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Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice.

Iranian journal of reproductive medicine

Mangoli E, Talebi AR, Anvari M, Pourentezari M.
PMID: 24639693
Iran J Reprod Med. 2013 Jan;11(1):53-60.

BACKGROUND: Diabetes mellitus (DM), primary or idiopathic is a chronic disorder of the carbohydrate, lipid and protein metabolism. DM may impact male reproductive function at several levels. It is shown that DM has detrimental effects on sperm parameters in...

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Mangoli E, Talebi AR, Anvari M, et al. Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice. Iran J Reprod Med. 2013;11(1):53-60
Mangoli, E., Talebi, A. R., Anvari, M., & Pourentezari, M. (2013). Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice. Iranian journal of reproductive medicine, 11(1), 53-60.
Mangoli, Esmat, et al. "Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice." Iranian journal of reproductive medicine vol. 11,1 (2013): 53-60.
Mangoli E, Talebi AR, Anvari M, Pourentezari M. Effects of experimentally-induced diabetes on sperm parameters and chromatin quality in mice. Iran J Reprod Med. 2013 Jan;11(1):53-60. PMID: 24639693; PMCID: PMC3941382.
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Microwave assisted N-alkylation of amine functionalized crystal-like mesoporous phenylene-silica.

Dalton transactions (Cambridge, England : 2003)

Lourenço MA, Siegel R, Mafra L, Ferreira P.
PMID: 23508286
Dalton Trans. 2013 Apr 28;42(16):5631-4. doi: 10.1039/c3dt32011a.

N-alkylation reaction of amine functionalized phenylene moieties in crystal-like mesoporous silica is successfully achieved with about 87% of conversion in two reaction cycles. A potassium iodide catalyzed method commonly used for the selective N-monoalkylation of aniline is adapted and...

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Lourenço MA, Siegel R, Mafra L, et al. Microwave assisted N-alkylation of amine functionalized crystal-like mesoporous phenylene-silica. Dalton Trans. 2013;42(16):5631-4doi: 10.1039/c3dt32011a.
Lourenço, M. A., Siegel, R., Mafra, L., & Ferreira, P. (2013). Microwave assisted N-alkylation of amine functionalized crystal-like mesoporous phenylene-silica. Dalton transactions (Cambridge, England : 2003), 42(16), 5631-4. https://doi.org/10.1039/c3dt32011a
Lourenço, Mirtha A O, et al. "Microwave assisted N-alkylation of amine functionalized crystal-like mesoporous phenylene-silica." Dalton transactions (Cambridge, England : 2003) vol. 42,16 (2013): 5631-4. doi: https://doi.org/10.1039/c3dt32011a
Lourenço MA, Siegel R, Mafra L, Ferreira P. Microwave assisted N-alkylation of amine functionalized crystal-like mesoporous phenylene-silica. Dalton Trans. 2013 Apr 28;42(16):5631-4. doi: 10.1039/c3dt32011a. PMID: 23508286.
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Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones.

Organic letters

Wang Q, Huang L, Wu X, Jiang H.
PMID: 24237319
Org Lett. 2013 Dec 06;15(23):5940-3. doi: 10.1021/ol4027683. Epub 2013 Nov 15.

A simple and efficient palladium-catalyzed oxidative coupling between 2-alkynyl anilines and allylic alcohols is described by using cheap and green dioxygen as the oxidant. These cross-couplings have a large functional group tolerance and are of higher reactivity toward electron...

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Wang Q, Huang L, Wu X, et al. Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Org Lett. 2013;15(23):5940-3doi: 10.1021/ol4027683.
Wang, Q., Huang, L., Wu, X., & Jiang, H. (2013). Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Organic letters, 15(23), 5940-3. https://doi.org/10.1021/ol4027683
Wang, Qian, et al. "Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones." Organic letters vol. 15,23 (2013): 5940-3. doi: https://doi.org/10.1021/ol4027683
Wang Q, Huang L, Wu X, Jiang H. Nucleopalladation triggering the oxidative Heck reaction: a general strategy to diverse β-indole ketones. Org Lett. 2013 Dec 06;15(23):5940-3. doi: 10.1021/ol4027683. Epub 2013 Nov 15. PMID: 24237319.
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Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications.

Journal of fluorescence

Saeed A, Shabir G, Batool I.
PMID: 24859631
J Fluoresc. 2014 Jul;24(4):1119-27. doi: 10.1007/s10895-014-1392-1. Epub 2014 May 25.

A series of new high light fastness, hot pressing fastness optical brighteners was efficiently synthesized by a three-step approach involving the successive replacement of the three chloro groups of 2,4,6-trichloro-1,3,5-triazine under different conditions of temperature and pH. Thus, 2,4,6-trichloro-1,3,5-triazine...

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Saeed A, Shabir G, Batool I. Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. J Fluoresc. 2014;24(4):1119-27doi: 10.1007/s10895-014-1392-1.
Saeed, A., Shabir, G., & Batool, I. (2014). Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. Journal of fluorescence, 24(4), 1119-27. https://doi.org/10.1007/s10895-014-1392-1
Saeed, Aamer, et al. "Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications." Journal of fluorescence vol. 24,4 (2014): 1119-27. doi: https://doi.org/10.1007/s10895-014-1392-1
Saeed A, Shabir G, Batool I. Novel stilbene-triazine symmetrical optical brighteners: synthesis and applications. J Fluoresc. 2014 Jul;24(4):1119-27. doi: 10.1007/s10895-014-1392-1. Epub 2014 May 25. PMID: 24859631.
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Reaction from isomeric parent ions in the dissociation of dimethylpyrroles.

Journal of the American Society for Mass Spectrometry

Lin T, Asam MR, Glish GL.
PMID: 24203607
J Am Soc Mass Spectrom. 1996 Sep;7(9):930-7. doi: 10.1016/1044-0305(96)00021-9.

The major dissociation pathways of the [M-H](+) (loss of NH3 or CH4) and the [M+H](+) (loss of NH3 or CH3) ions from dimethylpyrroles have been determined to occur from isomeric parent ions. For the [M-H](+) ion (formed by loss...

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Lin T, Asam MR, Glish GL. Reaction from isomeric parent ions in the dissociation of dimethylpyrroles. J Am Soc Mass Spectrom. 1996;7(9):930-7doi: 10.1016/1044-0305(96)00021-9.
Lin, T., Asam, M. R., & Glish, G. L. (1996). Reaction from isomeric parent ions in the dissociation of dimethylpyrroles. Journal of the American Society for Mass Spectrometry, 7(9), 930-7. https://doi.org/10.1016/1044-0305(96)00021-9
Lin, T, et al. "Reaction from isomeric parent ions in the dissociation of dimethylpyrroles." Journal of the American Society for Mass Spectrometry vol. 7,9 (1996): 930-7. doi: https://doi.org/10.1016/1044-0305(96)00021-9
Lin T, Asam MR, Glish GL. Reaction from isomeric parent ions in the dissociation of dimethylpyrroles. J Am Soc Mass Spectrom. 1996 Sep;7(9):930-7. doi: 10.1016/1044-0305(96)00021-9. PMID: 24203607.
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Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines.

Chemistry, an Asian journal

Ran L, Ren ZH, Wang YY, Guan ZH.
PMID: 25202768
Chem Asian J. 2014 Feb;9(2):577-83. doi: 10.1002/asia.201301245.

A novel and efficient palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines has been developed. The reaction tolerates a wide range of functional groups and is a reliable method for the rapid synthesis of a variety of...

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Ran L, Ren ZH, Wang YY, et al. Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines. Chem Asian J. 2014;9(2):577-83doi: 10.1002/asia.201301245.
Ran, L., Ren, Z. H., Wang, Y. Y., & Guan, Z. H. (2014). Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines. Chemistry, an Asian journal, 9(2), 577-83. https://doi.org/10.1002/asia.201301245
Ran, Longfei, et al. "Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines." Chemistry, an Asian journal vol. 9,2 (2014): 577-83. doi: https://doi.org/10.1002/asia.201301245
Ran L, Ren ZH, Wang YY, Guan ZH. Palladium-catalyzed aminocarbonylation of aryl iodides with amides and N-alkyl anilines. Chem Asian J. 2014 Feb;9(2):577-83. doi: 10.1002/asia.201301245. PMID: 25202768.
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Volume increment effect on the photoisomerization of hemicyanine dyes in oligo(ethylene glycol)s.

The journal of physical chemistry. A

Lee Y, Lee M.
PMID: 24266422
J Phys Chem A. 2013 Dec 05;117(48):12878-83. doi: 10.1021/jp4101043. Epub 2013 Nov 25.

We studied the excited-state dynamics of three hemicyanine dyes that undergo internal twisting from the localized excited state to the twisted intramolecular charge-transfer state. The dyes differ in the length of the alkyl chain in the aniline moiety and,...

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Lee Y, Lee M. Volume increment effect on the photoisomerization of hemicyanine dyes in oligo(ethylene glycol)s. J Phys Chem A. 2013;117(48):12878-83doi: 10.1021/jp4101043.
Lee, Y., & Lee, M. (2013). Volume increment effect on the photoisomerization of hemicyanine dyes in oligo(ethylene glycol)s. The journal of physical chemistry. A, 117(48), 12878-83. https://doi.org/10.1021/jp4101043
Lee, Youmin, and Lee, Minyung. "Volume increment effect on the photoisomerization of hemicyanine dyes in oligo(ethylene glycol)s." The journal of physical chemistry. A vol. 117,48 (2013): 12878-83. doi: https://doi.org/10.1021/jp4101043
Lee Y, Lee M. Volume increment effect on the photoisomerization of hemicyanine dyes in oligo(ethylene glycol)s. J Phys Chem A. 2013 Dec 05;117(48):12878-83. doi: 10.1021/jp4101043. Epub 2013 Nov 25. PMID: 24266422.
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N-Arylazetidines: Preparation through Anionic Ring Closure.

The Journal of organic chemistry

Quinodoz P, Drouillat B, Wright K, Marrot J, Couty F.
PMID: 26932242
J Org Chem. 2016 Apr 01;81(7):2899-910. doi: 10.1021/acs.joc.6b00169. Epub 2016 Mar 10.

We report herein an efficient synthesis of diversely substituted N-aryl-2-cyanoazetidines based on an anionic ring-closure reaction. These compounds can be prepared from β-amino alcohols in enantiomerically pure form through a three-step sequence involving (i) copper-catalyzed N-arylation, (ii) N-cyanomethylation of...

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Quinodoz P, Drouillat B, Wright K, et al. N-Arylazetidines: Preparation through Anionic Ring Closure. J Org Chem. 2016;81(7):2899-910doi: 10.1021/acs.joc.6b00169.
Quinodoz, P., Drouillat, B., Wright, K., Marrot, J., & Couty, F. (2016). N-Arylazetidines: Preparation through Anionic Ring Closure. The Journal of organic chemistry, 81(7), 2899-910. https://doi.org/10.1021/acs.joc.6b00169
Quinodoz, Pierre, et al. "N-Arylazetidines: Preparation through Anionic Ring Closure." The Journal of organic chemistry vol. 81,7 (2016): 2899-910. doi: https://doi.org/10.1021/acs.joc.6b00169
Quinodoz P, Drouillat B, Wright K, Marrot J, Couty F. N-Arylazetidines: Preparation through Anionic Ring Closure. J Org Chem. 2016 Apr 01;81(7):2899-910. doi: 10.1021/acs.joc.6b00169. Epub 2016 Mar 10. PMID: 26932242.
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Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization.

Chemical record (New York, N.Y.)

Chelucci G, Porcheddu A.
PMID: 27524555
Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15.

Efficient ruthenium-, rhodium-, palladium-, copper- and iridium-catalysed methodologies have been recently developed for the synthesis of quinolines by the reaction of 2-aminobenzyl alcohols with carbonyl compounds (aldehydes and ketones) or the related alcohols. The reaction is assumed to proceed...

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Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2016;17(2):200-216doi: 10.1002/tcr.201600083.
Chelucci, G., & Porcheddu, A. (2017). Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chemical record (New York, N.Y.), 17(2), 200-216. https://doi.org/10.1002/tcr.201600083
Chelucci, Giorgio, and Porcheddu, Andrea. "Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization." Chemical record (New York, N.Y.) vol. 17,2 (2017): 200-216. doi: https://doi.org/10.1002/tcr.201600083
Chelucci G, Porcheddu A. Synthesis of Quinolines via a Metal-Catalyzed Dehydrogenative N-Heterocyclization. Chem Rec. 2017 Feb;17(2):200-216. doi: 10.1002/tcr.201600083. Epub 2016 Aug 15. PMID: 27524555.
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Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes.

ACS applied materials & interfaces

Duan W, Ronen A, Walker S, Jassby D.
PMID: 27525344
ACS Appl Mater Interfaces. 2016 Aug 31;8(34):22574-84. doi: 10.1021/acsami.6b07196. Epub 2016 Aug 22.

Electrically conducting membranes (ECMs) have been reported to be efficient in fouling prevention and destruction of aqueous chemical compounds. In the current study, highly conductive and anodically stable composite polyaniline-carbon nanotube (PANI-CNT) ultrafiltration (UF) ECMs were fabricated through a...

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Duan W, Ronen A, Walker S, et al. Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes. ACS Appl Mater Interfaces. 2016;8(34):22574-84doi: 10.1021/acsami.6b07196.
Duan, W., Ronen, A., Walker, S., & Jassby, D. (2016). Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes. ACS applied materials & interfaces, 8(34), 22574-84. https://doi.org/10.1021/acsami.6b07196
Duan, Wenyan, et al. "Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes." ACS applied materials & interfaces vol. 8,34 (2016): 22574-84. doi: https://doi.org/10.1021/acsami.6b07196
Duan W, Ronen A, Walker S, Jassby D. Polyaniline-Coated Carbon Nanotube Ultrafiltration Membranes: Enhanced Anodic Stability for In Situ Cleaning and Electro-Oxidation Processes. ACS Appl Mater Interfaces. 2016 Aug 31;8(34):22574-84. doi: 10.1021/acsami.6b07196. Epub 2016 Aug 22. PMID: 27525344.
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Crystal structure and computational study of 2,4-di-chloro-N-[(E)-(5-nitro-thio-phen-2-yl)methyl-idene]aniline.

Acta crystallographica. Section E, Crystallographic communications

Köysal Y, Bülbül H, Gümüş S, Ağar E, Soylu MS.
PMID: 27536410
Acta Crystallogr E Crystallogr Commun. 2016 Jul 22;72:1187-9. doi: 10.1107/S2056989016011816. eCollection 2016 Aug 01.

The title compound, C11H6Cl2N2O2S, is a Schiff base that incorporates an N-bound 2,4-di-chloro-phenyl and a C-bound 5-nitro-thio-phene ring. The mol-ecule is approximately planar, the maximum deviation from the mean plane being 0.233 (4) Å for the C=N N atom....

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Köysal Y, Bülbül H, Gümüş S, et al. Crystal structure and computational study of 2,4-di-chloro-N-[(E)-(5-nitro-thio-phen-2-yl)methyl-idene]aniline. Acta Crystallogr E Crystallogr Commun. 2016;72:1187-9doi: 10.1107/S2056989016011816.
Köysal, Y., Bülbül, H., Gümüş, S., Ağar, E., & Soylu, M. S. (2016). Crystal structure and computational study of 2,4-di-chloro-N-[(E)-(5-nitro-thio-phen-2-yl)methyl-idene]aniline. Acta crystallographica. Section E, Crystallographic communications, 721187-9. https://doi.org/10.1107/S2056989016011816
Köysal, Yavuz, et al. "Crystal structure and computational study of 2,4-di-chloro-N-[(E)-(5-nitro-thio-phen-2-yl)methyl-idene]aniline." Acta crystallographica. Section E, Crystallographic communications vol. 72 (2016): 1187-9. doi: https://doi.org/10.1107/S2056989016011816
Köysal Y, Bülbül H, Gümüş S, Ağar E, Soylu MS. Crystal structure and computational study of 2,4-di-chloro-N-[(E)-(5-nitro-thio-phen-2-yl)methyl-idene]aniline. Acta Crystallogr E Crystallogr Commun. 2016 Jul 22;72:1187-9. doi: 10.1107/S2056989016011816. eCollection 2016 Aug 01. PMID: 27536410; PMCID: PMC4971869.
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A new class of N-H excited-state intramolecular proton transfer (ESIPT) molecules bearing localized zwitterionic tautomers.

Physical chemistry chemical physics : PCCP

Stasyuk AJ, Chen YT, Chen CL, Wu PJ, Chou PT.
PMID: 27537476
Phys Chem Chem Phys. 2016 Sep 21;18(35):24428-36. doi: 10.1039/c6cp05236c. Epub 2016 Aug 18.

A series of new amino (NH)-type intramolecular hydrogen-bonding (H-bonding) compounds have been strategically designed and synthesized. These molecules comprise a 2-(imidazo[1,2-a]pyridin-2-yl)aniline moiety, in which one of the amino hydrogens was replaced with substituents of different electronic properties. This, together...

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Stasyuk AJ, Chen YT, Chen CL, et al. A new class of N-H excited-state intramolecular proton transfer (ESIPT) molecules bearing localized zwitterionic tautomers. Phys Chem Chem Phys. 2016;18(35):24428-36doi: 10.1039/c6cp05236c.
Stasyuk, A. J., Chen, Y. T., Chen, C. L., Wu, P. J., & Chou, P. T. (2016). A new class of N-H excited-state intramolecular proton transfer (ESIPT) molecules bearing localized zwitterionic tautomers. Physical chemistry chemical physics : PCCP, 18(35), 24428-36. https://doi.org/10.1039/c6cp05236c
Stasyuk, Anton J, et al. "A new class of N-H excited-state intramolecular proton transfer (ESIPT) molecules bearing localized zwitterionic tautomers." Physical chemistry chemical physics : PCCP vol. 18,35 (2016): 24428-36. doi: https://doi.org/10.1039/c6cp05236c
Stasyuk AJ, Chen YT, Chen CL, Wu PJ, Chou PT. A new class of N-H excited-state intramolecular proton transfer (ESIPT) molecules bearing localized zwitterionic tautomers. Phys Chem Chem Phys. 2016 Sep 21;18(35):24428-36. doi: 10.1039/c6cp05236c. Epub 2016 Aug 18. PMID: 27537476.
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Showing 1 to 12 of 4690 entries