Skip to content
2000
Volume 3, Issue 2
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

3,5-Diarylisoxazoles and 1,3,5-triarylpyrazolines are synthesized via Michael addition of "hydroxylamine hydrochloride, phenylhydrazine" respectively over chalcones followed by cyclization using K2CO3 as solid support. Reactions are shown to be highly regioselective regardless of the nature of the substituent in the substrates and afforded single isoxazole and pyrazoline isomer in excellent yields.

Loading

Article metrics loading...

/content/journals/loc/10.2174/157017806775224170
2006-02-01
2025-09-10
Loading full text...

Full text loading...

/content/journals/loc/10.2174/157017806775224170
Loading

  • Article Type:
    Research Article
Keyword(s): chalcones; Michael addition; regioselectivity; solid support
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