Energy of Intramolecular Hydrogen Bonding in ortho-Hydroxybenzaldehydes, Phenones and Quinones. Transfer of Aromaticity from ipso-Benzene Ring to the Enol System(s)-Reference-Cited by-同舟云学术

Energy of Intramolecular Hydrogen Bonding in ortho-Hydroxybenzaldehydes, Phenones and Quinones. Transfer of Aromaticity from ipso-Benzene Ring to the Enol System(s)

Published:2017-03-18 Issue:3 Volume:22 Page:481
ISSN:1420-3049
Container-title:Molecules
language:en
Short-container-title:Molecules

Author:

Rusinska-Roszak Danuta

Publisher

MDPI AG

Subject

Chemistry (miscellaneous),Analytical Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Molecular Medicine,Drug Discovery,Pharmaceutical Science

Link

http://www.mdpi.com/1420-3049/22/3/481/pdf

Reference73 articles.

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2. The Weak Hydrogen Bond–In Structural Chemistry and Biology;Desiraju,1999

3. Intramolecular hydrogen bonds: common motifs, probabilities of formation and implications for supramolecular organization

4. Evidence for resonance-assisted hydrogen bonding from crystal-structure correlations on the enol form of the .beta.-diketone fragment

5. Evidence for resonance-assisted hydrogen bonding. 4. Covalent nature of the strong homonuclear hydrogen bond. Study of the O-H--O system by crystal structure correlation methods

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