Reactions of beta-chloro-alpha-cyano-beta-(5-nitrofur-2-yl)-acrylic acid derivatives with malonic acid derivatives in the presence of collidine yield the allyl anions 3 a-d. The pyridines 4, 8 or 9 are formed by cyclization of 3 under acidic conditions. The 2-chloropyridine 4 a reacts with nucleophiles under substitution. The treatment of ethyl dichloropropionate 1 b with C - H-acidic compounds provided the cyclopropanes 11 or 12, the configurations of which were determined by C-13-NMR spectroscopy. The results of the X-ray structure analysis of 8 c are discussed.
VIETH, SIEGFRIED;JAHNISCH, KLAUS, J. PRAKT. CHEM., 332,(1990) N, C. 687-692
作者:VIETH, SIEGFRIED、JAHNISCH, KLAUS
DOI:——
日期:——
JAHNISCH, K.;SCHWERTNER, S.;SEEBOTH, H., J. PRAKT. CHEM., 330,(1988) N 3, C. 361-366