2-Substituted Hexahydroacylanthranils: Synthesis and Selective Reactions with Amines

G. Göndös, L. Gera, G. Dombi, G. Bernáth

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

In contrast to their aromatic analogues, the corresponding saturated diamides 5-9 are formed exclusively when hexahydro-3,1,4-benzoxazinones (3, 4) are reacted with amines. The cyclodehydration reaction of the diamides 5-9 cannot be carried out at arbitrarily high temperatures.

Original languageEnglish
Pages (from-to)1167-1171
Number of pages5
JournalMonatshefte fur Chemie
Volume127
Issue number11
Publication statusPublished - 1996

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Diamide
Amines
Benzoxazines
Temperature

Keywords

  • Hexahydroacylanthranils
  • Hexahydrobenzoxazinones
  • Ring-opening reaction
  • Stereochemistry

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

2-Substituted Hexahydroacylanthranils : Synthesis and Selective Reactions with Amines. / Göndös, G.; Gera, L.; Dombi, G.; Bernáth, G.

In: Monatshefte fur Chemie, Vol. 127, No. 11, 1996, p. 1167-1171.

Research output: Contribution to journalArticle

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