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297 results

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Page 1
RIFM fragrance ingredient safety assessment, 2-cyclohexen-1-one, 2-methyl-5-propyl-, CAS Registry Number 1447712-18-6.
Api AM, Belsito D, Botelho D, Bruze M, Burton GA Jr, Buschmann J, Cancellieri MA, Dagli ML, Date M, Dekant W, Deodhar C, Fryer AD, Jones L, Joshi K, Kumar M, Lapczynski A, Lavelle M, Lee I, Liebler DC, Moustakas H, Na M, Penning TM, Ritacco G, Romine J, Sadekar N, Schultz TW, Selechnik D, Siddiqi F, Sipes IG, Sullivan G, Thakkar Y, Tokura Y. Api AM, et al. Food Chem Toxicol. 2022 May;163 Suppl 1:113042. doi: 10.1016/j.fct.2022.113042. Epub 2022 Apr 19. Food Chem Toxicol. 2022. PMID: 35452767 No abstract available.
An exceptionally rapid and selective hydrogenation of 2-cyclohexen-1-one in supercritical carbon dioxide.
Chatterjee M, Yokoyama T, Kawanami H, Sato M, Suzuki T. Chatterjee M, et al. Chem Commun (Camb). 2009 Feb 14;(6):701-3. doi: 10.1039/b817295a. Epub 2008 Dec 17. Chem Commun (Camb). 2009. PMID: 19322427
Selective hydrogenation of 2-cyclohexen-1-one over Pt-MCM-41 proceeds at a very high rate and produces cyclohexanone with selectivity of 100% in a batch reactor; a marked increase in the reaction rate (TOF) from 2283 min(-1) to 5051 min(-1) is observed …
Selective hydrogenation of 2-cyclohexen-1-one over Pt-MCM-41 proceeds at a very high rate and produces cyclohexa …
Asymmetric Morita-Baylis-Hillman reaction of arylaldehydes with 2-cyclohexen-1-one catalyzed by chiral bis(thio)urea and DABCO.
Shi M, Liu XG. Shi M, et al. Org Lett. 2008 Mar 20;10(6):1043-6. doi: 10.1021/ol7028806. Epub 2008 Feb 20. Org Lett. 2008. PMID: 18284244
Novel bis(thio)urea organocatalysts were synthesized from axially chiral (R)-(-)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl-2,2'-diamine (H8-BINAM), and their catalytic abilities have been examined in the Morita-Baylis-Hillman reaction of 2-cyclohexen-1- …
Novel bis(thio)urea organocatalysts were synthesized from axially chiral (R)-(-)-5,5',6,6',7,7',8,8'-octahydro-1,1'-binaphthyl-2,2'-diamine …
Selective oxidation of cyclohexanol and 2-cyclohexen-1-ol on O/Au(111): the effect of molecular structure.
Liu X, Friend CM. Liu X, et al. Langmuir. 2010 Nov 2;26(21):16552-7. doi: 10.1021/la1015302. Langmuir. 2010. PMID: 20973586
The two alcohols share common features in their reaction pathways: they are both activated by Bronsted acid-base reactions with adsorbed oxygen. Cyclic ketones, cyclohexanone and 2-cyclohexen-1-one, are the major products, formed from cyclohexanol and …
The two alcohols share common features in their reaction pathways: they are both activated by Bronsted acid-base reactions with adsorbed oxy …
SAR studies of 3-cyclopropanecarbonyloxy-2-cyclohexen-1-one as inhibitors of 4-hydroxyphenylpyruvate dioxygenase.
Lin YL, Wu CS, Lin SW, Huang JL, Sun YS, Yang DY. Lin YL, et al. Bioorg Med Chem. 2002 Mar;10(3):685-90. doi: 10.1016/s0968-0896(01)00322-4. Bioorg Med Chem. 2002. PMID: 11814856
Various 3-cyclopropanecarbonyloxy-2-cyclohexen-1-one 1 derivatives have been synthesized and tested as inhibitors of 4-hydroxyphenylpyruvate dioxygenase (4-HPPD) from pig liver. ...
Various 3-cyclopropanecarbonyloxy-2-cyclohexen-1-one 1 derivatives have been synthesized and tested as inhibitor …
A combined experimental and density functional theory investigation of the hydrogen bonding of 2-cyclohexen-1-one and 3-methyl- 2-cyclohexen-1-one in solvents.
Zhou HQ, Li L, Zhao Y, Wang HG, Zheng X. Zhou HQ, et al. Spectrochim Acta A Mol Biomol Spectrosc. 2019 Feb 5;208:32-39. doi: 10.1016/j.saa.2018.09.045. Epub 2018 Sep 24. Spectrochim Acta A Mol Biomol Spectrosc. 2019. PMID: 30290292
As an important structural motif of pyrimidine bases, the solvent effect of the hydrogen bonding of 2-cyclohexen-1-one (CHO) and 3-methyl- 2-cyclohexen-1-one (3MCHO) and its effect on the frequency shift of the CO stretching …
As an important structural motif of pyrimidine bases, the solvent effect of the hydrogen bonding of 2-cyclohexen-1-o
Cavity Ringdown Spectrum of 2-Cyclohexen-1-one in the CO/Alkenyl CC Stretch Region of the S(1)(n, pi*)-S(0) Vibronic Band System.
Mooneyham AE, McDonnell MP, Drucker S. Mooneyham AE, et al. J Phys Chem A. 2017 Mar 30;121(12):2343-2352. doi: 10.1021/acs.jpca.7b00826. Epub 2017 Mar 20. J Phys Chem A. 2017. PMID: 28260378
The 2-cyclohexen-1-one (2CHO) molecule serves as a prototype for understanding the photochemical properties of conjugated enones. ...
The 2-cyclohexen-1-one (2CHO) molecule serves as a prototype for understanding the photochemical properties of c …
Reaction of morphinone reductase with 2-cyclohexen-1-one and 1-nitrocyclohexene: proton donation, ligand binding, and the role of residues Histidine 186 and Asparagine 189.
Messiha HL, Munro AW, Bruce NC, Barsukov I, Scrutton NS. Messiha HL, et al. J Biol Chem. 2005 Mar 18;280(11):10695-709. doi: 10.1074/jbc.M410595200. Epub 2005 Jan 4. J Biol Chem. 2005. PMID: 15632179 Free article.
We show that both residues are involved in the binding of the reducing nicotinamide coenzyme NADH and also the binding of the oxidizing substrates 2-cyclohexen-1-one and 1-nitrocyclohexene. Reduction of 2-cyclohexen-1-one by …
We show that both residues are involved in the binding of the reducing nicotinamide coenzyme NADH and also the binding of the oxidizing subs …
Immobilization of Ene Reductase in Polyvinyl Alcohol Hydrogel.
Alagöz D, Varan NE, Toprak A, Tükel SS, Yildirim D. Alagöz D, et al. Protein J. 2022 Jun;41(3):394-402. doi: 10.1007/s10930-022-10059-4. Epub 2022 Jun 17. Protein J. 2022. PMID: 35715719
Michaelis-Menten constant and maximum velocity values were 0.25 mM and 1.2 U/mg protein, respectively for the free ER towards 2-cyclohexen-1-one. The corresponding values were 1.5 mM and 0.9 U/mg protein for the entrapped ER. The results of time-course …
Michaelis-Menten constant and maximum velocity values were 0.25 mM and 1.2 U/mg protein, respectively for the free ER towards 2-cy
297 results