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RESEARCH PRODUCT
ChemInform Abstract: Modular One-Pot Synthesis of Tetrasubstituted Pyrroles from α-(Alkylideneamino)nitriles.
Ines BergnerTill Opatzsubject
chemistry.chemical_compoundchemistryOne-pot synthesisOrganic chemistryRegioselectivityNitroalkaneGeneral MedicineRing (chemistry)Combinatorial chemistryCycloadditionPyrrole derivativesPyrroledescription
2,3,4,5-Tetrasubstituted pyrroles have been prepared with high regioselectivity by a formal cycloaddition of α-(alkylideneamino)nitriles and nitroolefins followed by elimination of HCN and HNO2. The reaction allows the convergent construction of the pyrrole ring in four steps from a nitroalkane and three aldehydes.
year | journal | country | edition | language |
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2008-01-29 | ChemInform |