Theoretical study of hydroxamic acids

dc.contributor.author	Fitzpatrick, N.J
dc.contributor.author	Mageswaran, R
dc.date.accessioned	2014-01-31T04:54:56Z
dc.date.accessioned	2022-07-11T08:25:13Z
dc.date.available	2014-01-31T04:54:56Z
dc.date.available	2022-07-11T08:25:13Z
dc.date.issued	1989
dc.identifier.issn	02775387
dc.identifier.uri	http://repo.lib.jfn.ac.lk/ujrr/handle/123456789/164
dc.description.abstract	Ab initio molecular orbital calculations on formohydroxamic and acetohydroxamic acids give stabilities in the order: E-keto ≫ Z-keto ≫ Z-enol ≫ E-enol. However, on hydration the E-keto and Z-keto order is reversed, in agreement with NMR results. Methyl substituted forms are also considered, and the importance of hydrogen bonding is noted.	en_US
dc.language.iso	en	en_US
dc.title	Theoretical study of hydroxamic acids	en_US
dc.type	Article	en_US