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N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester

Base Information
  • Chemical Name:N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester
  • CAS No.:76398-77-1
  • Molecular Formula:C24H28N2O7
  • Molecular Weight:456.496
  • Hs Code.:
N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester
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Technology Process of N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester

There total 1 articles about N-(t-butoxycarbonyl)-O-benzyl-L-serine N-hydroxy-5-norbornene-2,3-dicarboximide ester 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 dicyclohexyl-carbodiimide; In N,N-dimethyl-formamide; acetonitrile; 1.) 0 deg C, 1 h, 2.) RT, 4 h;
DOI:10.1246/bcsj.53.2570
Guidance literature:
Multi-step reaction with 2 steps
1: acetonitrile / 15 h / Ambient temperature
2: CF3COOH / 0.33 h / Ambient temperature
With trifluoroacetic acid; In acetonitrile;
DOI:10.1246/bcsj.53.2570
Guidance literature:
Multi-step reaction with 3 steps
1: acetonitrile / 15 h / Ambient temperature
2: CF3COOH / 0.33 h / Ambient temperature
3: acetonitrile / 15 h / Ambient temperature
With trifluoroacetic acid; In acetonitrile;
DOI:10.1246/bcsj.53.2570
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