Regioselective alkylations of cyclic 1,3-diketones via metalated dimethylhydrazones


Demir A. , Enders D.

JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG, vol.339, no.6, pp.553-563, 1997 (Journal Indexed in SCI) identifier identifier

  • Publication Type: Article / Article
  • Volume: 339 Issue: 6
  • Publication Date: 1997
  • Doi Number: 10.1002/prac.19973390199
  • Title of Journal : JOURNAL FUR PRAKTISCHE CHEMIE-CHEMIKER-ZEITUNG
  • Page Numbers: pp.553-563

Abstract

Cyclic 1,3- diketones 1 are transformed into their 2,2-dimethylhydrazones 2, which can be alkylated regioselectively at different positions after mono-, di-, tri-, and tetrametalation. Monometalated C-2 unsubstituted hydrazones afford C-2 and N-alkylation, monometalated C-2 substituted hydrazones afford only C-2 alkylation. The regioselectivity of the alkylation of the polymetalated hydrazones follows Hauser's rule according to the sequence: NH- > C-4 Ha > C-5 > C-4 Hb. Hydrolysis of the product hydrazones 3-5 afforded mono-and polyalkylated 1,3- diketones 7 in good yields.