Cyclocondensation of amidines with dimethyl acetylenedicarboxylate: A convenient entry into tetramic acids

Erden, I; Özer, Galip; Hoarau, C; Cao, WG

doi:10.1002/jhet.5570430220

Makale Tam Makale Uluslararası 2006

Cyclocondensation of amidines with dimethyl acetylenedicarboxylate: A convenient entry into tetramic acids

I Erden, Galip Özer, C Hoarau, WG Cao

Journal of Heterocyclic Chemistry Cilt 43 · Sayı 2 · ss. 395–399 · 01.03.2006

DOI ile aç

Özet

Amidines undergo cyclocondensations with dimethyl acetylenedicarboxyl ate (DMAD) to give highly functionalized 5-dialkylamino-4-pyrrolin-3-ones. The products are crystalline, highly colored compounds that are uniquely functionalized and represent advanced intermediates in the construction of several other heterocyles, in particular the biologically active tetramic acids. The synthetic transformations of these compounds to tetramic acids are also described.

Sürdürülebilir Kalkınma Amaçları

SKA 3: Sağlıklı Bireyler

Atıf için künye

Erden, I., Özer, G., Hoarau, C., & Cao, W. (2006). Cyclocondensation of amidines with dimethyl acetylenedicarboxylate: A convenient entry into tetramic acids. Journal of Heterocyclic Chemistry, 43(2), 395–399. https://doi.org/10.1002/jhet.5570430220

BibTeX

@article{erden2006-334674,
  author = {Erden, I and Özer, Galip and Hoarau, C and Cao, WG},
  title = {Cyclocondensation of amidines with dimethyl acetylenedicarboxylate: A convenient entry into tetramic acids},
  journal = {Journal of Heterocyclic Chemistry},
  year = {2006},
  volume = {43},
  number = {2},
  pages = {395--399},
  issn = {0022-152X},
  doi = {10.1002/jhet.5570430220},
  url = {https://akademik.atauni.edu.tr/yayinlar/334674-cyclocondensation-of-amidines-with-dimethyl-acetylenedicarboxylate-a-convenient}
}