| Autor: |
Andriyankov, M., Nikitin, M., Afonin, A. |
| Zdroj: |
Bulletin of the Academy of Sciences of The USSR, Division of Chemical Science; 1989, Vol. 38 Issue 9, p1932-1936, 5p |
| Abstrakt: |
The 2-hydroxy-, amino-, and mercaptopyridines and quinolines react with phenyl-acetylene under different catalytic conditions with the formation of the corres-ponding O-, N-, and S-styryl derivatives. In the case of the trans isomer of 1-styryl-2-pyridone, the flat disposition of the olefin fragment and the hetero-cycle with the S-trans conformation of the sytryl group is proposed. All the cis isomers of the 1-styrylpyridones are noncoplanar. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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