Skip to content
2000
Volume 6, Issue 3
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

With DL-valinol, 3-amino-1-propanol and o-aminothiophenol, aroyl(bi/tri)cyclic lactones 1 and 2 were cyclized to isoindole- 4-6, 8, 9, pyrimidinone- 10 or thiazepine- 7 condensed heterocycles. The ketal lactone 3 furnished the benzthiazoloisoindole 9 and mixtures of epimeric hydroxyphthalazinoquinazolinones 11 and 12. The structures were established by means of 1H and 13C NMR spectroscopy and in some cases by X-ray crystallography.

Loading

Article metrics loading...

/content/journals/loc/10.2174/157017809787893136
2009-04-01
2025-09-16
Loading full text...

Full text loading...

/content/journals/loc/10.2174/157017809787893136
Loading

  • Article Type:
    Research Article
Keyword(s): 1,3-oxazines; Cycloalkane lactones; Isoindolones; NMR; Stereostructure; Thiazoles; X-ray
This is a required field
Please enter a valid email address
Approval was a Success
Invalid data
An Error Occurred
Approval was partially successful, following selected items could not be processed due to error
Please enter a valid_number test