Advanced Search
Display options
Filter resources
Text Availability
Article type
Publication date
Species
Language
Sex
Age
Showing 1 to 8 of 8 entries
Sorted by: Best Match Show Resources per page
[Pyrazole sulfanilamides. XI. Ethoxy derivatives of phenyl-3-sulfanilamidopyrazole, phenyl-4-sulphanilamidopyrazole, 1-phenyl-5-sulfanilamidopyrazole, 1-phenyl-3-methyl-5-sulfanilamidopyrazole].

Il Farmaco; edizione scientifica

Alberti C, Tironi C.
PMID: 5542665
Farmaco Sci. 1971 Jan;26(1):66-88.

No abstract available.

Cite
Alberti C, Tironi C. Sulfanilammidi pirazoliche. XI. Etossiderivati dell'1-fenil-3-sulfanilammidopirazolo, dell'1-fenil-4-sulfanilammidopirazolo, dell'1-fenil-5-sulfanilammidopirazolo e dell'1-fenyl-3-metil-5-sulfanilammidopirazolo. [Pyrazole sulfanilamides. XI. Ethoxy derivatives of phenyl-3-sulfanilamidopyrazole, phenyl-4-sulphanilamidopyrazole, 1-phenyl-5-sulfanilamidopyrazole, 1-phenyl-3-methyl-5-sulfanilamidopyrazole]. Farmaco Sci. 1971;26(1):66-88
Alberti, C., & Tironi, C. (1971). Sulfanilammidi pirazoliche. XI. Etossiderivati dell'1-fenil-3-sulfanilammidopirazolo, dell'1-fenil-4-sulfanilammidopirazolo, dell'1-fenil-5-sulfanilammidopirazolo e dell'1-fenyl-3-metil-5-sulfanilammidopirazolo. [Pyrazole sulfanilamides. XI. Ethoxy derivatives of phenyl-3-sulfanilamidopyrazole, phenyl-4-sulphanilamidopyrazole, 1-phenyl-5-sulfanilamidopyrazole, 1-phenyl-3-methyl-5-sulfanilamidopyrazole]. Il Farmaco; edizione scientifica, 26(1), 66-88.
Alberti, C, and Tironi, C. "Sulfanilammidi pirazoliche. XI. Etossiderivati dell'1-fenil-3-sulfanilammidopirazolo, dell'1-fenil-4-sulfanilammidopirazolo, dell'1-fenil-5-sulfanilammidopirazolo e dell'1-fenyl-3-metil-5-sulfanilammidopirazolo." [Pyrazole sulfanilamides. XI. Ethoxy derivatives of phenyl-3-sulfanilamidopyrazole, phenyl-4-sulphanilamidopyrazole, 1-phenyl-5-sulfanilamidopyrazole, 1-phenyl-3-methyl-5-sulfanilamidopyrazole]. Il Farmaco; edizione scientifica vol. 26,1 (1971): 66-88.
Alberti C, Tironi C. Sulfanilammidi pirazoliche. XI. Etossiderivati dell'1-fenil-3-sulfanilammidopirazolo, dell'1-fenil-4-sulfanilammidopirazolo, dell'1-fenil-5-sulfanilammidopirazolo e dell'1-fenyl-3-metil-5-sulfanilammidopirazolo. [Pyrazole sulfanilamides. XI. Ethoxy derivatives of phenyl-3-sulfanilamidopyrazole, phenyl-4-sulphanilamidopyrazole, 1-phenyl-5-sulfanilamidopyrazole, 1-phenyl-3-methyl-5-sulfanilamidopyrazole]. Farmaco Sci. 1971 Jan;26(1):66-88. Italian. PMID: 5542665.
Copy Download .nbib Format: NLM
Condensation products of heterocyclically substituted; sulfanilamides with aldehydes.

Helvetica chimica acta

DRUEY J, BECKER A.
PMID: 18100050
Helv Chim Acta. 1948 Dec 01;31(7):2184-92. doi: 10.1002/hlca.19480310740.

No abstract available.

Cite
DRUEY J, BECKER A. Kondensationsprodukte von heterocyclisch substituierten; Sulfanilamiden mit Aldehyden. Condensation products of heterocyclically substituted; sulfanilamides with aldehydes. Helv Chim Acta. 1948;31(7):2184-92doi: 10.1002/hlca.19480310740.
DRUEY, J., & BECKER, A. (1948). Kondensationsprodukte von heterocyclisch substituierten; Sulfanilamiden mit Aldehyden. Condensation products of heterocyclically substituted; sulfanilamides with aldehydes. Helvetica chimica acta, 31(7), 2184-92. https://doi.org/10.1002/hlca.19480310740
DRUEY, J, and BECKER, A. "Kondensationsprodukte von heterocyclisch substituierten; Sulfanilamiden mit Aldehyden." Condensation products of heterocyclically substituted; sulfanilamides with aldehydes. Helvetica chimica acta vol. 31,7 (1948): 2184-92. doi: https://doi.org/10.1002/hlca.19480310740
DRUEY J, BECKER A. Kondensationsprodukte von heterocyclisch substituierten; Sulfanilamiden mit Aldehyden. Condensation products of heterocyclically substituted; sulfanilamides with aldehydes. Helv Chim Acta. 1948 Dec 01;31(7):2184-92. doi: 10.1002/hlca.19480310740. German. PMID: 18100050.
Copy Download .nbib Format: NLM
Hyperbranched Polyglycerol Functionalized Silica Stationary Phase for Hydrophilic Interaction Liquid Chromatography.

Analytical sciences : the international journal of the Japan Society for Analytical Chemistry

Li H, Zhang X, Zhang L, Cang H, Kong F, Fan D, Wang W.
PMID: 29643306
Anal Sci. 2018;34(4):433-438. doi: 10.2116/analsci.17P486.

Surface-initiated anionic-ring-opening multibranching polymerization was employed to prepare a hyperbranched polyglycerol (HPG) functionalized silica stationary phase for hydrophilic interaction liquid chromatography (HILIC). The obtained stationary phase was characterized by Fourier-transform infrared spectrometry (FT-IR) and thermogravimetric analysis (TGA). The chromatographic...

Cite
Li H, Zhang X, Zhang L, et al. Hyperbranched Polyglycerol Functionalized Silica Stationary Phase for Hydrophilic Interaction Liquid Chromatography. Anal Sci. 2018;34(4):433-438doi: 10.2116/analsci.17P486.
Li, H., Zhang, X., Zhang, L., Cang, H., Kong, F., Fan, D., & Wang, W. (2018). Hyperbranched Polyglycerol Functionalized Silica Stationary Phase for Hydrophilic Interaction Liquid Chromatography. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 34(4), 433-438. https://doi.org/10.2116/analsci.17P486
Li, Hengye, et al. "Hyperbranched Polyglycerol Functionalized Silica Stationary Phase for Hydrophilic Interaction Liquid Chromatography." Analytical sciences : the international journal of the Japan Society for Analytical Chemistry vol. 34,4 (2018): 433-438. doi: https://doi.org/10.2116/analsci.17P486
Li H, Zhang X, Zhang L, Cang H, Kong F, Fan D, Wang W. Hyperbranched Polyglycerol Functionalized Silica Stationary Phase for Hydrophilic Interaction Liquid Chromatography. Anal Sci. 2018;34(4):433-438. doi: 10.2116/analsci.17P486. PMID: 29643306.
Copy Download .nbib Format: NLM
[Combination of dispersive liquid-liquid microextraction based on ionic liquid and pre-column fluorescence derivatization-high performance liquid chromatography for determination of eight sulfonamides in water samples].

Se pu = Chinese journal of chromatography

Wu C, Lei J, Li Y, Wang Y, Chen D, Gong J.
PMID: 25902644
Se Pu. 2014 Dec;32(12):1362-7. doi: 10.3724/sp.j.1123.2014.08006.

Dispersive liquid-liquid microextraction based on ionic liquid coupled with high performance liquid chromatography (HPLC) and pre-column fluorescent derivatization method (IL-DLLME-HPLC-FL) was developed for the determination of eight sulfonamides (SAs). The influence of IL-DLLME parameters on extraction efficiency and the...

Cite
Wu C, Lei J, Li Y, et al. [Combination of dispersive liquid-liquid microextraction based on ionic liquid and pre-column fluorescence derivatization-high performance liquid chromatography for determination of eight sulfonamides in water samples]. Se Pu. 2014;32(12):1362-7doi: 10.3724/sp.j.1123.2014.08006.
Wu, C., Lei, J., Li, Y., Wang, Y., Chen, D., & Gong, J. (2014). [Combination of dispersive liquid-liquid microextraction based on ionic liquid and pre-column fluorescence derivatization-high performance liquid chromatography for determination of eight sulfonamides in water samples]. Se pu = Chinese journal of chromatography, 32(12), 1362-7. https://doi.org/10.3724/sp.j.1123.2014.08006
Wu, Cuiqin, et al. "[Combination of dispersive liquid-liquid microextraction based on ionic liquid and pre-column fluorescence derivatization-high performance liquid chromatography for determination of eight sulfonamides in water samples]." Se pu = Chinese journal of chromatography vol. 32,12 (2014): 1362-7. doi: https://doi.org/10.3724/sp.j.1123.2014.08006
Wu C, Lei J, Li Y, Wang Y, Chen D, Gong J. [Combination of dispersive liquid-liquid microextraction based on ionic liquid and pre-column fluorescence derivatization-high performance liquid chromatography for determination of eight sulfonamides in water samples]. Se Pu. 2014 Dec;32(12):1362-7. doi: 10.3724/sp.j.1123.2014.08006. Chinese. PMID: 25902644.
Copy Download .nbib Format: NLM
Preparation, characterization, and application of a new stationary phase containing different kinds of amine groups.

Analytical and bioanalytical chemistry

Xu L, Peng R, Guan X, Tang W, Liu X, Zhang H.
PMID: 23907685
Anal Bioanal Chem. 2013 Oct;405(25):8311-8. doi: 10.1007/s00216-013-7243-0. Epub 2013 Aug 02.

A new stationary phase containing primary amine and tertiary amine groups was synthesized and its structure was confirmed by infrared spectra, elemental analysis, and zeta potential. This new material was packed into a stainless steel column and the effect...

Cite
Xu L, Peng R, Guan X, et al. Preparation, characterization, and application of a new stationary phase containing different kinds of amine groups. Anal Bioanal Chem. 2013;405(25):8311-8doi: 10.1007/s00216-013-7243-0.
Xu, L., Peng, R., Guan, X., Tang, W., Liu, X., & Zhang, H. (2013). Preparation, characterization, and application of a new stationary phase containing different kinds of amine groups. Analytical and bioanalytical chemistry, 405(25), 8311-8. https://doi.org/10.1007/s00216-013-7243-0
Xu, Luan, et al. "Preparation, characterization, and application of a new stationary phase containing different kinds of amine groups." Analytical and bioanalytical chemistry vol. 405,25 (2013): 8311-8. doi: https://doi.org/10.1007/s00216-013-7243-0
Xu L, Peng R, Guan X, Tang W, Liu X, Zhang H. Preparation, characterization, and application of a new stationary phase containing different kinds of amine groups. Anal Bioanal Chem. 2013 Oct;405(25):8311-8. doi: 10.1007/s00216-013-7243-0. Epub 2013 Aug 02. PMID: 23907685.
Copy Download .nbib Format: NLM
Imidazolium ionic liquid-enhanced poly(quinine)-modified silica as a new multi-mode chromatographic stationary phase for separation of achiral and chiral compounds.

Talanta

Zhou H, Chen J, Li H, Quan K, Zhang Y, Qiu H.
PMID: 32070598
Talanta. 2020 May 01;211:120743. doi: 10.1016/j.talanta.2020.120743. Epub 2020 Jan 15.

In this work, a novel imidazolium ionic liquid-functionalized poly(quinine)-modified silica stationary phase (Sil-PQn-MIm) was successfully synthesized via surface radical chain transfer and nucleophilic substitution reaction. The modified silica was confirmed by series of characterizations including Fourier transform infrared spectroscopy...

Cite
Zhou H, Chen J, Li H, et al. Imidazolium ionic liquid-enhanced poly(quinine)-modified silica as a new multi-mode chromatographic stationary phase for separation of achiral and chiral compounds. Talanta. 2020;211:120743doi: 10.1016/j.talanta.2020.120743.
Zhou, H., Chen, J., Li, H., Quan, K., Zhang, Y., & Qiu, H. (2020). Imidazolium ionic liquid-enhanced poly(quinine)-modified silica as a new multi-mode chromatographic stationary phase for separation of achiral and chiral compounds. Talanta, 211120743. https://doi.org/10.1016/j.talanta.2020.120743
Zhou, Hang, et al. "Imidazolium ionic liquid-enhanced poly(quinine)-modified silica as a new multi-mode chromatographic stationary phase for separation of achiral and chiral compounds." Talanta vol. 211 (2020): 120743. doi: https://doi.org/10.1016/j.talanta.2020.120743
Zhou H, Chen J, Li H, Quan K, Zhang Y, Qiu H. Imidazolium ionic liquid-enhanced poly(quinine)-modified silica as a new multi-mode chromatographic stationary phase for separation of achiral and chiral compounds. Talanta. 2020 May 01;211:120743. doi: 10.1016/j.talanta.2020.120743. Epub 2020 Jan 15. PMID: 32070598.
Copy Download .nbib Format: NLM
Synthesis and Characterization of Bioactive Acylpyrazolone Sulfanilamides and Their Transition Metal Complexes: Single Crystal Structure of 4-Benzoyl-3-methyl-1-phenyl-2-pyrazolin-5-one Sulfanilamide.

Bioinorganic chemistry and applications

Idemudia OG, Sadimenko AP, Afolayan AJ, Hosten EC.
PMID: 26106285
Bioinorg Chem Appl. 2015;2015:717089. doi: 10.1155/2015/717089. Epub 2015 May 27.

Two Schiff base ligands Ampp-Sn 1 and Bmpp-Sn 2, afforded by a condensation reaction between sulfanilamide and the respective acylpyrazolone carbonyl precursors, their Mn(II), Co(II), Ni(II), and Cu(II) complexes prepared by the reaction of ligands and corresponding metal salts...

Cite
Idemudia OG, Sadimenko AP, Afolayan AJ, et al. Synthesis and Characterization of Bioactive Acylpyrazolone Sulfanilamides and Their Transition Metal Complexes: Single Crystal Structure of 4-Benzoyl-3-methyl-1-phenyl-2-pyrazolin-5-one Sulfanilamide. Bioinorg Chem Appl. 2015;2015:717089doi: 10.1155/2015/717089.
Idemudia, O. G., Sadimenko, A. P., Afolayan, A. J., & Hosten, E. C. (2015). Synthesis and Characterization of Bioactive Acylpyrazolone Sulfanilamides and Their Transition Metal Complexes: Single Crystal Structure of 4-Benzoyl-3-methyl-1-phenyl-2-pyrazolin-5-one Sulfanilamide. Bioinorganic chemistry and applications, 2015717089. https://doi.org/10.1155/2015/717089
Idemudia, Omoruyi G, et al. "Synthesis and Characterization of Bioactive Acylpyrazolone Sulfanilamides and Their Transition Metal Complexes: Single Crystal Structure of 4-Benzoyl-3-methyl-1-phenyl-2-pyrazolin-5-one Sulfanilamide." Bioinorganic chemistry and applications vol. 2015 (2015): 717089. doi: https://doi.org/10.1155/2015/717089
Idemudia OG, Sadimenko AP, Afolayan AJ, Hosten EC. Synthesis and Characterization of Bioactive Acylpyrazolone Sulfanilamides and Their Transition Metal Complexes: Single Crystal Structure of 4-Benzoyl-3-methyl-1-phenyl-2-pyrazolin-5-one Sulfanilamide. Bioinorg Chem Appl. 2015;2015:717089. doi: 10.1155/2015/717089. Epub 2015 May 27. PMID: 26106285; PMCID: PMC4461752.
Copy Download .nbib Format: NLM
N(4)Methyl and N(4)Dimethyl Substituted Sulfanilamides: Synthesis, and Pharmacological and Therapeutic Properties.

The Yale journal of biology and medicine

Lewis RA, Tager M.
PMID: 21433924
Yale J Biol Med. 1940 Oct;13(1):111-5.

No abstract available.

Cite
Lewis RA, Tager M. N(4)Methyl and N(4)Dimethyl Substituted Sulfanilamides: Synthesis, and Pharmacological and Therapeutic Properties. Yale J Biol Med. 1940;13(1):111-5
Lewis, R. A., & Tager, M. (1940). N(4)Methyl and N(4)Dimethyl Substituted Sulfanilamides: Synthesis, and Pharmacological and Therapeutic Properties. The Yale journal of biology and medicine, 13(1), 111-5.
Lewis, R A, and Tager, M. "N(4)Methyl and N(4)Dimethyl Substituted Sulfanilamides: Synthesis, and Pharmacological and Therapeutic Properties." The Yale journal of biology and medicine vol. 13,1 (1940): 111-5.
Lewis RA, Tager M. N(4)Methyl and N(4)Dimethyl Substituted Sulfanilamides: Synthesis, and Pharmacological and Therapeutic Properties. Yale J Biol Med. 1940 Oct;13(1):111-5. PMID: 21433924; PMCID: PMC2602473.
Copy Download .nbib Format: NLM
Showing 1 to 8 of 8 entries