6533b838fe1ef96bd12a46ab
RESEARCH PRODUCT
A green way to gamma-lactams through a copper catalyzed ARGET-ATRC in ethanol and in the presence of ascorbic acid
Fulvia FellugaDomenico SpinelliVincenzo FrennaRoberto CasolariUgo Maria PagnoniFranco GhelfiAndrew F. Parsonssubject
EthanolOrganic ChemistrySubstrate (chemistry)Settore CHIM/06 - Chimica OrganicaAscorbic acidHalocompoundsATRCg-LactamsCuClAscorbic acidBiochemistryMedicinal chemistryradical cyclizationCatalysisSolventchemistry.chemical_compoundCatalytic cyclechemistrylactamDrug DiscoveryOrganic chemistryascorbic acidlactam; ascorbic acid; radical cyclizationIsomerizationHalocompounds; ATRC; gamma-lactams; CuCl; ascorbic acid.Stoichiometrydescription
Abstract A ‘green’ ARGET-ATRC, for the CuCl[PMDETA] catalysed cyclo -isomerization of N -allyl-α-polychloroamides to γ-lactams is described. The process works efficiently (yields 78–96%), uses a bio-solvent, as ethanol, and exploits the reducing feature of ascorbic acid to limit, at a low level (2–4%), the amount of catalyst. To preserve the efficacy of the catalytic cycle, addition of Na 2 CO 3 is essential, which quenches the HCl released during the CuCl[PMDETA] regeneration step. Profitable features of the process are: mild reaction temperatures (25–37 °C), relatively short reaction times (usually 5 h) and low solvent volumes (2 mmol of substrate/mL of ethanol). The method, upon stoichiometric adjustment, was also used for the synthesis of α,β-unsaturated-γ-lactams from N -(2-chloroallyl)-α-polychloroamides, via a tandem process involving an ATRC and a reductive [1,2]-elimination.
year | journal | country | edition | language |
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2011-01-01 |