 °C
4.2: 3 h / -78 - 20 °C
4.3: 20 °C
With dmap; lithium aluminium tetrahydride; ozone; triethylamine; dicyclohexyl(((trifluoromethyl)sulfonyl)oxy)borane; In tetrahydrofuran; diethyl ether; dichloromethane; 4.1: Aldol reaction / 4.2: Aldol reaction;
DOI:10.1016/j.tet.2011.07.066
Guidance literature:
Multi-step reaction with 3 steps
1.1: lithium aluminium tetrahydride / tetrahydrofuran; diethyl ether / 3 h / 0 - 23 °C
2.1: ozone / dichloromethane / -78 °C
2.2: -78 - 20 °C
3.1: triethylamine; dicyclohexyl(((trifluoromethyl)sulfonyl)oxy)borane / dichloromethane / 3 h / -78 °C
3.2: 3 h / -78 - 20 °C
3.3: 20 °C
With lithium aluminium tetrahydride; ozone; triethylamine; dicyclohexyl(((trifluoromethyl)sulfonyl)oxy)borane; In tetrahydrofuran; diethyl ether; dichloromethane; 3.1: Aldol reaction / 3.2: Aldol reaction;
DOI:10.1016/j.tet.2011.07.066
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