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Reaction of hydroxylated naphtoquinones/antraquinones with pentafluoropyridine.

SpringerPlus

Beyki K, Haydari R, Maghsoodlou MT.
PMID: 26877908
Springerplus. 2016 Feb 01;5:110. doi: 10.1186/s40064-016-1708-5. eCollection 2016.

In this study, the reaction of pentafluoropyridine with hydroxylated naphtoquinones and hydroxylated antraquinones was investigated under basic conditions in DMF. One or two hydroxyl group in naphtoquinones and antraquinones react with pentafluoropyridine to give mono and di-tetrafluoropyridyl naphtoquinones/antraquinones. All...

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Beyki K, Haydari R, Maghsoodlou MT. Reaction of hydroxylated naphtoquinones/antraquinones with pentafluoropyridine. Springerplus. 2016;5:110doi: 10.1186/s40064-016-1708-5.
Beyki, K., Haydari, R., & Maghsoodlou, M. T. (2016). Reaction of hydroxylated naphtoquinones/antraquinones with pentafluoropyridine. SpringerPlus, 5110. https://doi.org/10.1186/s40064-016-1708-5
Beyki, Khalil, et al. "Reaction of hydroxylated naphtoquinones/antraquinones with pentafluoropyridine." SpringerPlus vol. 5 (2016): 110. doi: https://doi.org/10.1186/s40064-016-1708-5
Beyki K, Haydari R, Maghsoodlou MT. Reaction of hydroxylated naphtoquinones/antraquinones with pentafluoropyridine. Springerplus. 2016 Feb 01;5:110. doi: 10.1186/s40064-016-1708-5. eCollection 2016. PMID: 26877908; PMCID: PMC4735081.
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Dynamic 1H NMR study around the carbon-carbon single bond and partial carbon-carbon double bond in the two particular phosphorus ylides and in an enaminoester.

Magnetic resonance in chemistry : MRC

Habibi-Khorassani SM, Ebrahimi A, Maghsoodlou MT, Same-Salari S, Nasiri S, Ghasempour H.
PMID: 21387402
Magn Reson Chem. 2011 May;49(5):213-20. doi: 10.1002/mrc.2735. Epub 2011 Mar 09.

Herein, a series of separate dynamic (1)H NMR effects are reported at different temperatures within a particular enaminoester involving a phenanthridine. These effects are attributed to restricted rotation around the two single bonds such as carbon-carbon (H(a)-C-C-H(b)) and nitrogen-carbon...

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Habibi-Khorassani SM, Ebrahimi A, Maghsoodlou MT, et al. Dynamic 1H NMR study around the carbon-carbon single bond and partial carbon-carbon double bond in the two particular phosphorus ylides and in an enaminoester. Magn Reson Chem. 2011;49(5):213-20doi: 10.1002/mrc.2735.
Habibi-Khorassani, S. M., Ebrahimi, A., Maghsoodlou, M. T., Same-Salari, S., Nasiri, S., & Ghasempour, H. (2011). Dynamic 1H NMR study around the carbon-carbon single bond and partial carbon-carbon double bond in the two particular phosphorus ylides and in an enaminoester. Magnetic resonance in chemistry : MRC, 49(5), 213-20. https://doi.org/10.1002/mrc.2735
Habibi-Khorassani, Sayyed Mostafa, et al. "Dynamic 1H NMR study around the carbon-carbon single bond and partial carbon-carbon double bond in the two particular phosphorus ylides and in an enaminoester." Magnetic resonance in chemistry : MRC vol. 49,5 (2011): 213-20. doi: https://doi.org/10.1002/mrc.2735
Habibi-Khorassani SM, Ebrahimi A, Maghsoodlou MT, Same-Salari S, Nasiri S, Ghasempour H. Dynamic 1H NMR study around the carbon-carbon single bond and partial carbon-carbon double bond in the two particular phosphorus ylides and in an enaminoester. Magn Reson Chem. 2011 May;49(5):213-20. doi: 10.1002/mrc.2735. Epub 2011 Mar 09. PMID: 21387402.
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Establishing a new conductance stopped-flow apparatus to investigate the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene and methanol under a dry inert atmosphere.

The Analyst

Habibi Khorassani SM, Ebrahimi A, Maghsoodlou MT, Shahraki M, Price D.
PMID: 21359285
Analyst. 2011 Apr 21;136(8):1713-21. doi: 10.1039/c0an00817f. Epub 2011 Feb 25.

In the present work, for the first time, investigation of the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene (TCMP) and methanol was studied under a dry inert atmosphere by a newly constructed CSF apparatus by means of a further...

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Habibi Khorassani SM, Ebrahimi A, Maghsoodlou MT, et al. Establishing a new conductance stopped-flow apparatus to investigate the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene and methanol under a dry inert atmosphere. Analyst. 2011;136(8):1713-21doi: 10.1039/c0an00817f.
Habibi Khorassani, S. M., Ebrahimi, A., Maghsoodlou, M. T., Shahraki, M., & Price, D. (2011). Establishing a new conductance stopped-flow apparatus to investigate the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene and methanol under a dry inert atmosphere. The Analyst, 136(8), 1713-21. https://doi.org/10.1039/c0an00817f
Habibi Khorassani, Sayyed Mostafa, et al. "Establishing a new conductance stopped-flow apparatus to investigate the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene and methanol under a dry inert atmosphere." The Analyst vol. 136,8 (2011): 1713-21. doi: https://doi.org/10.1039/c0an00817f
Habibi Khorassani SM, Ebrahimi A, Maghsoodlou MT, Shahraki M, Price D. Establishing a new conductance stopped-flow apparatus to investigate the initial fast step of reaction between 1,1,1-trichloro-3-methyl-3-phospholene and methanol under a dry inert atmosphere. Analyst. 2011 Apr 21;136(8):1713-21. doi: 10.1039/c0an00817f. Epub 2011 Feb 25. PMID: 21359285.
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Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles.

SpringerPlus

Beyki K, Maghsoodlou MT, Heydari R.
PMID: 27933240
Springerplus. 2016 Nov 11;5(1):1961. doi: 10.1186/s40064-016-3398-4. eCollection 2016.

No abstract available.

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Beyki K, Maghsoodlou MT, Heydari R. Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles. Springerplus. 2016;5(1):1961doi: 10.1186/s40064-016-3398-4.
Beyki, K., Maghsoodlou, M. T., & Heydari, R. (2016). Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles. SpringerPlus, 5(1), 1961. https://doi.org/10.1186/s40064-016-3398-4
Beyki, Khalil, et al. "Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles." SpringerPlus vol. 5,1 (2016): 1961. doi: https://doi.org/10.1186/s40064-016-3398-4
Beyki K, Maghsoodlou MT, Heydari R. Synthesis of 2-tetrafluoropyridyl-4,5-disubstituted 1,2,3-triazoles. Springerplus. 2016 Nov 11;5(1):1961. doi: 10.1186/s40064-016-3398-4. eCollection 2016. PMID: 27933240; PMCID: PMC5106409.
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Synthesis of 2,3,5,6-tetrafluoro-pyridine derivatives from reaction of pentafluoropyridine with malononitrile, piperazine and tetrazole-5-thiol.

SpringerPlus

Beyki K, Haydari R, Maghsoodlou MT.
PMID: 26674807
Springerplus. 2015 Dec 04;4:757. doi: 10.1186/s40064-015-1495-4. eCollection 2015.

Some pentafluoropyridine derivatives have been synthesized by the reaction of pentafluoropyridine with appropriate C, S and N-nucleophile such as malononitrile, 1-methyl-tetrazole-5-thiol and piperazine. These reactions provided 4-substituted 2,3,5,6-tetrafluoropyridine derivatives in good yields. All the compounds were characterized using (1)H,...

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Beyki K, Haydari R, Maghsoodlou MT. Synthesis of 2,3,5,6-tetrafluoro-pyridine derivatives from reaction of pentafluoropyridine with malononitrile, piperazine and tetrazole-5-thiol. Springerplus. 2015;4:757doi: 10.1186/s40064-015-1495-4.
Beyki, K., Haydari, R., & Maghsoodlou, M. T. (2015). Synthesis of 2,3,5,6-tetrafluoro-pyridine derivatives from reaction of pentafluoropyridine with malononitrile, piperazine and tetrazole-5-thiol. SpringerPlus, 4757. https://doi.org/10.1186/s40064-015-1495-4
Beyki, Khalil, et al. "Synthesis of 2,3,5,6-tetrafluoro-pyridine derivatives from reaction of pentafluoropyridine with malononitrile, piperazine and tetrazole-5-thiol." SpringerPlus vol. 4 (2015): 757. doi: https://doi.org/10.1186/s40064-015-1495-4
Beyki K, Haydari R, Maghsoodlou MT. Synthesis of 2,3,5,6-tetrafluoro-pyridine derivatives from reaction of pentafluoropyridine with malononitrile, piperazine and tetrazole-5-thiol. Springerplus. 2015 Dec 04;4:757. doi: 10.1186/s40064-015-1495-4. eCollection 2015. PMID: 26674807; PMCID: PMC4670442.
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JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden.

International journal of hematology-oncology and stem cell research

Ferdowsi S, Ghaffari SH, Amirizadeh N, Azarkeivan A, Atarodi K, Faranoush M, Toogeh G, Shirkoohi R, Vaezi M, Maghsoodlu M, Alimoghaddam K, Ghavamzadeh A, Teimori Naghadeh H.
PMID: 27252806
Int J Hematol Oncol Stem Cell Res. 2016 Apr 01;10(2):70-8.

BACKGROUND: Myeloproliferative neoplasms (MPNs) are clonal malignant diseases that represent a group of conditions including polycythemia vera (PV), essential thrombocythemia (ET) and primary myelofibrosis (PMF). The aim of this study was to evaluate possible correlations between JAK2V617F allele burden...

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Ferdowsi S, Ghaffari SH, Amirizadeh N, et al. JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden. Int J Hematol Oncol Stem Cell Res. 2016;10(2):70-8
Ferdowsi, S., Ghaffari, S. H., Amirizadeh, N., Azarkeivan, A., Atarodi, K., Faranoush, M., Toogeh, G., Shirkoohi, R., Vaezi, M., Maghsoodlu, M., Alimoghaddam, K., Ghavamzadeh, A., & Teimori Naghadeh, H. (2016). JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden. International journal of hematology-oncology and stem cell research, 10(2), 70-8.
Ferdowsi, Shirin, et al. "JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden." International journal of hematology-oncology and stem cell research vol. 10,2 (2016): 70-8.
Ferdowsi S, Ghaffari SH, Amirizadeh N, Azarkeivan A, Atarodi K, Faranoush M, Toogeh G, Shirkoohi R, Vaezi M, Maghsoodlu M, Alimoghaddam K, Ghavamzadeh A, Teimori Naghadeh H. JAK2V617F Allele Burden Measurement in Peripheral Blood of Iranian Patients with Myeloproliferative Neoplasms and Effect of Hydroxyurea on JAK2V617F Allele Burden. Int J Hematol Oncol Stem Cell Res. 2016 Apr 01;10(2):70-8. PMID: 27252806; PMCID: PMC4888151.
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Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran.

Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis

Bakhshandeh Z, Amirizadeh N, Maghsoodlu M, Oodi A, Naghi A, Khazaeli AA, Azarkeivan A.
PMID: 33839013
Transfus Apher Sci. 2021 Jun;60(3):103124. doi: 10.1016/j.transci.2021.103124. Epub 2021 Apr 02.

BACKGROUND: Rhesus (Rh) blood group system is clinically the most significant protein-based grouping system. The Rh system is of vital importance in blood transfusion, and incompatibility between the donor and recipient leads to alloimmunization. Alloimmunization is commonly seen in...

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Bakhshandeh Z, Amirizadeh N, Maghsoodlu M, et al. Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran. Transfus Apher Sci. 2021;60(3):103124doi: 10.1016/j.transci.2021.103124.
Bakhshandeh, Z., Amirizadeh, N., Maghsoodlu, M., Oodi, A., Naghi, A., Khazaeli, A. A., & Azarkeivan, A. (2021). Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran. Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis, 60(3), 103124. https://doi.org/10.1016/j.transci.2021.103124
Bakhshandeh, Zahra, et al. "Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran." Transfusion and apheresis science : official journal of the World Apheresis Association : official journal of the European Society for Haemapheresis vol. 60,3 (2021): 103124. doi: https://doi.org/10.1016/j.transci.2021.103124
Bakhshandeh Z, Amirizadeh N, Maghsoodlu M, Oodi A, Naghi A, Khazaeli AA, Azarkeivan A. Developing a databank for multiple transfusion patients: Rh antigen and phenotype distribution among 3000 regular blood donors in Iran. Transfus Apher Sci. 2021 Jun;60(3):103124. doi: 10.1016/j.transci.2021.103124. Epub 2021 Apr 02. PMID: 33839013.
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Reaction of hydroxyl-quinoline with pentafluoropyridin.

SpringerPlus

Beyki K, Maghsoodlou MT, Heydari R.
PMID: 27933252
Springerplus. 2016 Nov 22;5(1):1996. doi: 10.1186/s40064-016-3410-z. eCollection 2016.

Reaction of pentafluoropyridine with 2 or 8-hydroxyl-quinoline under basic conditions in acetonitrile gives 4-oxy quinoline 2,3,5,6-tetrafluoropyridine derivatives in good yields. All the compounds were characterized using

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Beyki K, Maghsoodlou MT, Heydari R. Reaction of hydroxyl-quinoline with pentafluoropyridin. Springerplus. 2016;5(1):1996doi: 10.1186/s40064-016-3410-z.
Beyki, K., Maghsoodlou, M. T., & Heydari, R. (2016). Reaction of hydroxyl-quinoline with pentafluoropyridin. SpringerPlus, 5(1), 1996. https://doi.org/10.1186/s40064-016-3410-z
Beyki, Khalil, et al. "Reaction of hydroxyl-quinoline with pentafluoropyridin." SpringerPlus vol. 5,1 (2016): 1996. doi: https://doi.org/10.1186/s40064-016-3410-z
Beyki K, Maghsoodlou MT, Heydari R. Reaction of hydroxyl-quinoline with pentafluoropyridin. Springerplus. 2016 Nov 22;5(1):1996. doi: 10.1186/s40064-016-3410-z. eCollection 2016. PMID: 27933252; PMCID: PMC5118374.
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Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit.

Avicenna journal of phytomedicine

Nikbin M, Kazemipour N, Maghsoodlou MT, Valizadeh J, Sepehrimanesh M, Davarimanesh A.
PMID: 25050316
Avicenna J Phytomed. 2014 May;4(3):182-90.

OBJECTIVE: Scutellaria luteo-caerulea Bornm. & Snit. is one of the species of genus Scutellaria, within the family of the Lamiaceae, that is used for immune system stimulation and antibacterial effects in traditional medicine in Iran. The aims of this...

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Nikbin M, Kazemipour N, Maghsoodlou MT, et al. Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit. Avicenna J Phytomed. 2014;4(3):182-90
Nikbin, M., Kazemipour, N., Maghsoodlou, M. T., Valizadeh, J., Sepehrimanesh, M., & Davarimanesh, A. (2014). Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit. Avicenna journal of phytomedicine, 4(3), 182-90.
Nikbin, Mohammad, et al. "Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit." Avicenna journal of phytomedicine vol. 4,3 (2014): 182-90.
Nikbin M, Kazemipour N, Maghsoodlou MT, Valizadeh J, Sepehrimanesh M, Davarimanesh A. Mineral elements and essential oil contents of Scutellaria luteo-caerulea Bornm. & Snit. Avicenna J Phytomed. 2014 May;4(3):182-90. PMID: 25050316; PMCID: PMC4104630.
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Bone Regeneration Using Bio-Nanocomposite Tissue Reinforced with Bioactive Nanoparticles for Femoral Defect Applications in Medicine.

Avicenna journal of medical biotechnology

Maghsoudlou MA, Nassireslami E, Saber-Samandari S, Khandan A.
PMID: 32431790
Avicenna J Med Biotechnol. 2020 Apr-Jun;12(2):68-76.

BACKGROUND: In recent years, the method of constructing and evaluating the properties of polymer nanocomposite and bioactive ceramics in tissue engineering such as biocompatible scaffolds was studied by some researchers.METHODS: In this study, the bio-nanocomposite scaffolds of Chitosan (CS)-Hydroxyapatite...

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Maghsoudlou MA, Nassireslami E, Saber-Samandari S, et al. Bone Regeneration Using Bio-Nanocomposite Tissue Reinforced with Bioactive Nanoparticles for Femoral Defect Applications in Medicine. Avicenna J Med Biotechnol. 2020;12(2):68-76
Maghsoudlou, M. A., Nassireslami, E., Saber-Samandari, S., & Khandan, A. (2020). Bone Regeneration Using Bio-Nanocomposite Tissue Reinforced with Bioactive Nanoparticles for Femoral Defect Applications in Medicine. Avicenna journal of medical biotechnology, 12(2), 68-76.
Maghsoudlou, Mohammad Ali, et al. "Bone Regeneration Using Bio-Nanocomposite Tissue Reinforced with Bioactive Nanoparticles for Femoral Defect Applications in Medicine." Avicenna journal of medical biotechnology vol. 12,2 (2020): 68-76.
Maghsoudlou MA, Nassireslami E, Saber-Samandari S, Khandan A. Bone Regeneration Using Bio-Nanocomposite Tissue Reinforced with Bioactive Nanoparticles for Femoral Defect Applications in Medicine. Avicenna J Med Biotechnol. 2020 Apr-Jun;12(2):68-76. PMID: 32431790; PMCID: PMC7229459.
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Essential oil composition of Eucalyptus microtheca and Eucalyptus viminalis.

Avicenna journal of phytomedicine

Maghsoodlou MT, Kazemipoor N, Valizadeh J, Falak Nezhad Seifi M, Rahneshan N.
PMID: 26693411
Avicenna J Phytomed. 2015 Nov-Dec;5(6):540-52.

OBJECTIVE: Eucalyptus (Fam. Myrtaceae) is a medicinal plant and various Eucalyptus species possess potent pharmacological actions against diabetes, hepatotoxicity, and inflammation. This study aims to investigate essential oil composition from leaves and flowers of E. microtheca and E. viminalis...

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Maghsoodlou MT, Kazemipoor N, Valizadeh J, et al. Essential oil composition of Eucalyptus microtheca and Eucalyptus viminalis. Avicenna J Phytomed. 2015;5(6):540-52
Maghsoodlou, M. T., Kazemipoor, N., Valizadeh, J., Falak Nezhad Seifi, M., & Rahneshan, N. (2015). Essential oil composition of Eucalyptus microtheca and Eucalyptus viminalis. Avicenna journal of phytomedicine, 5(6), 540-52.
Maghsoodlou, Malek Taher, et al. "Essential oil composition of Eucalyptus microtheca and Eucalyptus viminalis." Avicenna journal of phytomedicine vol. 5,6 (2015): 540-52.
Maghsoodlou MT, Kazemipoor N, Valizadeh J, Falak Nezhad Seifi M, Rahneshan N. Essential oil composition of Eucalyptus microtheca and Eucalyptus viminalis. Avicenna J Phytomed. 2015 Nov-Dec;5(6):540-52. PMID: 26693411; PMCID: PMC4678499.
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