Jump to main content
Jump to site search

Issue 14, 1994
Previous Article Next Article

Design and synthesis of transition-state analogues for a cationic cyclisation

Abstract

Transition-state analogues based upon the 6-(hydroxymethyl)-13-azagona-1,3,5(10),8-tetraene structure (e.g., 40) have been designed and synthesized as part of a programme to elicit antibodies capable of catalysing cationic cyclisations. Methodology for conjugating such analogues to proteins has also been developed.

Back to tab navigation

Article type: Paper
DOI: 10.1039/P19940001997
Citation: J. Chem. Soc., Perkin Trans. 1, 1994,0, 1997-2006
  •   Request permissions

    Design and synthesis of transition-state analogues for a cationic cyclisation

    I. M. Bell, C. Abell and F. J. Leeper, J. Chem. Soc., Perkin Trans. 1, 1994, 0, 1997
    DOI: 10.1039/P19940001997

Search articles by author

Spotlight

Advertisements