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(R)-diethyl 2-phenylsuccinate

Base Information
  • Chemical Name:(R)-diethyl 2-phenylsuccinate
  • CAS No.:1354896-76-6
  • Molecular Formula:C14H18O4
  • Molecular Weight:250.295
  • Hs Code.:
(R)-diethyl 2-phenylsuccinate

Synonyms:(R)-diethyl 2-phenylsuccinate

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Chemical Property of (R)-diethyl 2-phenylsuccinate
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Technology Process of (R)-diethyl 2-phenylsuccinate

There total 6 articles about (R)-diethyl 2-phenylsuccinate 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:
ethyl (R)-4-oxo-3-phenyl-4-(1-(o-tolyl)-1H-imidazol-2-yl)butanoate; With methyl trifluoromethanesulfonate; In acetonitrile; at 0 ℃; for 6h; Molecular sieve; Inert atmosphere;
ethanol; With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 0 ℃; for 1h; Molecular sieve; Inert atmosphere;
DOI:10.1021/jacs.6b07692
Guidance literature:
phenylboronic acid; With chlorobis(ethylene)rhodium(I) dimer; (S,S)-1,7,7-trimethyl-2,5-diphenylbicyclo[2.2.1]hepta-2,5-diene; potassium hydroxide; In methanol; dichloromethane; at 20 ℃; for 0.0833333h; Inert atmosphere;
diethyl Fumarate; In methanol; dichloromethane; isopropyl alcohol; at 60 ℃; for 1h; optical yield given as %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/ol300980k
Guidance literature:
With (S)-5-benzyl-2-mesityl-6,6-dimethyl-5,6-dihydro-8H-[1,2,4]triazolo[3,4-c][1,4]oxazin-2-ium tetrafluoroborate; 3,4-bis((3,5-bis(trifluoromethyl)phenyl)amino)cyclobut-3-ene-1,2-dione; N-ethyl-N,N-diisopropylamine; In water; 1,2-dichloro-ethane; at 0 ℃; for 48h; Reagent/catalyst; Temperature; Overall yield = 85 %; Overall yield = 41 mg; Optical yield = 88 %ee; enantioselective reaction; Inert atmosphere;
DOI:10.1021/jacs.5b02887
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