N-Propylimidazolidinetrione and N-methyl-N′-phenylethylimidazolidinetrione

Ryouko Yoshihara, Hiroyuki Hosomi, Hiromu Aoyama, Shigeru Ohba

Research output: Contribution to journalArticle

3 Citations (Scopus)

Abstract

In crystals of N-propylimidazolidinetrione, C6H8N2O3, (I), and N-methyl-N′-phenylethylimidazolidinetrione, C12H12N2O3, (II), the N-alkyl side chains have trans conformations. Photoirradiation of (I) gives the N-allyl derivative both in solution and in the solid state. (II) is photoreactive, yielding a tricyclic compound in solution, but not in the solid state. The photostability of (II) in the crystalline state may be due to the reaction cavity which does not allow the N′-phenylethyl moiety to make a large conformational change for cyclization.

Original languageEnglish
Pages (from-to)594-596
Number of pages3
JournalActa Crystallographica Section C: Crystal Structure Communications
Volume55
Issue number4
DOIs
Publication statusPublished - 1999 Apr 15

ASJC Scopus subject areas

  • Biochemistry, Genetics and Molecular Biology(all)

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