Synthesis of a Spiro[tetrahydroquinoline‐[1,3,4]thiadiazole] Derivative

László Somogyi, G. Batta, Adrienne L. Tokés

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

The synthesis of 2‐phenyl‐1,2,3,4‐tetrahydroquinolin‐4‐one thiosemicarbazone (2c) and subsequent cyclization to the title compound (3e, R = H) under acetylating conditions are described Their structure was determined by IR‐, 1H‐ and 13C NMR, as well as mass spectral data.

Original languageEnglish
Pages (from-to)1209-1210
Number of pages2
JournalLiebigs Annalen der Chemie
Volume1992
Issue number11
DOIs
Publication statusPublished - 1992

Fingerprint

Thiosemicarbazones
Cyclization
Nuclear magnetic resonance
Derivatives
nuclear magnetic resonance
synthesis
1,3,4-thiadiazole
1,2,3,4-tetrahydroquinoline
Proton Magnetic Resonance Spectroscopy
Carbon-13 Magnetic Resonance Spectroscopy

Keywords

  • 1,3,4‐Thiadiazoline
  • Azaflavanone
  • Quinolines
  • Thiosemicarbazone, cyclization of

ASJC Scopus subject areas

  • Physical and Theoretical Chemistry
  • Organic Chemistry

Cite this

Synthesis of a Spiro[tetrahydroquinoline‐[1,3,4]thiadiazole] Derivative. / Somogyi, László; Batta, G.; Tokés, Adrienne L.

In: Liebigs Annalen der Chemie, Vol. 1992, No. 11, 1992, p. 1209-1210.

Research output: Contribution to journalArticle

Somogyi, László ; Batta, G. ; Tokés, Adrienne L. / Synthesis of a Spiro[tetrahydroquinoline‐[1,3,4]thiadiazole] Derivative. In: Liebigs Annalen der Chemie. 1992 ; Vol. 1992, No. 11. pp. 1209-1210.
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