Domino syntheses of five-, six- and seven-membered O-, N- and S-heterocycles from α-, β- and γ-substituted carboxylic esters
作者:J. Löffler、R. Schobert
DOI:10.1039/p19960002799
日期:——
By a one-pot procedure, tetronic acids, tetronates, coumarins, benzoxepinones and their N- and S-analogues are readily accessible from keteneylidene(triphenyl)phosphorane 2 and carboxylic esters bearing OH, NHR or SH groups in an alpha-, beta- or gamma-position by an addition/Wittig olefination/(Claisen rearrangement) sequence. This cascade can be controlled by temperature variation. Extension of this procedure by a further addition step yielding annulated bisheterocycles such as the furoquinolone 28 is possible in some cases.
BESTMANN, H. J.;SCHMID, G.;SANDMEIER, D.;SCHADE, G.;OECHSNER, H., CHEM. BER., 1985, 118, N 4, 1709-1719
作者:BESTMANN, H. J.、SCHMID, G.、SANDMEIER, D.、SCHADE, G.、OECHSNER, H.