+++ статьи ScDir

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1

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http://dx.doi.org/10.1016/S0165-3253(96)80037-X

Chapter 10 Polyhydric phenols
Studies in Organic Chemistry
Volume 52, 1996, Pages 338-357
Synthetic and Natural Phenols

2

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http://dx.doi.org/10.1016/j.pnmrs.2006.07.001

The use of NMR spectroscopy to study tautomerism
R.M. Claramunt, C. Lópeza, M.D. Santa María, D. Sanz and J. Elguero
Progress in Nuclear Magnetic Resonance Spectroscopy Volume 49, Issues 3-4, 30 November 2006, Pages 169-206

3

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http://dx.doi.org/10.1016/S1010-6030(98)00354-2

Tautomerism of flavonol glucosides: relevance to plant UV protection and flower colour
Gerald J. Smith* and Kenneth R. Markham
Journal of Photochemistry and Photobiology A: Chemistry Volume 118, Issue 2, 30 October 1998, Pages 99-105

4

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http://dx.doi.org/10.1016/S1387-3806(99)00198-0

Two different pathways for unimolecular and for catalyzed keto-enol isomerization of ionized acetophenone1
J Chamot-Rookea, G van der Resta, P Mourguesa and H.E Audier
International Journal of Mass Spectrometry Volumes 195-196, 21 January 2000, Pages 385-392

5

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http://dx.doi.org/10.1016/j.comptc.2010.10.022

Tautomeric preferences and π-electron delocalization for redox forms of phenol
E.D. Raczyńskaa, K. Kolczyńskab and T.M. Stępniewski
Computational and Theoretical Chemistry Volume 963, Issue 1, January 2011, Pages 176-184

6

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http://dx.doi.org/10.1016/j.molstruc.2004.01.033

The intramolecular hydrogen bond in ortho-hydroxy acetophenones
A. Filarowski, A. Kolla, A. Kochela, J. Kalenika and P. E. Hansen
Journal of Molecular Structure Volume 700, Issues 1-3, 20 August 2004, Pages 67-72

7

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http://dx.doi.org/10.1016/0022-2860(90)80394-Y

The influence of steric effects of proton-transfer equilibrium in intramolecular hydrogen bonds
Maria Rospenk
Journal of Molecular Structure Volume 221, 30 April 1990, Pages 109-114

8

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http://dx.doi.org/10.1016/0378-4487(78)80035-1

Theoretical study of the intramolecular hydrogen bonding in benzene derivatives
Enric Canadell, Javier Catalan and Jose I. Fernandez-Alonso
Advances in Molecular Relaxation and Interaction Processes Volume 12, Issue 4, April 1978, Pages 265-287

9

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http://dx.doi.org/10.1016/j.chroma.2006.07.057

Further consideration of the gas–liquid chromatographic method for determining the intramolecular hydrogen bond energies with the example of 2-substituted phenols
Igor M. Skvortsov, Oleg E. Makarov and Evgenii E. Fedorov
Journal of Chromatography A Volume 1132, Issues 1-2, 3 November 2006, Pages 248-255

10

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http://dx.doi.org/10.1016/B978-044453347-0.50094-X

Chapter 4 - Hydroxy aromatics
J.H.P. Tyman
Second Supplements to the 2nd Edition of Rodd's Chemistry of Carbon Compounds
A Modern Comprehensive Treatise 1991, Pages 225-376

11

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http://dx.doi.org/10.1055/s-2007-983880

Highly Efficient and Clean Method for Direct α-Iodination of Aromatic Ketones
Guodong Yina, Meng Gaoa, Nengfang Shea, Shengli Hua, Anxin Wu*a, Yuanjiang Pan
Synthesis 2007(20): 3113-3116

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