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Quoted phrase not found in phrase index: "2-phenyl-1,3-indanedione"
Page 1
Photoinduced alpha-Cleavage of 2-Azido-2-phenyl-1,3-indandione at Cryogenic Temperatures.
Banerjee U, Sarkar SK, Krause JA, Karney WL, Abe M, Gudmundsdottir AD. Banerjee U, et al. Org Lett. 2020 Oct 16;22(20):7885-7890. doi: 10.1021/acs.orglett.0c02794. Epub 2020 Sep 25. Org Lett. 2020. PMID: 32975421
To expand the utility of alpha-cleavage at cryogenic temperatures, we investigated the photoreactivity of 2-azido-2-phenyl-1,3-indandione (1). EPR spectroscopy revealed that irradiating 1 in 2-methyltetrahydrofuran (mTHF) matrices forms alkylnit …
To expand the utility of alpha-cleavage at cryogenic temperatures, we investigated the photoreactivity of 2-azido-2-phenyl- …
[Production of 2-phenyl-1,3-indandione].
DZENITIS IaR, ZILE IN, STRAZDIN'VF, SHTERN SF. DZENITIS IaR, et al. Med Prom SSSR. 1962 Mar;3:26-7. Med Prom SSSR. 1962. PMID: 13888872 Russian. No abstract available.
Pharmacokinetics of 2-phenyl-1,3-indandione in the rat after i.v. and oral administration.
de Vries J, Verboom CN, Groot EJ, Nauta WT, Wattel E. de Vries J, et al. Eur J Drug Metab Pharmacokinet. 1979;4(4):225-9. doi: 10.1007/BF03189431. Eur J Drug Metab Pharmacokinet. 1979. PMID: 535602
The pharmacokinetics of the anticoagulant drug, 2-phenyl-1,3-indandione, after i.v and oral administration in the rat might be best described as a non-linear open two-compartment model with elimination fromthe peripheral compartment. ...
The pharmacokinetics of the anticoagulant drug, 2-phenyl-1,3-indandione, after i.v and oral administratio …
Kinetics and mechanism of ionization of the carbon acids 4'-substituted 2-phenyl-1,3-indandiones.
Stella VJ, Gish R. Stella VJ, et al. J Pharm Sci. 1979 Aug;68(8):1047-9. doi: 10.1002/jps.2600680833. J Pharm Sci. 1979. PMID: 39157
The ionization kinetics of three 4'-substituted 2-phenyl-1,3-indandiones, 4'-chloro-, 4'-methoxy-, and 2-phenyl-1,3-indandione itself, were studied at 25 degrees and ionic strength 0.1 using stopped-flow spectrometry and a pH jump technique. ...
The ionization kinetics of three 4'-substituted 2-phenyl-1,3-indandiones, 4'-chloro-, 4'-methoxy-, and 2-phenyl-1,3
Electrochemical oxidation of 2,3-dimethylhydroquinone in the presence of 1,3-dicarbonyl compounds.
Hosseiny Davarani SS, Nematollahi D, Shamsipur M, Najafi NM, Masoumi L, Ramyar S. Hosseiny Davarani SS, et al. J Org Chem. 2006 Mar 3;71(5):2139-42. doi: 10.1021/jo0523767. J Org Chem. 2006. PMID: 16497004
The electrooxidation of 2,3-dimethylhydroquinone (1) has been studied in the presence of 2-phenyl-1,3-indandione (3a), 3-hydroxy-1H-phenalen-1-one (3b), and 2-chloro-5,5-dimethyl-1,3-cyclohexanedione (3c) as CH acid nucleophiles in water/acetoni …
The electrooxidation of 2,3-dimethylhydroquinone (1) has been studied in the presence of 2-phenyl-1,3-indandi
Behaviour of 2-substituted 1,3-indandiones towards aldimines.
Afsah EM, Hamama WS, Etman HA, Sayed-Ahmed AF. Afsah EM, et al. Boll Chim Farm. 2001 Jan-Feb;140(1):46-52. Boll Chim Farm. 2001. PMID: 11338778
On the other hand, treatment of 2-acetyl-1,3-indandione (9) with aldimines gave compounds (11,12,14). The reaction of 2-phenyl-1,3-indandione (15) with aldimines gave the arylamino and the ethylene diamino derivatives (17, 18). ...
On the other hand, treatment of 2-acetyl-1,3-indandione (9) with aldimines gave compounds (11,12,14). The reaction of 2-phenyl
Ionization kinetics of the carbon acid phenindione.
Stella VJ, Gish R. Stella VJ, et al. J Pharm Sci. 1979 Aug;68(8):1042-7. doi: 10.1002/jps.2600680832. J Pharm Sci. 1979. PMID: 39156
The ionization kinetics of carbon acids are slow relative to those of classical acids and bases. Phenindione (2-phenyl-1,3-indandione) is a 1,3-diketone carbon acid of macroscopic experimental pKa 4.09 at 25 degrees and ionic strength 0.1. ...
The ionization kinetics of carbon acids are slow relative to those of classical acids and bases. Phenindione (2-phenyl-1
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