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Synthesis 2008(10): 1541-1544
DOI: 10.1055/s-2008-1072578
DOI: 10.1055/s-2008-1072578
PAPER
© Georg Thieme Verlag Stuttgart · New York
Stereoselective Synthesis of 2-[1-Methylpyridin-2(1H)-ylidene]malononitrile Derivatives
Further Information
Received
23 January 2008
Publication Date:
07 April 2008 (online)
Publication History
Publication Date:
07 April 2008 (online)

Abstract
An efficient synthesis of 2-[1-methylpyridin-2(1H)-ylidene]malononitrile derivatives have been identified, the reactions have been proved to be stereoselective; the spatial location of substituents has been determined.
Key words
1-alkyl-2-chloropyridinium iodide - CH-acids - nitrile group - hydrogen bond - stereoselectivity
- 1
Tomisawa H.Nakano H.Hongo H. Chem. Pharm. Bull. 1988, 5: 1692 - 2
Khoroshilov GE. Chem. Heterocycl. Compd. (Engl. Transl.) 2001, 9: 1141 - 4
Pauls H.Kröhnke F. Chem. Ber. 1977, 110: 1294 -
5a
Boyd GV.Ezekiel AD.Ellis AW. J. Chem. Soc. C 1967, 1866 -
5b
Zagulyaeva OA.Grigorkina OA.Mamatyuk VI.Mamaev VP. Chem. Heterocycl. Compd. (Engl. Transl.) 1984, 1270 - 6
Günther H. NMR Spectroscopy, An Introduction John Wiley; Chichester: 1980.
References
Khoroshilov, G. E.; Demchak, I. V. Abstract of Papers, International Conference Chemistry of Nitrogen Containing Heterocycles CNCH-2006, Kharkiv, Ukraine, Oct 2-7, 2006; 222; http://cnh2006.iflab.kiev.ua/t/static/Page223.pdf.