Abstract
Amidic hydroxamic acid and
dihydroxamic acid derivatives of maleic, phthalic, fumaric and succinic acids have been prepared and their properties and
reactions studied. In particular suitably oriented derivatives of these systems
have been investigated to ascertain whether they are capable of existing in, or
reacting through, various cyclol tautomers. Attempts to trap the cyclol
tautomers are described and these results, together with other indirect
chemical evidence as well as the spectral data, suggest that the cyclol
tautomer may be present in some cases, in contrast to the corresponding
diamides which do not show similar behaviour.
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14 articles.
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