Image from Google Jackets

A Rapid and Convenient Technique for converting Ketones into their Ethylenedioxy- or Trimethylenedioxy-derivatives, and for making Acetonides

Tipo de material: TextoTextoSeries ; Journal of Chemical Society Perkin Transation 1, p.158-160, 1979Trabajos contenidos:
  • Dann. A.E
  • Davis. J.B
  • Nagler, M.J
Recursos en línea: Resumen: The ethylenedioxy-derivatives (ethylene acetals)of unhindered steroid. triterpene. and other ketones can be prepared by running a mixture of the ketone and ethylene glycol in tetrahydrofuran through an acid ion-exchange column and isolating the derivative from the eluate. This technique is particularly appropriate where such compounds are to be subjected to mass spectrometry but can also be used on a larger scale in synthetic sequences where protection of the carbonyl group is desired. The homologous (cyc!ic trimethylenedioxy-)derivatives. better for the latter purpose in certain cases. can be prepared in the same way. as can the acetonides of 1.3-dihydroxycompounds.
Tags from this library: No tags from this library for this title. Log in to add tags.
Star ratings
    Average rating: 0.0 (0 votes)

The ethylenedioxy-derivatives (ethylene acetals)of unhindered steroid. triterpene. and other ketones can be prepared by running a mixture of the ketone and ethylene glycol in tetrahydrofuran through an acid ion-exchange column and isolating the derivative from the eluate. This technique is particularly appropriate where such compounds are to be subjected to mass spectrometry but can also be used on a larger scale in synthetic sequences where protection of the carbonyl group is desired. The homologous (cyc!ic trimethylenedioxy-)derivatives. better for the latter purpose in certain cases. can be prepared in the same way. as can the acetonides of 1.3-dihydroxycompounds.

There are no comments on this title.

to post a comment.