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(1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate

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  • Chemical Name:(1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate
  • CAS No.:925451-40-7
  • Molecular Formula:C47H62N2O6SSi
  • Molecular Weight:811.171
  • Hs Code.:
(1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl N<sup>α</sup>-benzoyl-N<sup>ε</sup>-(2''-trimethylsilyl)ethanesulfonyl-N<sup>ε</sup>-4'''-methoxybenzyl-L-α-vinyllysinate

Synonyms:(1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate

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Chemical Property of (1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate
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Technology Process of (1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate

There total 7 articles about (1R,2S)-trans-2-[2'-(β-naphthyl)-2'-propyl]cyclohexyl Nα-benzoyl-Nε-(2''-trimethylsilyl)ethanesulfonyl-Nε-4'''-methoxybenzyl-L-α-vinyllysinate 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:
2-benzoylamino-but-2-enoic acid 2-(1-methyl-1-naphthalen-2-yl-ethyl)-cyclohexyl ester; With n-butyllithium; lithium diisopropyl amide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; at -78 ℃;
N-(2'-trimethylsilyl)ethanesulfonyl-N-4''-iodobutyl-4-methoxybenzylamine; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; at -78 ℃; for 5h; Title compound not separated from byproducts;
DOI:10.1021/ja067240k
Guidance literature:
Multi-step reaction with 3 steps
1.1: n-butyllithium / tetrahydrofuran; hexane / 0.33 h / -78 °C
1.2: 77 percent / tetrahydrofuran; hexane / -78 - 20 °C
2.1: 91 percent / sodium iodide / acetone / 14 h / 50 °C / Heating
3.1: LDA; n-BuLi / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / -78 °C
3.2: tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 5 h / -78 °C
With n-butyllithium; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; acetone;
DOI:10.1021/ja067240k
Guidance literature:
Multi-step reaction with 2 steps
1.1: 91 percent / sodium iodide / acetone / 14 h / 50 °C / Heating
2.1: LDA; n-BuLi / tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / -78 °C
2.2: tetrahydrofuran; hexane; hexamethylphosphoric acid triamide / 5 h / -78 °C
With n-butyllithium; sodium iodide; lithium diisopropyl amide; In tetrahydrofuran; N,N,N,N,N,N-hexamethylphosphoric triamide; hexane; acetone;
DOI:10.1021/ja067240k
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