Issue 11, 1986

7-Phosphanorbornene derivatives as precursors of esters and amides of two-co-ordinate thiophosphenous O-acid

Abstract

Heating thiophosphinate O-esters and thiophosphinamides having the 7-phosphanorbornene framework results in elimination of fragments that are derivatives of thiophosphenous O-acid; they are trapped by cycloaddition with 2,3-dimethylbutadiene to form 2,5-dihydrophospholes.

Article information

Article type
Paper

J. Chem. Soc., Chem. Commun., 1986, 844-846

7-Phosphanorbornene derivatives as precursors of esters and amides of two-co-ordinate thiophosphenous O-acid

L. D. Quin and J. Szewczyk, J. Chem. Soc., Chem. Commun., 1986, 844 DOI: 10.1039/C39860000844

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements