An improvement of a known two step cyclization procedure affording 4-aryl-3-hydroxy benzoic acid derivatives from 3-aryl-2,3-unsaturated aldehydes and dimethyl succinate is described. The high versatility of the synthetic procedure is shown as the aryl substituent can be a benzene or naphthalene moiety or an heteroaromatic ring. It can be applied iteratively to prepare p,p-oligophehyl derivatives. (C) 1997 Elsevier Science Ltd.
Brenna, Elizabetta; Fuganti, Claudio; Serra, Stefano, Journal of Chemical Research, Miniprint, 1998, # 2, p. 551 - 563
作者:Brenna, Elizabetta、Fuganti, Claudio、Serra, Stefano、Dulio, Andrea
DOI:——
日期:——
CLINCH, K.;MARQUEZ, C. J.;PARROTT, M. J.;RAMAGE, R., TETRAHEDRON, 45,(1989) N, C. 239-258
作者:CLINCH, K.、MARQUEZ, C. J.、PARROTT, M. J.、RAMAGE, R.