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Conformational studies by dynamic NMR. 74.(1) stereomutations of the conformational enantiomers in peri-substituted 1-acylnaphthalenes.

The Journal of organic chemistry

Lunazzi L, Mazzanti A, Munoz Alvarez A.
PMID: 10814215
J Org Chem. 2000 May 19;65(10):3200-6. doi: 10.1021/jo991853g.

Naphthalenes bearing an acyl and a phenyl group in a peri relationship give rise to a pair of enantiomers in the temperature range where the rotations of the acyl group are slow. Such enantiomers were observed by means of...

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Lunazzi L, Mazzanti A, Munoz Alvarez A. Conformational studies by dynamic NMR. 74.(1) stereomutations of the conformational enantiomers in peri-substituted 1-acylnaphthalenes. J Org Chem. 2000;65(10):3200-6doi: 10.1021/jo991853g.
Lunazzi, L., Mazzanti, A., & Munoz Alvarez A. (2000). Conformational studies by dynamic NMR. 74.(1) stereomutations of the conformational enantiomers in peri-substituted 1-acylnaphthalenes. The Journal of organic chemistry, 65(10), 3200-6. https://doi.org/10.1021/jo991853g
Lunazzi, et al. "Conformational studies by dynamic NMR. 74.(1) stereomutations of the conformational enantiomers in peri-substituted 1-acylnaphthalenes." The Journal of organic chemistry vol. 65,10 (2000): 3200-6. doi: https://doi.org/10.1021/jo991853g
Lunazzi L, Mazzanti A, Munoz Alvarez A. Conformational studies by dynamic NMR. 74.(1) stereomutations of the conformational enantiomers in peri-substituted 1-acylnaphthalenes. J Org Chem. 2000 May 19;65(10):3200-6. doi: 10.1021/jo991853g. PMID: 10814215.
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Development of a multiple-class high-resolution gas chromatographic relative retention time model for halogenated environmental contaminants.

Analytical chemistry

Rayne S, Ikonomou MG.
PMID: 12641222
Anal Chem. 2003 Mar 01;75(5):1049-57. doi: 10.1021/ac020406p.

A predictive model for the relative gas chromatographic retention times (GC-RRTs) of the following nine classes of halogenated environmental contaminants was developed: polybrominated diphenyl ethers (PBDEs); polychlorinated diphenyl ethers (PCDEs); polychlorinated biphenyls (PCBs); polychlorinated naphthalenes (PCNs); polychlorinated dibenzo-p-dioxins (PCDDs);...

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Rayne S, Ikonomou MG. Development of a multiple-class high-resolution gas chromatographic relative retention time model for halogenated environmental contaminants. Anal Chem. 2003;75(5):1049-57doi: 10.1021/ac020406p.
Rayne, S., & Ikonomou, M. G. (2003). Development of a multiple-class high-resolution gas chromatographic relative retention time model for halogenated environmental contaminants. Analytical chemistry, 75(5), 1049-57. https://doi.org/10.1021/ac020406p
Rayne, Sierra, and Ikonomou, Michael G. "Development of a multiple-class high-resolution gas chromatographic relative retention time model for halogenated environmental contaminants." Analytical chemistry vol. 75,5 (2003): 1049-57. doi: https://doi.org/10.1021/ac020406p
Rayne S, Ikonomou MG. Development of a multiple-class high-resolution gas chromatographic relative retention time model for halogenated environmental contaminants. Anal Chem. 2003 Mar 01;75(5):1049-57. doi: 10.1021/ac020406p. PMID: 12641222.
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Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase.

Plant physiology

Snedden WA, Arazi T, Fromm H, Shelp BJ.
PMID: 12228492
Plant Physiol. 1995 Jun;108(2):543-549. doi: 10.1104/pp.108.2.543.

Recently, we provided preliminary evidence for calcium (Ca2+)/calmodulin (CaM) stimulation of plant glutamate decarboxylase (GAD; EC 4.1.1.15). In the present study, a detailed characterization of the phenomenon is described. GAD was partially purified from various soybean (Glycine max L....

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Snedden WA, Arazi T, Fromm H, et al. Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase. Plant Physiol. 1995;108(2):543-549doi: 10.1104/pp.108.2.543.
Snedden, W. A., Arazi, T., Fromm, H., & Shelp, B. J. (1995). Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase. Plant physiology, 108(2), 543-549. https://doi.org/10.1104/pp.108.2.543
Snedden, W. A., et al. "Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase." Plant physiology vol. 108,2 (1995): 543-549. doi: https://doi.org/10.1104/pp.108.2.543
Snedden WA, Arazi T, Fromm H, Shelp BJ. Calcium/Calmodulin Activation of Soybean Glutamate Decarboxylase. Plant Physiol. 1995 Jun;108(2):543-549. doi: 10.1104/pp.108.2.543. PMID: 12228492; PMCID: PMC157373.
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Dissection of the Blue-Light-Dependent Signal-Transduction Pathway Involved in Gametic Differentiation of Chlamydomonas reinhardtii.

Plant physiology

Pan JM, Haring MA, Beck CF.
PMID: 12226393
Plant Physiol. 1996 Sep;112(1):303-309. doi: 10.1104/pp.112.1.303.

Gametogenesis of the green alga Chlamydomonas reinhardtii may be viewed as a two-step process that is controlled by the environmental cues of nitrogen deprivation and blue light. Initiation of gametogenesis is induced by nitrogen deprivation, resulting in mating-incompetent pregametes,...

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Pan JM, Haring MA, Beck CF. Dissection of the Blue-Light-Dependent Signal-Transduction Pathway Involved in Gametic Differentiation of Chlamydomonas reinhardtii. Plant Physiol. 1996;112(1):303-309doi: 10.1104/pp.112.1.303.
Pan, J. M., Haring, M. A., & Beck, C. F. (1996). Dissection of the Blue-Light-Dependent Signal-Transduction Pathway Involved in Gametic Differentiation of Chlamydomonas reinhardtii. Plant physiology, 112(1), 303-309. https://doi.org/10.1104/pp.112.1.303
Pan, J. M., et al. "Dissection of the Blue-Light-Dependent Signal-Transduction Pathway Involved in Gametic Differentiation of Chlamydomonas reinhardtii." Plant physiology vol. 112,1 (1996): 303-309. doi: https://doi.org/10.1104/pp.112.1.303
Pan JM, Haring MA, Beck CF. Dissection of the Blue-Light-Dependent Signal-Transduction Pathway Involved in Gametic Differentiation of Chlamydomonas reinhardtii. Plant Physiol. 1996 Sep;112(1):303-309. doi: 10.1104/pp.112.1.303. PMID: 12226393; PMCID: PMC157950.
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Evidence for Opposing Effects of Calmodulin on Cortical Microtubules.

Plant physiology

Fisher DD, Gilroy S, Cyr RJ.
PMID: 12226434
Plant Physiol. 1996 Nov;112(3):1079-1087. doi: 10.1104/pp.112.3.1079.

Microtubule integrity within the cortical array was visualized in detergent-lysed carrot (Daucus carota L.) protoplasts that were exposed to various exogenous levels of Ca2+ and calmodulin (CaM). CaM appears to help stabilize cortical microtubules against the destabilizing action of...

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Fisher DD, Gilroy S, Cyr RJ. Evidence for Opposing Effects of Calmodulin on Cortical Microtubules. Plant Physiol. 1996;112(3):1079-1087doi: 10.1104/pp.112.3.1079.
Fisher, D. D., Gilroy, S., & Cyr, R. J. (1996). Evidence for Opposing Effects of Calmodulin on Cortical Microtubules. Plant physiology, 112(3), 1079-1087. https://doi.org/10.1104/pp.112.3.1079
Fisher, D. D., et al. "Evidence for Opposing Effects of Calmodulin on Cortical Microtubules." Plant physiology vol. 112,3 (1996): 1079-1087. doi: https://doi.org/10.1104/pp.112.3.1079
Fisher DD, Gilroy S, Cyr RJ. Evidence for Opposing Effects of Calmodulin on Cortical Microtubules. Plant Physiol. 1996 Nov;112(3):1079-1087. doi: 10.1104/pp.112.3.1079. PMID: 12226434; PMCID: PMC158034.
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Electrochemical synthesis of novel polypyrrole microstructures.

Chemical communications (Cambridge, England)

Qu L, Shi G.
PMID: 12585393
Chem Commun (Camb). 2003 Jan 21;(2):206-7. doi: 10.1039/b209245j.

Polypyrrole microstructures with unusual morphologies have been synthesized by direct electrochemical oxidation of pyrrole in beta-naphthalenesulfonic acid aqueous solution.

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Qu L, Shi G. Electrochemical synthesis of novel polypyrrole microstructures. Chem Commun (Camb). 2003;(2):206-7doi: 10.1039/b209245j.
Qu, L., & Shi, G. (2003). Electrochemical synthesis of novel polypyrrole microstructures. Chemical communications (Cambridge, England), (2), 206-7. https://doi.org/10.1039/b209245j
Qu, Liangti, and Shi, Gaoquan. "Electrochemical synthesis of novel polypyrrole microstructures." Chemical communications (Cambridge, England) vol. ,2 (2003): 206-7. doi: https://doi.org/10.1039/b209245j
Qu L, Shi G. Electrochemical synthesis of novel polypyrrole microstructures. Chem Commun (Camb). 2003 Jan 21;(2):206-7. doi: 10.1039/b209245j. PMID: 12585393.
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Degradation of substituted naphthalenesulfonic acids by Sphingomonas xenophaga BN6.

Journal of industrial microbiology & biotechnology

Stolz A.
PMID: 11423960
J Ind Microbiol Biotechnol. 1999 Oct;23(4):391-399. doi: 10.1038/sj.jim.2900725.

Sphingomonas xenophaga BN6 was isolated from the river Elbe as a member of a multispecies bacterial culture which mineralized 6-aminonaphthalene-2-sulfonate. Pure cultures of strain BN6 converted a wide range of amino- and hydroxynaphthalene-2-sulfonates via a catabolic pathway similar to...

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Stolz A. Degradation of substituted naphthalenesulfonic acids by Sphingomonas xenophaga BN6. J Ind Microbiol Biotechnol. 1999;23(4):391-399doi: 10.1038/sj.jim.2900725.
Stolz, A. (1999). Degradation of substituted naphthalenesulfonic acids by Sphingomonas xenophaga BN6. Journal of industrial microbiology & biotechnology, 23(4), 391-399. https://doi.org/10.1038/sj.jim.2900725
Stolz, A. "Degradation of substituted naphthalenesulfonic acids by Sphingomonas xenophaga BN6." Journal of industrial microbiology & biotechnology vol. 23,4 (1999): 391-399. doi: https://doi.org/10.1038/sj.jim.2900725
Stolz A. Degradation of substituted naphthalenesulfonic acids by Sphingomonas xenophaga BN6. J Ind Microbiol Biotechnol. 1999 Oct;23(4):391-399. doi: 10.1038/sj.jim.2900725. PMID: 11423960.
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Polychlorinated naphthalenes: an environmental update.

Environmental pollution (Barking, Essex : 1987)

Falandysz J.
PMID: 15093100
Environ Pollut. 1998;101(1):77-90. doi: 10.1016/s0269-7491(98)00023-2.

Polychlorinated naphthalenes (PCNs; CNs) form a complex mixture of up to 75 congeners containing from one to eight chlorine atoms per naphthalene molecule. Chloronaphthalenes are widespread global environmental pollutants which accumulate in biota. All chloronaphthalenes are planar compounds and...

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Falandysz J. Polychlorinated naphthalenes: an environmental update. Environ Pollut. 1998;101(1):77-90doi: 10.1016/s0269-7491(98)00023-2.
Falandysz, J. (1998). Polychlorinated naphthalenes: an environmental update. Environmental pollution (Barking, Essex : 1987), 101(1), 77-90. https://doi.org/10.1016/s0269-7491(98)00023-2
Falandysz, J. "Polychlorinated naphthalenes: an environmental update." Environmental pollution (Barking, Essex : 1987) vol. 101,1 (1998): 77-90. doi: https://doi.org/10.1016/s0269-7491(98)00023-2
Falandysz J. Polychlorinated naphthalenes: an environmental update. Environ Pollut. 1998;101(1):77-90. doi: 10.1016/s0269-7491(98)00023-2. PMID: 15093100.
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Modified sampling and analysis method for large volatility range airborne polycyclic aromatic hydrocarbons (PAH) using gas chromatography-mass spectrometry.

Analytical and bioanalytical chemistry

Wybraniec S, De Jong AP.
PMID: 15048341
Anal Bioanal Chem. 1996 Oct;356(6):396-402. doi: 10.1007/s0021663560396.

A sampling method has been developed for the measurement for polycyclic aromatic hydrocarbons in ambient air by gas chromatography isotope dilution mass spectrometry. The method has been designed to measure the largest possible volatility range of PAHs including the...

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Wybraniec S, De Jong AP. Modified sampling and analysis method for large volatility range airborne polycyclic aromatic hydrocarbons (PAH) using gas chromatography-mass spectrometry. Anal Bioanal Chem. 1996;356(6):396-402doi: 10.1007/s0021663560396.
Wybraniec, S., & De Jong, A. P. (1996). Modified sampling and analysis method for large volatility range airborne polycyclic aromatic hydrocarbons (PAH) using gas chromatography-mass spectrometry. Analytical and bioanalytical chemistry, 356(6), 396-402. https://doi.org/10.1007/s0021663560396
Wybraniec, S, and De Jong, A P. "Modified sampling and analysis method for large volatility range airborne polycyclic aromatic hydrocarbons (PAH) using gas chromatography-mass spectrometry." Analytical and bioanalytical chemistry vol. 356,6 (1996): 396-402. doi: https://doi.org/10.1007/s0021663560396
Wybraniec S, De Jong AP. Modified sampling and analysis method for large volatility range airborne polycyclic aromatic hydrocarbons (PAH) using gas chromatography-mass spectrometry. Anal Bioanal Chem. 1996 Oct;356(6):396-402. doi: 10.1007/s0021663560396. PMID: 15048341.
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Steady-state fluorescence polarization in planar lipid membranes. Experimental and theoretical analysis of the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-Diphenyl-1,3,5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids.

Biophysical chemistry

Frehland E, Kreikenbohm R, Pohl WG.
PMID: 17000423
Biophys Chem. 1982 Apr;15(1):73-86. doi: 10.1016/0301-4622(82)87018-x.

In continuation of earlier work, the steady-state fluorescence polarization in a globally oriented system of planar lipid membranes was analyzed experimentally and theoretically for the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-diphenyl-1,3, 5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids. The theoretical analyses of experiments...

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Frehland E, Kreikenbohm R, Pohl WG. Steady-state fluorescence polarization in planar lipid membranes. Experimental and theoretical analysis of the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-Diphenyl-1,3,5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids. Biophys Chem. 1982;15(1):73-86doi: 10.1016/0301-4622(82)87018-x.
Frehland, E., Kreikenbohm, R., & Pohl, W. G. (1982). Steady-state fluorescence polarization in planar lipid membranes. Experimental and theoretical analysis of the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-Diphenyl-1,3,5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids. Biophysical chemistry, 15(1), 73-86. https://doi.org/10.1016/0301-4622(82)87018-x
Frehland, E, et al. "Steady-state fluorescence polarization in planar lipid membranes. Experimental and theoretical analysis of the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-Diphenyl-1,3,5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids." Biophysical chemistry vol. 15,1 (1982): 73-86. doi: https://doi.org/10.1016/0301-4622(82)87018-x
Frehland E, Kreikenbohm R, Pohl WG. Steady-state fluorescence polarization in planar lipid membranes. Experimental and theoretical analysis of the fluorophores 8-anilino-1-naphthalenesulfonate, 1,6-Diphenyl-1,3,5-hexatriene, dansyllysine-valinomycin and n-(9-anthroyloxy) fatty acids. Biophys Chem. 1982 Apr;15(1):73-86. doi: 10.1016/0301-4622(82)87018-x. PMID: 17000423.
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Occupational exposure: Organochlorine compounds in blood plasma from potentially exposed workers. PCB, PCN, PCDD/PCDF, HCB and methylsulphonyl metabolites of PCB.

Environmental science and pollution research international

Weistrand C, Norén K, Nilsson A.
PMID: 19002410
Environ Sci Pollut Res Int. 1997;4(1):2-9. doi: 10.1007/BF02986256.

Concentrations of polychlorinated biphenyls (PCB), polychlorinated naphthalenes (PCN), polychlorinated dibenzo-p-dioxins (PCDD), polychlorinated dibenzofurans (PCDF), hexachlorobenzene and methylsulphonyl metabolites of PCB were determined in blood plasma from potentially exposed workers and controls. Three of the potentially exposed subjects had worked...

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Weistrand C, Norén K, Nilsson A. Occupational exposure: Organochlorine compounds in blood plasma from potentially exposed workers. PCB, PCN, PCDD/PCDF, HCB and methylsulphonyl metabolites of PCB. Environ Sci Pollut Res Int. 1997;4(1):2-9doi: 10.1007/BF02986256.
Weistrand, C., Norén, K., & Nilsson, A. (1997). Occupational exposure: Organochlorine compounds in blood plasma from potentially exposed workers. PCB, PCN, PCDD/PCDF, HCB and methylsulphonyl metabolites of PCB. Environmental science and pollution research international, 4(1), 2-9. https://doi.org/10.1007/BF02986256
Weistrand, C, et al. "Occupational exposure: Organochlorine compounds in blood plasma from potentially exposed workers. PCB, PCN, PCDD/PCDF, HCB and methylsulphonyl metabolites of PCB." Environmental science and pollution research international vol. 4,1 (1997): 2-9. doi: https://doi.org/10.1007/BF02986256
Weistrand C, Norén K, Nilsson A. Occupational exposure: Organochlorine compounds in blood plasma from potentially exposed workers. PCB, PCN, PCDD/PCDF, HCB and methylsulphonyl metabolites of PCB. Environ Sci Pollut Res Int. 1997;4(1):2-9. doi: 10.1007/BF02986256. PMID: 19002410.
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A highly selective cascade approach to diverse aromatic ring systems from simple aromatic aldehydes and propiolates.

Organic letters

Wang YG, Cui SL, Lin XF.
PMID: 16524313
Org Lett. 2006 Mar 16;8(6):1241-4. doi: 10.1021/ol060143b.

[reaction: see text] A new triethylamine-catalyzed cascade reaction of aromatic aldehydes with propiolates has been developed. This serial multi-bond-forming process furnishes diverse polycyclic aromatic hydrocarbons, including naphthalenes, phenanthrenes, benzofurans, and 2,3,9,9a-tetrahydronaphtha[2,3-b]furans. The chemical outcome of the process depends on...

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Wang YG, Cui SL, Lin XF. A highly selective cascade approach to diverse aromatic ring systems from simple aromatic aldehydes and propiolates. Org Lett. 2006;8(6):1241-4doi: 10.1021/ol060143b.
Wang, Y. G., Cui, S. L., & Lin, X. F. (2006). A highly selective cascade approach to diverse aromatic ring systems from simple aromatic aldehydes and propiolates. Organic letters, 8(6), 1241-4. https://doi.org/10.1021/ol060143b
Wang, Yan-Guang, et al. "A highly selective cascade approach to diverse aromatic ring systems from simple aromatic aldehydes and propiolates." Organic letters vol. 8,6 (2006): 1241-4. doi: https://doi.org/10.1021/ol060143b
Wang YG, Cui SL, Lin XF. A highly selective cascade approach to diverse aromatic ring systems from simple aromatic aldehydes and propiolates. Org Lett. 2006 Mar 16;8(6):1241-4. doi: 10.1021/ol060143b. PMID: 16524313.
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