Simple assembly of polysubstituted pyrazoles and isoxazoles via ring closure-ring opening domino reaction of 3-acyl-4,5-dihydrofurans with hydrazines and hydroxylamine

Org Biomol Chem. 2016 Mar 14;14(10):2905-15. doi: 10.1039/c5ob02596f.

Abstract

A convenient general approach to 2-(pyrazol-4-yl)- and 2-(isoxazol-4-yl)ethanols based on the Brønsted acid-initiated reaction of 3-acyl-4,5-dihydrofurans with hydrazines or hydroxylamine was developed. Further transformation of the alcohol moiety in 2-(pyrazolyl)ethanols affording 2-(pyrazolyl)ethylamine as potent bioactive compounds as well as pyrazole-substituted derivatives of antitumor alkaloid crispine A was elaborated.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Cyclization
  • Furans / chemistry*
  • Hydrazines / chemistry*
  • Hydroxylamine / chemistry*
  • Isoxazoles / chemistry*
  • Magnetic Resonance Spectroscopy
  • Pyrazoles / chemistry*
  • Spectrometry, Mass, Electrospray Ionization

Substances

  • Furans
  • Hydrazines
  • Isoxazoles
  • Pyrazoles
  • Hydroxylamine