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Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some …

evaluation

Sondhi SM, Lozach O.
GSID: TXu01aBjYGoJ
SM Sondhi, N Singh, A Kumar, O Lozach… - Bioorganic & medicinal …, 2006 - Elsevier

A series of N-(acridin-9-yl)-4-(benzo[d]imidazol/oxazol-2-yl) benzamides has been synthesized by the condensation of 9-aminoacridine derivatives with benzimidazole or benzoxazole derivatives. Condensation of 2-hydroxy naphthaldehyde with functionalized diamines leads …

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Sondhi, S. M., Singh, N., Kumar, A., Lozach, O., & Meijer, L. (2006). Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases. Bioorganic & medicinal chemistry, 14(11), 3758-3765.
Sondhi, Sham M., et al. "Synthesis, anti-inflammatory, analgesic and kinase (CDK-1, CDK-5 and GSK-3) inhibition activity evaluation of benzimidazole/benzoxazole derivatives and some Schiff’s bases." Bioorganic & medicinal chemistry 14.11 (2006): 3758-3765.
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Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13C and 15N CPMAS NMR investigations.

Magnetic resonance in chemistry : MRC

Jaźwiński J, Kamieński B, Sadlej A.
PMID: 24123364
Magn Reson Chem. 2013 Dec;51(12):788-94. doi: 10.1002/mrc.4017. Epub 2013 Oct 04.

Complexation properties of dimeric rhodium(II) tetracarboxylates have been utilised in chemistry, spectroscopy and organic synthesis. Particularly, the combination of these rhodium salts with multifunctional ligands results in the formation of coordination polymers, and these are of interest because of...

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Jaźwiński J, Kamieński B, Sadlej A. Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13C and 15N CPMAS NMR investigations. Magn Reson Chem. 2013;51(12):788-94doi: 10.1002/mrc.4017.
Jaźwiński, J., Kamieński, B., & Sadlej, A. (2013). Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13C and 15N CPMAS NMR investigations. Magnetic resonance in chemistry : MRC, 51(12), 788-94. https://doi.org/10.1002/mrc.4017
Jaźwiński, Jarosław, et al. "Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13C and 15N CPMAS NMR investigations." Magnetic resonance in chemistry : MRC vol. 51,12 (2013): 788-94. doi: https://doi.org/10.1002/mrc.4017
Jaźwiński J, Kamieński B, Sadlej A. Polymeric adducts of rhodium(II) tetraacetate with aliphatic diamines: natural abundance 13C and 15N CPMAS NMR investigations. Magn Reson Chem. 2013 Dec;51(12):788-94. doi: 10.1002/mrc.4017. Epub 2013 Oct 04. PMID: 24123364.
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Synthesis and Characterization of Heterobenzenacyclo-octaphanes Derived from Cyclotetrabenzoin.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hahn S, Alrayyani M, Sontheim A, Wang X, Rominger F, Miljanić OŠ, Bunz UHF.
PMID: 28474790
Chemistry. 2017 Aug 04;23(44):10543-10550. doi: 10.1002/chem.201701125. Epub 2017 Jun 14.

We describe the modular synthesis and characterization of several substituted N-hetero benzenacyclooctaphanes (BAOs), a new motif for heteroaromatic conjugated macrocycles. The targets were synthesized via condensation of substituted aromatic ortho-diamines with a cyclic octaketone building block in moderate to...

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Hahn S, Alrayyani M, Sontheim A, et al. Synthesis and Characterization of Heterobenzenacyclo-octaphanes Derived from Cyclotetrabenzoin. Chemistry. 2017;23(44):10543-10550doi: 10.1002/chem.201701125.
Hahn, S., Alrayyani, M., Sontheim, A., Wang, X., Rominger, F., Miljanić, O. �. �., & Bunz, U. H. F. (2017). Synthesis and Characterization of Heterobenzenacyclo-octaphanes Derived from Cyclotetrabenzoin. Chemistry (Weinheim an der Bergstrasse, Germany), 23(44), 10543-10550. https://doi.org/10.1002/chem.201701125
Hahn, Sebastian, et al. "Synthesis and Characterization of Heterobenzenacyclo-octaphanes Derived from Cyclotetrabenzoin." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 23,44 (2017): 10543-10550. doi: https://doi.org/10.1002/chem.201701125
Hahn S, Alrayyani M, Sontheim A, Wang X, Rominger F, Miljanić OŠ, Bunz UHF. Synthesis and Characterization of Heterobenzenacyclo-octaphanes Derived from Cyclotetrabenzoin. Chemistry. 2017 Aug 04;23(44):10543-10550. doi: 10.1002/chem.201701125. Epub 2017 Jun 14. PMID: 28474790.
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Heteroatom-rich porous organic polymers constructed by benzoxazine linkage with high carbon dioxide adsorption affinity.

Journal of colloid and interface science

Xu S, He J, Jin S, Tan B.
PMID: 28923743
J Colloid Interface Sci. 2018 Jan 01;509:457-462. doi: 10.1016/j.jcis.2017.09.009. Epub 2017 Sep 07.

We report the synthesis and characterization of a new type of porous organic polymers linked by benzoxazine. The polymers were readily synthesized by condensation reaction of diamines, triphenol and paraformaldehyde. The formation of the linkage and porous structures were...

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Xu S, He J, Jin S, et al. Heteroatom-rich porous organic polymers constructed by benzoxazine linkage with high carbon dioxide adsorption affinity. J Colloid Interface Sci. 2017;509:457-462doi: 10.1016/j.jcis.2017.09.009.
Xu, S., He, J., Jin, S., & Tan, B. (2018). Heteroatom-rich porous organic polymers constructed by benzoxazine linkage with high carbon dioxide adsorption affinity. Journal of colloid and interface science, 509457-462. https://doi.org/10.1016/j.jcis.2017.09.009
Xu, Shuju, et al. "Heteroatom-rich porous organic polymers constructed by benzoxazine linkage with high carbon dioxide adsorption affinity." Journal of colloid and interface science vol. 509 (2018): 457-462. doi: https://doi.org/10.1016/j.jcis.2017.09.009
Xu S, He J, Jin S, Tan B. Heteroatom-rich porous organic polymers constructed by benzoxazine linkage with high carbon dioxide adsorption affinity. J Colloid Interface Sci. 2018 Jan 01;509:457-462. doi: 10.1016/j.jcis.2017.09.009. Epub 2017 Sep 07. PMID: 28923743.
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Langmuir-Blodgett films of perylene bisimide derivatives and fluorescent recognition of diamines.

Physical chemistry chemical physics : PCCP

Shang C, Wang L, An Y, Chen P, Chang X, Qi Y, Kang R, Fang Y.
PMID: 28856364
Phys Chem Chem Phys. 2017 Sep 13;19(35):23898-23904. doi: 10.1039/c7cp04235c.

Fast, sensitive and selective detection of diamines in the vapor phase is of pivotal importance for air and food quality monitoring. In this work, an electron-poor fluorophore, perylene bisimide (PBI), was modified with hydrophilic residues at its bay positions,...

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Shang C, Wang L, An Y, et al. Langmuir-Blodgett films of perylene bisimide derivatives and fluorescent recognition of diamines. Phys Chem Chem Phys. 2017;19(35):23898-23904doi: 10.1039/c7cp04235c.
Shang, C., Wang, L., An, Y., Chen, P., Chang, X., Qi, Y., Kang, R., & Fang, Y. (2017). Langmuir-Blodgett films of perylene bisimide derivatives and fluorescent recognition of diamines. Physical chemistry chemical physics : PCCP, 19(35), 23898-23904. https://doi.org/10.1039/c7cp04235c
Shang, Congdi, et al. "Langmuir-Blodgett films of perylene bisimide derivatives and fluorescent recognition of diamines." Physical chemistry chemical physics : PCCP vol. 19,35 (2017): 23898-23904. doi: https://doi.org/10.1039/c7cp04235c
Shang C, Wang L, An Y, Chen P, Chang X, Qi Y, Kang R, Fang Y. Langmuir-Blodgett films of perylene bisimide derivatives and fluorescent recognition of diamines. Phys Chem Chem Phys. 2017 Sep 13;19(35):23898-23904. doi: 10.1039/c7cp04235c. PMID: 28856364.
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Steric-Hindrance-Induced Regio- and Chemoselective Oxidation of Aromatic Amines.

The Journal of organic chemistry

Patil VV, Shankarling GS.
PMID: 26212905
J Org Chem. 2015 Aug 21;80(16):7876-83. doi: 10.1021/acs.joc.5b00582. Epub 2015 Aug 03.

Unusual regio- and chemoselective oxidation of aromatic amines hindered with ortho substituents (except -NH2, -NHCH3, and -OH) to the corresponding nitro compounds is described by use of nonanebis(peroxoic acid). The mechanistic investigation for selective oxidation of amines ortho-substituted with...

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Patil VV, Shankarling GS. Steric-Hindrance-Induced Regio- and Chemoselective Oxidation of Aromatic Amines. J Org Chem. 2015;80(16):7876-83doi: 10.1021/acs.joc.5b00582.
Patil, V. V., & Shankarling, G. S. (2015). Steric-Hindrance-Induced Regio- and Chemoselective Oxidation of Aromatic Amines. The Journal of organic chemistry, 80(16), 7876-83. https://doi.org/10.1021/acs.joc.5b00582
Patil, Vilas Venunath, and Shankarling, Ganapati Subray. "Steric-Hindrance-Induced Regio- and Chemoselective Oxidation of Aromatic Amines." The Journal of organic chemistry vol. 80,16 (2015): 7876-83. doi: https://doi.org/10.1021/acs.joc.5b00582
Patil VV, Shankarling GS. Steric-Hindrance-Induced Regio- and Chemoselective Oxidation of Aromatic Amines. J Org Chem. 2015 Aug 21;80(16):7876-83. doi: 10.1021/acs.joc.5b00582. Epub 2015 Aug 03. PMID: 26212905.
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The First Modular Route to Core-Chiral Bispidine Ligands and Their Application in Enantioselective Copper(II)-Catalyzed Henry Reactions.

Chemistry (Weinheim an der Bergstrasse, Germany)

Scharnagel D, Müller A, Prause F, Eck M, Goller J, Milius W, Breuning M.
PMID: 26230668
Chemistry. 2015 Aug 24;21(35):12488-500. doi: 10.1002/chem.201502090. Epub 2015 Jul 31.

The first modular and flexible synthesis of core-chiral bispidines was achieved by using an "inside-out" strategy. The key intermediate, a NBoc-activated bispidine lactam, was constructed in enantiomerically pure form from a chirally modified β-amino acid and 2-(acetoxymethyl)acrylonitrile in just...

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Scharnagel D, Müller A, Prause F, et al. The First Modular Route to Core-Chiral Bispidine Ligands and Their Application in Enantioselective Copper(II)-Catalyzed Henry Reactions. Chemistry. 2015;21(35):12488-500doi: 10.1002/chem.201502090.
Scharnagel, D., Müller, A., Prause, F., Eck, M., Goller, J., Milius, W., & Breuning, M. (2015). The First Modular Route to Core-Chiral Bispidine Ligands and Their Application in Enantioselective Copper(II)-Catalyzed Henry Reactions. Chemistry (Weinheim an der Bergstrasse, Germany), 21(35), 12488-500. https://doi.org/10.1002/chem.201502090
Scharnagel, Dagmar, et al. "The First Modular Route to Core-Chiral Bispidine Ligands and Their Application in Enantioselective Copper(II)-Catalyzed Henry Reactions." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,35 (2015): 12488-500. doi: https://doi.org/10.1002/chem.201502090
Scharnagel D, Müller A, Prause F, Eck M, Goller J, Milius W, Breuning M. The First Modular Route to Core-Chiral Bispidine Ligands and Their Application in Enantioselective Copper(II)-Catalyzed Henry Reactions. Chemistry. 2015 Aug 24;21(35):12488-500. doi: 10.1002/chem.201502090. Epub 2015 Jul 31. PMID: 26230668.
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On-surface synthesis of two-dimensional imine polymers with a tunable band gap: a combined STM, DFT and Monte Carlo investigation.

Nanoscale

Xu L, Yu Y, Lin J, Zhou X, Tian WQ, Nieckarz D, Szabelski P, Lei S.
PMID: 27049517
Nanoscale. 2016 Apr 28;8(16):8568-74. doi: 10.1039/c5nr07663c. Epub 2016 Apr 06.

Two-dimensional polymers are of great interest for many potential applications in nanotechnology. The preparation of crystalline 2D polymers with a tunable band gap is critical for their applications in nano-electronics and optoelectronics. In this work, we try to tune...

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Xu L, Yu Y, Lin J, et al. On-surface synthesis of two-dimensional imine polymers with a tunable band gap: a combined STM, DFT and Monte Carlo investigation. Nanoscale. 2016;8(16):8568-74doi: 10.1039/c5nr07663c.
Xu, L., Yu, Y., Lin, J., Zhou, X., Tian, W. Q., Nieckarz, D., Szabelski, P., & Lei, S. (2016). On-surface synthesis of two-dimensional imine polymers with a tunable band gap: a combined STM, DFT and Monte Carlo investigation. Nanoscale, 8(16), 8568-74. https://doi.org/10.1039/c5nr07663c
Xu, Lirong, et al. "On-surface synthesis of two-dimensional imine polymers with a tunable band gap: a combined STM, DFT and Monte Carlo investigation." Nanoscale vol. 8,16 (2016): 8568-74. doi: https://doi.org/10.1039/c5nr07663c
Xu L, Yu Y, Lin J, Zhou X, Tian WQ, Nieckarz D, Szabelski P, Lei S. On-surface synthesis of two-dimensional imine polymers with a tunable band gap: a combined STM, DFT and Monte Carlo investigation. Nanoscale. 2016 Apr 28;8(16):8568-74. doi: 10.1039/c5nr07663c. Epub 2016 Apr 06. PMID: 27049517.
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Corrigendum to 'Interference of iohexol with radioiodine thyroid uptake in the hyperthyroid cat' [ Journal of Feline Medicine and Surgery 10, 460-465].

Journal of feline medicine and surgery

Peremans K, Vandermeulen E, van Hoek I, Daminet S, Vermeire S, Bacher K.
PMID: 28079447
J Feline Med Surg. 2008 Dec;10(6):608. doi: 10.1016/j.jfms.2008.09.002.

No abstract available.

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Peremans K, Vandermeulen E, van Hoek I, et al. Corrigendum to 'Interference of iohexol with radioiodine thyroid uptake in the hyperthyroid cat' [ Journal of Feline Medicine and Surgery 10, 460-465]. J Feline Med Surg. 2008;10(6):608doi: 10.1016/j.jfms.2008.09.002.
Peremans, K., Vandermeulen, E., van Hoek, I., Daminet, S., Vermeire, S., & Bacher, K. (2008). Corrigendum to 'Interference of iohexol with radioiodine thyroid uptake in the hyperthyroid cat' [ Journal of Feline Medicine and Surgery 10, 460-465]. Journal of feline medicine and surgery, 10(6), 608. https://doi.org/10.1016/j.jfms.2008.09.002
Peremans, Kathelijne, et al. "Corrigendum to 'Interference of iohexol with radioiodine thyroid uptake in the hyperthyroid cat' [ Journal of Feline Medicine and Surgery 10, 460-465]." Journal of feline medicine and surgery vol. 10,6 (2008): 608. doi: https://doi.org/10.1016/j.jfms.2008.09.002
Peremans K, Vandermeulen E, van Hoek I, Daminet S, Vermeire S, Bacher K. Corrigendum to 'Interference of iohexol with radioiodine thyroid uptake in the hyperthyroid cat' [ Journal of Feline Medicine and Surgery 10, 460-465]. J Feline Med Surg. 2008 Dec;10(6):608. doi: 10.1016/j.jfms.2008.09.002. PMID: 28079447.
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Hydrogen atom transfer from 1,n-alkanediamines to the cumyloxyl radical. Modulating C-H deactivation through acid-base interactions and solvent effects.

The Journal of organic chemistry

Milan M, Salamone M, Bietti M.
PMID: 24869917
J Org Chem. 2014 Jun 20;79(12):5710-6. doi: 10.1021/jo5008493. Epub 2014 Jun 04.

A time-resolved kinetic study on the effect of trifluoroacetic acid (TFA) on the hydrogen atom transfer (HAT) reactions from 1,n-alkanediamines (R2N(CH2)nNR2, R = H, CH3; n = 1-4), piperazine, and 1,4-dimethylpiperazine to the cumyloxyl radical (CumO(•)), has been carried...

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Milan M, Salamone M, Bietti M. Hydrogen atom transfer from 1,n-alkanediamines to the cumyloxyl radical. Modulating C-H deactivation through acid-base interactions and solvent effects. J Org Chem. 2014;79(12):5710-6doi: 10.1021/jo5008493.
Milan, M., Salamone, M., & Bietti, M. (2014). Hydrogen atom transfer from 1,n-alkanediamines to the cumyloxyl radical. Modulating C-H deactivation through acid-base interactions and solvent effects. The Journal of organic chemistry, 79(12), 5710-6. https://doi.org/10.1021/jo5008493
Milan, Michela, et al. "Hydrogen atom transfer from 1,n-alkanediamines to the cumyloxyl radical. Modulating C-H deactivation through acid-base interactions and solvent effects." The Journal of organic chemistry vol. 79,12 (2014): 5710-6. doi: https://doi.org/10.1021/jo5008493
Milan M, Salamone M, Bietti M. Hydrogen atom transfer from 1,n-alkanediamines to the cumyloxyl radical. Modulating C-H deactivation through acid-base interactions and solvent effects. J Org Chem. 2014 Jun 20;79(12):5710-6. doi: 10.1021/jo5008493. Epub 2014 Jun 04. PMID: 24869917.
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Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines.

Chemistry (Weinheim an der Bergstrasse, Germany)

Kumar R, Arigela RK, Samala S, Kundu B.
PMID: 26525303
Chemistry. 2015 Dec 14;21(51):18828-33. doi: 10.1002/chem.201502956. Epub 2015 Nov 03.

A one-pot protocol for the diversity oriented synthesis of two N-polyheterocycles indoloazepinobenzimidazole and benzimidazotriazolobenzodiazepine from a common N(1)-alkyne-1,2-diamine building block is described. The approach involves sequential formation of benzimidazole through cyclocondensation and oxidation, which is followed by the formation...

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Kumar R, Arigela RK, Samala S, et al. Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines. Chemistry. 2015;21(51):18828-33doi: 10.1002/chem.201502956.
Kumar, R., Arigela, R. K., Samala, S., & Kundu, B. (2015). Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines. Chemistry (Weinheim an der Bergstrasse, Germany), 21(51), 18828-33. https://doi.org/10.1002/chem.201502956
Kumar, Ravi, et al. "Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,51 (2015): 18828-33. doi: https://doi.org/10.1002/chem.201502956
Kumar R, Arigela RK, Samala S, Kundu B. Diversity Oriented Synthesis of Indoloazepinobenzimidazole and Benzimidazotriazolobenzodiazepine from N(1)-Alkyne-1,2-diamines. Chemistry. 2015 Dec 14;21(51):18828-33. doi: 10.1002/chem.201502956. Epub 2015 Nov 03. PMID: 26525303.
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Molecular recognition of aliphatic diamines by 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol.

The Journal of organic chemistry

Yu S, Plunkett W, Kim M, Wu E, Sabat M, Pu L.
PMID: 24283254
J Org Chem. 2013 Dec 20;78(24):12671-80. doi: 10.1021/jo402277p. Epub 2013 Dec 06.

The fluorescent responses of 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol toward a variety of amines have been studied. It was found that the aliphatic primary 1,2- and 1,5-diamines can greatly enhance the fluorescence of this compound, but under the same conditions, primary, secondary, and...

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Yu S, Plunkett W, Kim M, et al. Molecular recognition of aliphatic diamines by 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol. J Org Chem. 2013;78(24):12671-80doi: 10.1021/jo402277p.
Yu, S., Plunkett, W., Kim, M., Wu, E., Sabat, M., & Pu, L. (2013). Molecular recognition of aliphatic diamines by 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol. The Journal of organic chemistry, 78(24), 12671-80. https://doi.org/10.1021/jo402277p
Yu, Shanshan, et al. "Molecular recognition of aliphatic diamines by 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol." The Journal of organic chemistry vol. 78,24 (2013): 12671-80. doi: https://doi.org/10.1021/jo402277p
Yu S, Plunkett W, Kim M, Wu E, Sabat M, Pu L. Molecular recognition of aliphatic diamines by 3,3'-di(trifluoroacetyl)-1,1'-bi-2-naphthol. J Org Chem. 2013 Dec 20;78(24):12671-80. doi: 10.1021/jo402277p. Epub 2013 Dec 06. PMID: 24283254.
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Showing 1 to 12 of 915 entries