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Page 1
The Reimer-Tiemann reaction of m-iodophenol.
KOBAYASHI S, TAGAWA S, NAKAJIMA S. KOBAYASHI S, et al. Chem Pharm Bull (Tokyo). 1963 Jan;11:123-6. doi: 10.1248/cpb.11.123. Chem Pharm Bull (Tokyo). 1963. PMID: 14033928 Free article. No abstract available.
Halogen bonds in some dihalogenated phenols: applications to crystal engineering.
Mukherjee A, Desiraju GR. Mukherjee A, et al. IUCrJ. 2013 Oct 18;1(Pt 1):49-60. doi: 10.1107/S2052252513025657. eCollection 2014 Jan 1. IUCrJ. 2013. PMID: 25075319 Free PMC article.
Crystal structures of the related compounds 4-chloro-3-iodophenol (4) and 3,5-dibromophenol (5) were also determined. A computational survey of the structural landscape was undertaken for (1), (2) and (3), using a crystal structure prediction protocol in space group …
Crystal structures of the related compounds 4-chloro-3-iodophenol (4) and 3,5-dibromophenol (5) were also determined. A comput …
Synthesis, structure-activity relationship of iodinated-4-aryloxymethyl-coumarins as potential anti-cancer and anti-mycobacterial agents.
Basanagouda M, Jambagi VB, Barigidad NN, Laxmeshwar SS, Devaru V, Narayanachar. Basanagouda M, et al. Eur J Med Chem. 2014 Mar 3;74:225-33. doi: 10.1016/j.ejmech.2013.12.061. Epub 2014 Jan 11. Eur J Med Chem. 2014. PMID: 24463645
A series of new iodinated-4-aryloxymethylcoumarins 6, 8 and 10 have been obtained from the reaction of various 4-bromomethylcoumarins 4 with 2-iodophenol 5, 3-iodophenol 7 and 4-iodophenol 9 respectively. All the title compounds were screened for anticancer activity …
A series of new iodinated-4-aryloxymethylcoumarins 6, 8 and 10 have been obtained from the reaction of various 4-bromomethylcoumarins 4 with …
An investigation on the catalytic mechanism of enhanced chemiluminescence: immunochemical applications of this reaction.
Vlasenko SB, Arefyev AA, Klimov AD, Kim BB, Gorovits EL, Osipov AP, Gavrilova EM, Yegorov AM. Vlasenko SB, et al. J Biolumin Chemilumin. 1989 Jul;4(1):164-76. doi: 10.1002/bio.1170040125. J Biolumin Chemilumin. 1989. PMID: 2678913
The stopped-flow technique was used to measure the rate constants for the reactions between the oxidized forms of peroxidase with luminol and the following substrates: p-iodophenol, p-bromophenol, p-clorophenol, o-iodophenol, m-iodophenol, luciferin, and 2-io …
The stopped-flow technique was used to measure the rate constants for the reactions between the oxidized forms of peroxidase with luminol an …
Desulfoluna spongiiphila sp. nov., a dehalogenating bacterium in the Desulfobacteraceae from the marine sponge Aplysina aerophoba.
Ahn YB, Kerkhof LJ, Häggblom MM. Ahn YB, et al. Int J Syst Evol Microbiol. 2009 Sep;59(Pt 9):2133-9. doi: 10.1099/ijs.0.005884-0. Epub 2009 Jul 15. Int J Syst Evol Microbiol. 2009. PMID: 19605712
Strain AA1T was able to dehalogenate several different bromophenols, and 2- and 3-iodophenol, but not monochlorinated or fluorinated phenols. Lactate, pyruvate, fumarate and malate were not utilized without an electron acceptor. ...
Strain AA1T was able to dehalogenate several different bromophenols, and 2- and 3-iodophenol, but not monochlorinated or fluor …
Inductive and resonance effects of substituents adjust the microalgal biodegradation of toxical phenolic compounds.
Papazi A, Kotzabasis K. Papazi A, et al. J Biotechnol. 2008 Jul 31;135(4):366-73. doi: 10.1016/j.jbiotec.2008.05.009. Epub 2008 May 28. J Biotechnol. 2008. PMID: 18597879
This fact combined with the presence of the hydroxyl group in the phenolic ring gave the observed stabilization in the biodegradation results of mono-iodophenols (2-iodophenol approximately 3-iodophenol approximately 4-iodophenol)....
This fact combined with the presence of the hydroxyl group in the phenolic ring gave the observed stabilization in the biodegradation result …
Genetic polymorphism in the human UGT1A6 (planar phenol) UDP-glucuronosyltransferase: pharmacological implications.
Ciotti M, Marrone A, Potter C, Owens IS. Ciotti M, et al. Pharmacogenetics. 1997 Dec;7(6):485-95. doi: 10.1097/00008571-199712000-00007. Pharmacogenetics. 1997. PMID: 9429234
UGT1A6*2 (181 A+ and 184S+) metabolized 4-nitrophenol, 4-tert-butylphenol, 3-ethylphenol/4-ethylphenol, 4-hydroxycoumarin, butylated hydroxy anisole and butylated hydroxy toluene, with the pH 6.4 preference, at only 27-75% of the rate of the wild-type isozyme whereas 1-naphthol, …
UGT1A6*2 (181 A+ and 184S+) metabolized 4-nitrophenol, 4-tert-butylphenol, 3-ethylphenol/4-ethylphenol, 4-hydroxycoumarin, butylated hydroxy …
Palladium-catalyzed cross-coupling reaction of organoindiums with aryl halides in aqueous media.
Takami K, Yorimitsu H, Shinokubo H, Matsubara S, Oshima K. Takami K, et al. Org Lett. 2001 Jun 28;3(13):1997-9. doi: 10.1021/ol015975i. Org Lett. 2001. PMID: 11418033
[reaction: see text] Diaryl-, divinyl-, and dialkylindium proved to be stable in aqueous media and to undergo a palladium-catalyzed cross-coupling reaction with aryl halides in aqueous THF. Treatment of 3-iodophenol with diphenylindium compound, generated from indiu …
[reaction: see text] Diaryl-, divinyl-, and dialkylindium proved to be stable in aqueous media and to undergo a palladium-catalyzed cross-co …