Jump to main content
Jump to site search
PLANNED MAINTENANCE Close the message box

Scheduled maintenance work on Wednesday 22nd May 2019 from 11:00 AM to 1:00 PM (GMT).

During this time our website performance may be temporarily affected. We apologise for any inconvenience this might cause and thank you for your patience.


Issue 16, 1997
Previous Article Next Article

Novel synthesis of substituted4′-hydroxy-2,2′:6′,2″-terpyridines

Abstract

4-Substituted-2,6-diacetylpyridines 2–4 have been synthesised; by using the Kröhnke-methodology, chalcone and methylacylpyridinium salts have been reacted to yield 4′-ethoxy-2,2′:6′,2″-terpyridines 5–7. These novel 2,2′:6′,2″-terpyridines are functionalised at C(4′) and possess substituents at C(4), C(5) and C(6) of both terminal pyridines, respectively. The ethyl ether protecting group has been cleaved to obtain 4′-hydroxy-2,2′:6′,2″-terpyridine 8.

Back to tab navigation

Article type: Paper
DOI: 10.1039/A704295G
J. Chem. Soc., Perkin Trans. 1, 1997, 2263-2264

  •   Request permissions

    Novel synthesis of substituted 4′-hydroxy-2,2′:6′,2″-terpyridines

    R. Fallahpour and E. C. Constable, J. Chem. Soc., Perkin Trans. 1, 1997, 2263
    DOI: 10.1039/A704295G

Search articles by author

Spotlight

Advertisements