The Journal of Organic Chemistry

A convenient synthesis of N-vinylpyridinium perchlorate and a study of N-vinylpyridinium cations as Michael reaction acceptors

AR Katritzky, O Rubio

Index: Katritzky, Alan R.; Rubio, Olga Journal of Organic Chemistry, 1983 , vol. 48, # 22 p. 4017 - 4021

Full Text: HTML

Citation Number: 17

Abstract

Katritzky and Rubio system 1 has been its inaccessibility, preparation necessitating the use of Ag20. By an application of our procedure previously reported for the 2, 4, 6-trisubstituted analogues, we now describe a convenient route to l in good yield together with a study of its chemistry, and in particular, concrete evidence for considerable mutual interaction between the pyridinium ring and the vinyl group in both 1 and the triphenyl analogue 2.

Related Articles:

Supramolecular chemistry: molecular recognition and self-assembly using rigid spacer-chelators bearing cofacial terpyridyl palladium (II) complexes separated by 7 Å

[Katritzky, Alan R.; Thind, Sukhpal S. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 1895 - 1900]

Discovery of low nanomolar and subnanomolar inhibitors of the mycobacterial β-carbonic anhydrases Rv1284 and Rv3273

[Katritzky, Alan R.; Manzo, Ruben H. Journal of the Chemical Society, Perkin Transactions 2: Physical Organic Chemistry (1972-1999), 1981 , p. 571 - 575]

More Articles...