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N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester

Base Information
  • Chemical Name:N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester
  • CAS No.:1310360-92-9
  • Molecular Formula:C30H35NO4Si
  • Molecular Weight:501.698
  • Hs Code.:
N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester

Synonyms:N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester

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Chemical Property of N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester
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Technology Process of N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl ester

There total 3 articles about N-(2-(triphenylsilyl)ethoxy)carbonyl-L-leucine allyl 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:
Multi-step reaction with 3 steps
1.1: 9-bora-bicyclo[3.3.1]nonane / tetrahydrofuran / 3 h / Inert atmosphere; Reflux
1.2: 3 h / 45 °C / Inert atmosphere
2.1: pyridine / dichloromethane / 24 h / 20 °C / Inert atmosphere
3.1: triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere
With pyridine; triethylamine; 9-bora-bicyclo[3.3.1]nonane; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide;
DOI:10.3390/molecules16064695
Guidance literature:
Multi-step reaction with 2 steps
1: pyridine / dichloromethane / 24 h / 20 °C / Inert atmosphere
2: triethylamine / N,N-dimethyl-formamide / 24 h / 20 °C / Inert atmosphere
With pyridine; triethylamine; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.3390/molecules16064695
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