The use of 4-cyanoaminomethylene-2-phenyl-5(4H)-oxazolone in the synthesis of some heteroarylaminomethylene substituted 5(4H)-oxazolones

Synthetic Communications

Volumn 26, Issue 23, 1996, Pages 4487-4494

  Tehovnik, Mojca Dobnikar ^a   Verček, Bojan ^a  

^a UNIVERSITY OF LJUBLJANA   (Slovenia)

Author keywords

[No Author keywords available]

Indexed keywords

OXAZOLE DERIVATIVE;

ARTICLE; CHIRALITY; DRUG SYNTHESIS; NUCLEAR MAGNETIC RESONANCE; REACTION ANALYSIS; TECHNIQUE;

EID: 0009641238     PISSN: 00397911     EISSN: None     Source Type: Journal    
DOI: 10.1080/00397919608003850     Document Type: Article

References (8)

1. Dobnikar Tehovnik, M.; Petrič, A. and Verček, B. Acta Chimica Slovenica, submitted.
2. Cornforth, J. W. In The Chemistry of Penicillin; Clarke, H. T.; Johnson, J. R.; Robinson, R.; Eds.; Princeton University Press: Princeton, 1949; pp 688-848.
3. Rappoport, Z. In The Chemistry of the Cyano Group; Patai, S., Ed.; Interscience, London, 1970; pp 239-421.
4. Reiter, J. Org. Prep. Proc. Int. 1988, 20, 465.
5. Dobnikar, M.; Kočevar, M.; Polanc, S.; Tišler, M. and Verček, B. Heterocycles 1989, 29, 281.
6. Tikdari, A. M.; Tripathy, P. K. and Mukerjee, A. K. J. Chem. Soc. Perkin Trans. I 1988, 1659.
7. 13C NMR spectra is smaller than 5 Hz for compounds 4, 9, and 11.
8. Boarland, M. P. V. and McOmie, J. F. W. J. Chem. Soc. 1952, 4942.