Ugi four-component condensation (Ugi-4CC) between 2-formylbenzoic acid, phenacylamine dimethyl acetal, and isocyanides afforded 1H-isochromen-1-ones (isocoumarins). These products, where structure corresponds to the tautomeric enediamine form of the Ugi-4CC primary adducts, were stable enough to allow their isolation and characterization. Stable isocoumarins were also obtained by employing anilines as the amino component in the Ugi four-component condensation.

Isolation of Ugi Four-Component Condensation Primary Adducts: A Straightforward Route to Isocoumarins / C.Faggi; M.Garcia-Valverde; S.Marcaccini; G.Menchi. - In: ORGANIC LETTERS. - ISSN 1523-7060. - STAMPA. - 12:(2010), pp. 788-791.

Isolation of Ugi Four-Component Condensation Primary Adducts: A Straightforward Route to Isocoumarins

FAGGI, CRISTINA;MARCACCINI, STEFANO;MENCHI, GLORIA
2010

Abstract

Ugi four-component condensation (Ugi-4CC) between 2-formylbenzoic acid, phenacylamine dimethyl acetal, and isocyanides afforded 1H-isochromen-1-ones (isocoumarins). These products, where structure corresponds to the tautomeric enediamine form of the Ugi-4CC primary adducts, were stable enough to allow their isolation and characterization. Stable isocoumarins were also obtained by employing anilines as the amino component in the Ugi four-component condensation.
2010
12
788
791
C.Faggi; M.Garcia-Valverde; S.Marcaccini; G.Menchi
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/385575
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