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The crystal and molecular structure of an unexpected product from an attempted hantzsch pyridine synthesis. Imine‐enamine tautomerism
Author(s) -
Natale N. R.,
Hope Hakon
Publication year - 1986
Publication title -
journal of heterocyclic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.321
H-Index - 59
eISSN - 1943-5193
pISSN - 0022-152X
DOI - 10.1002/jhet.5570230314
Subject(s) - chemistry , tautomer , enamine , imine , benzylamine , pyridine , stereochemistry , yield (engineering) , organic chemistry , catalysis , materials science , metallurgy
Hantzsch conditions with N ‐benzylamine gave carbocycle 3 rather than a dihydropyridine when isoxazolealdehyde 2 was employed.
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