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O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester

Base Information
  • Chemical Name:O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester
  • CAS No.:1067639-83-1
  • Molecular Formula:C21H20N2O7
  • Molecular Weight:412.399
  • Hs Code.:
O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester

Synonyms:O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester

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Chemical Property of O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester
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Technology Process of O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester

There total 1 articles about O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl 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:
N-hydroxyphthalimide; With 1,8-diazabicyclo[5.4.0]undec-7-ene; In N,N-dimethyl-formamide; at 0 ℃; for 0.5h;
(S )-methyl 2-(((benzyloxy)carbonyl)amino)-4-((methylsulfonyl)oxy)butanoate; In N,N-dimethyl-formamide; at 20 ℃; for 48h;
DOI:10.1055/s-2008-1078600
Guidance literature:
O-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-N-[(phenylmethoxy)carbonyl]-L-homoserine methyl ester; With methylhydrazine; In dichloromethane; at 0 - 20 ℃; for 2h; Inert atmosphere;
N,N'-bis( tert-butoxycarbonyl)-1H-pyrazole-1-carboxamidine; With triethylamine; In tetrahydrofuran; Inert atmosphere;
DOI:10.1021/acsmedchemlett.5b00336
Guidance literature:
With methylhydrazine; In dichloromethane; at 0 ℃; for 1h;
DOI:10.1055/s-2008-1078600
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