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Chemistry of Heterocyclic Compounds

, Volume 9, Issue 7, pp 871–872 | Cite as

A new method of synthesizing 1,1,3-triphenyl-1H-isoindole

  • R. A. Shaw
  • E. T. Mukmenev
Article
  • 34 Downloads

Abstract

It has been shown that the reaction of benzophenone with 2,2,4,4,6,6-hexakis-(2,2,2,-trifluoroethoxy)-1, 3,5,2,4,6-triazatriphosphorin gives as the main reaction products 1,1,3-triphenyl-1H-isoindole and di(2,2,2-trifluoroethyl)phosphate.

Keywords

Phosphate Organic Chemistry Benzophenone Main Reaction Main Reaction Product 
These keywords were added by machine and not by the authors. This process is experimental and the keywords may be updated as the learning algorithm improves.

Literature cited

  1. 1.
    W. Theilacker, H. J. Bluhm, W. Heitmann, H. Kalenda, and H. J. Meyer, Ann. Chem., 673. 96 (1964).Google Scholar

Copyright information

© Plenum Publishing Corporation 1975

Authors and Affiliations

  • R. A. Shaw
    • 1
    • 2
  • E. T. Mukmenev
    • 1
    • 2
  1. 1.Department of Chemistry, J. Birkbeck CollegeUniversity of LondonUSSR
  2. 2.A. E. Arbuzov Institute of Organic and Physical ChemistryAcademy of Sciences of the USSRKazan

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