On hydrogen bonding in the intramolecularly chelated tautomers of enolic malondialdehyde and its mono- and dithio-analogues
Author:
Publisher
Royal Society of Chemistry (RSC)
Link
http://pubs.rsc.org/en/content/articlepdf/1980/P2/P29800001080
Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献
1. Symmetry breaking in the axial symmetrical configurations of enolic propanedial, propanedithial, and propanediselenal: pseudo Jahn–Teller effect versus the resonance-assisted hydrogen bond theory;Canadian Journal of Chemistry;2015-06
2. Ab initio study of intra- and intermolecular H-bond energies in π-conjugated molecular systems;Journal of Molecular Structure: THEOCHEM;2005-08
3. Gas phase ionization of 1,3-propanedial tautomeric forms: A theoretical study;Journal of Structural Chemistry;2005-05
4. Ab initio study of the thioketo-enethiol tautomerism of dithiomalondialdehyde and dithioacetylacetone;Journal of Molecular Structure: THEOCHEM;1992-05
5. Intramolecular hydrogen bonding of malondialdehyde and its monothio and dithio analogues studied by the PM3 method;Journal of Molecular Structure: THEOCHEM;1990-09
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