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Biomarkers of cancer angioprevention for clinical studies.

Ecancermedicalscience

Albini A, Bertolini F, Bassani B, Bruno A, Gallo C, Caraffi SG, Maramotti S, Noonan DM.
PMID: 26635904
Ecancermedicalscience. 2015 Nov 24;9:600. doi: 10.3332/ecancer.2015.600. eCollection 2015.

With the great advances made in the treatment and prevention of infectious diseases over the last century, chronic degenerative diseases-cardiovascular, cerebrovascular, and cancer-represent the major causes of death in the developed world. Although massive efforts and investments have been...

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Albini A, Bertolini F, Bassani B, et al. Biomarkers of cancer angioprevention for clinical studies. Ecancermedicalscience. 2015;9:600doi: 10.3332/ecancer.2015.600.
Albini, A., Bertolini, F., Bassani, B., Bruno, A., Gallo, C., Caraffi, S. G., Maramotti, S., & Noonan, D. M. (2015). Biomarkers of cancer angioprevention for clinical studies. Ecancermedicalscience, 9600. https://doi.org/10.3332/ecancer.2015.600
Albini, Adriana, et al. "Biomarkers of cancer angioprevention for clinical studies." Ecancermedicalscience vol. 9 (2015): 600. doi: https://doi.org/10.3332/ecancer.2015.600
Albini A, Bertolini F, Bassani B, Bruno A, Gallo C, Caraffi SG, Maramotti S, Noonan DM. Biomarkers of cancer angioprevention for clinical studies. Ecancermedicalscience. 2015 Nov 24;9:600. doi: 10.3332/ecancer.2015.600. eCollection 2015. PMID: 26635904; PMCID: PMC4664506.
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Metals as Catalysts during the Formation and Decomposition of Chlorinated Dioxins and Furans in Incineration Processes.

Journal of the Air & Waste Management Association (1995)

Olie K, Addink R, Schoonenboom M.
PMID: 28081422
J Air Waste Manag Assoc. 1998 Feb;48(2):101-105. doi: 10.1080/10473289.1998.10463656.

Polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) are found on fly ash and in flue gas of municipal waste incinerators. Municipal waste incinerators seem to be the most important source for PCDDs and PCDFs emitted into the air during...

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Olie K, Addink R, Schoonenboom M. Metals as Catalysts during the Formation and Decomposition of Chlorinated Dioxins and Furans in Incineration Processes. J Air Waste Manag Assoc. 1998;48(2):101-105doi: 10.1080/10473289.1998.10463656.
Olie, K., Addink, R., & Schoonenboom, M. (1998). Metals as Catalysts during the Formation and Decomposition of Chlorinated Dioxins and Furans in Incineration Processes. Journal of the Air & Waste Management Association (1995), 48(2), 101-105. https://doi.org/10.1080/10473289.1998.10463656
Olie, Kees, et al. "Metals as Catalysts during the Formation and Decomposition of Chlorinated Dioxins and Furans in Incineration Processes." Journal of the Air & Waste Management Association (1995) vol. 48,2 (1998): 101-105. doi: https://doi.org/10.1080/10473289.1998.10463656
Olie K, Addink R, Schoonenboom M. Metals as Catalysts during the Formation and Decomposition of Chlorinated Dioxins and Furans in Incineration Processes. J Air Waste Manag Assoc. 1998 Feb;48(2):101-105. doi: 10.1080/10473289.1998.10463656. PMID: 28081422.
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On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes.

The Journal of organic chemistry

Raviola C, Chiesa F, Protti S, Albini A, Fagnoni M.
PMID: 27383725
J Org Chem. 2016 Aug 05;81(15):6336-42. doi: 10.1021/acs.joc.6b00978. Epub 2016 Jul 20.

2-Chloro-, 2-bromo-, and 2-iodothiophenes undergo photochemical dehalogenation via the triplet state. In the presence of suitable π-bond nucleophiles, thienylation occurs with modest yield from chloro and bromo derivatives (via photogenerated triplet 2-thienyl cation). Specific trapping by using oxygen along...

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Raviola C, Chiesa F, Protti S, et al. On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes. J Org Chem. 2016;81(15):6336-42doi: 10.1021/acs.joc.6b00978.
Raviola, C., Chiesa, F., Protti, S., Albini, A., & Fagnoni, M. (2016). On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes. The Journal of organic chemistry, 81(15), 6336-42. https://doi.org/10.1021/acs.joc.6b00978
Raviola, Carlotta, et al. "On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes." The Journal of organic chemistry vol. 81,15 (2016): 6336-42. doi: https://doi.org/10.1021/acs.joc.6b00978
Raviola C, Chiesa F, Protti S, Albini A, Fagnoni M. On the Route to the Photogeneration of Heteroaryl Cations. The Case of Halothiophenes. J Org Chem. 2016 Aug 05;81(15):6336-42. doi: 10.1021/acs.joc.6b00978. Epub 2016 Jul 20. PMID: 27383725.
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Cationic arylation through photo(sensitised) decomposition of diazonium salts. Chemoselectivity of triplet phenyl cations.

Chemical communications (Cambridge, England)

Milanesi S, Fagnoni M, Albini A.
PMID: 12585398
Chem Commun (Camb). 2003 Jan 21;(2):216-7. doi: 10.1039/b210243a.

The photodediazoniation of some 4-X-phenyldiazonium tetrafluoborates in MeCN leads to the singlet phenyl cations (X = H, tert-butyl, NMe2, CN), which add to the solvent yielding the corresponding acetanilides. Triplet sensitisation, however, leads to the triplet phenyl cation, which...

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Milanesi S, Fagnoni M, Albini A. Cationic arylation through photo(sensitised) decomposition of diazonium salts. Chemoselectivity of triplet phenyl cations. Chem Commun (Camb). 2003;(2):216-7doi: 10.1039/b210243a.
Milanesi, S., Fagnoni, M., & Albini, A. (2003). Cationic arylation through photo(sensitised) decomposition of diazonium salts. Chemoselectivity of triplet phenyl cations. Chemical communications (Cambridge, England), (2), 216-7. https://doi.org/10.1039/b210243a
Milanesi, Silvia, et al. "Cationic arylation through photo(sensitised) decomposition of diazonium salts. Chemoselectivity of triplet phenyl cations." Chemical communications (Cambridge, England) vol. ,2 (2003): 216-7. doi: https://doi.org/10.1039/b210243a
Milanesi S, Fagnoni M, Albini A. Cationic arylation through photo(sensitised) decomposition of diazonium salts. Chemoselectivity of triplet phenyl cations. Chem Commun (Camb). 2003 Jan 21;(2):216-7. doi: 10.1039/b210243a. PMID: 12585398.
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(Sensitized) photolysis of diazonium salts as a mild general method for the generation of aryl cations. Chemoselectivity of the singlet and triplet 4-substituted phenyl cations.

The Journal of organic chemistry

Milanesi S, Fagnoni M, Albini A.
PMID: 15651808
J Org Chem. 2005 Jan 21;70(2):603-10. doi: 10.1021/jo048413w.

The photolysis of a series of 4-X-benzenediazonium tetrafluoroborates is studied in MeCN. Loss of nitrogen occurs from the singlet excited state with X=H, t-Bu, and NMe2 and leads to the singlet aryl cation. This adds to the solvent yielding...

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Milanesi S, Fagnoni M, Albini A. (Sensitized) photolysis of diazonium salts as a mild general method for the generation of aryl cations. Chemoselectivity of the singlet and triplet 4-substituted phenyl cations. J Org Chem. 2005;70(2):603-10doi: 10.1021/jo048413w.
Milanesi, S., Fagnoni, M., & Albini, A. (2005). (Sensitized) photolysis of diazonium salts as a mild general method for the generation of aryl cations. Chemoselectivity of the singlet and triplet 4-substituted phenyl cations. The Journal of organic chemistry, 70(2), 603-10. https://doi.org/10.1021/jo048413w
Milanesi, Silvia, et al. "(Sensitized) photolysis of diazonium salts as a mild general method for the generation of aryl cations. Chemoselectivity of the singlet and triplet 4-substituted phenyl cations." The Journal of organic chemistry vol. 70,2 (2005): 603-10. doi: https://doi.org/10.1021/jo048413w
Milanesi S, Fagnoni M, Albini A. (Sensitized) photolysis of diazonium salts as a mild general method for the generation of aryl cations. Chemoselectivity of the singlet and triplet 4-substituted phenyl cations. J Org Chem. 2005 Jan 21;70(2):603-10. doi: 10.1021/jo048413w. PMID: 15651808.
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Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes.

Journal of the American Chemical Society

Carra C, Bally T, Albini A.
PMID: 15826193
J Am Chem Soc. 2005 Apr 20;127(15):5552-62. doi: 10.1021/ja043988w.

The chemistry of 2-(1-pyrazolyl)- (2a) and 2-[1-(3,5-dimethylpyrazolyl]phenylnitrene (2b) has been studied in EtOH solution at room temperature, in EtOH glasses at 90 K, and in Ar matrices at 12 K. These nitrenes were chosen as suitable models for clarifying...

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Carra C, Bally T, Albini A. Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes. J Am Chem Soc. 2005;127(15):5552-62doi: 10.1021/ja043988w.
Carra, C., Bally, T., & Albini, A. (2005). Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes. Journal of the American Chemical Society, 127(15), 5552-62. https://doi.org/10.1021/ja043988w
Carra, Claudio, et al. "Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes." Journal of the American Chemical Society vol. 127,15 (2005): 5552-62. doi: https://doi.org/10.1021/ja043988w
Carra C, Bally T, Albini A. Role of conformation and electronic structure in the chemistry of ground and excited state o-pyrazolylphenylnitrenes. J Am Chem Soc. 2005 Apr 20;127(15):5552-62. doi: 10.1021/ja043988w. PMID: 15826193.
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Photo-cross-coupling reaction of electron-rich aryl chlorides and aryl esters with alkynes: a metal-free alkynylation.

Angewandte Chemie (International ed. in English)

Protti S, Fagnoni M, Albini A.
PMID: 16086352
Angew Chem Int Ed Engl. 2005 Sep 05;44(35):5675-8. doi: 10.1002/anie.200501541.

No abstract available.

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Protti S, Fagnoni M, Albini A. Photo-cross-coupling reaction of electron-rich aryl chlorides and aryl esters with alkynes: a metal-free alkynylation. Angew Chem Int Ed Engl. 2005;44(35):5675-8doi: 10.1002/anie.200501541.
Protti, S., Fagnoni, M., & Albini, A. (2005). Photo-cross-coupling reaction of electron-rich aryl chlorides and aryl esters with alkynes: a metal-free alkynylation. Angewandte Chemie (International ed. in English), 44(35), 5675-8. https://doi.org/10.1002/anie.200501541
Protti, Stefano, et al. "Photo-cross-coupling reaction of electron-rich aryl chlorides and aryl esters with alkynes: a metal-free alkynylation." Angewandte Chemie (International ed. in English) vol. 44,35 (2005): 5675-8. doi: https://doi.org/10.1002/anie.200501541
Protti S, Fagnoni M, Albini A. Photo-cross-coupling reaction of electron-rich aryl chlorides and aryl esters with alkynes: a metal-free alkynylation. Angew Chem Int Ed Engl. 2005 Sep 05;44(35):5675-8. doi: 10.1002/anie.200501541. PMID: 16086352.
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Correlation of transverse and rotational diffusion coefficient: a probe of chemical composition in hydrocarbon oils.

The journal of physical chemistry. A

Mutina AR, Hürlimann MD.
PMID: 18335907
J Phys Chem A. 2008 Apr 17;112(15):3291-301. doi: 10.1021/jp710254d. Epub 2008 Mar 12.

Measurements of relaxation time and diffusion coefficient by nuclear magnetic resonance are well-established techniques to study molecular motions in fluids. Diffusion measurements sense the translational diffusion coefficients of the molecules, whereas relaxation times measured at low magnetic fields probe...

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Mutina AR, Hürlimann MD. Correlation of transverse and rotational diffusion coefficient: a probe of chemical composition in hydrocarbon oils. J Phys Chem A. 2008;112(15):3291-301doi: 10.1021/jp710254d.
Mutina, A. R., & Hürlimann, M. D. (2008). Correlation of transverse and rotational diffusion coefficient: a probe of chemical composition in hydrocarbon oils. The journal of physical chemistry. A, 112(15), 3291-301. https://doi.org/10.1021/jp710254d
Mutina, Albina R, and Hürlimann, Martin D. "Correlation of transverse and rotational diffusion coefficient: a probe of chemical composition in hydrocarbon oils." The journal of physical chemistry. A vol. 112,15 (2008): 3291-301. doi: https://doi.org/10.1021/jp710254d
Mutina AR, Hürlimann MD. Correlation of transverse and rotational diffusion coefficient: a probe of chemical composition in hydrocarbon oils. J Phys Chem A. 2008 Apr 17;112(15):3291-301. doi: 10.1021/jp710254d. Epub 2008 Mar 12. PMID: 18335907.
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Copy number variation at 1q21.1 results in a spectrum of developmental abnormalities.

Clinical genetics

Aldinger KA.
PMID: 19459881
Clin Genet. 2009 May;75(5):425-7. doi: 10.1111/j.1399-0004.2009.01186_2.x.

No abstract available.

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Aldinger KA. Copy number variation at 1q21.1 results in a spectrum of developmental abnormalities. Clin Genet. 2009;75(5):425-7doi: 10.1111/j.1399-0004.2009.01186_2.x.
Aldinger, K. A. (2009). Copy number variation at 1q21.1 results in a spectrum of developmental abnormalities. Clinical genetics, 75(5), 425-7. https://doi.org/10.1111/j.1399-0004.2009.01186_2.x
Aldinger, Kimbery A. "Copy number variation at 1q21.1 results in a spectrum of developmental abnormalities." Clinical genetics vol. 75,5 (2009): 425-7. doi: https://doi.org/10.1111/j.1399-0004.2009.01186_2.x
Aldinger KA. Copy number variation at 1q21.1 results in a spectrum of developmental abnormalities. Clin Genet. 2009 May;75(5):425-7. doi: 10.1111/j.1399-0004.2009.01186_2.x. PMID: 19459881.
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Photocatalysis. A multi-faceted concept for green chemistry.

Chemical Society reviews

Ravelli D, Dondi D, Fagnoni M, Albini A.
PMID: 19551179
Chem Soc Rev. 2009 Jul;38(7):1999-2011. doi: 10.1039/b714786b. Epub 2009 Apr 21.

Photocatalysis (by semiconductors, molecules and ions) is used in such diverse applications as water hydrolysis for producing hydrogen as fuel, organic synthesis and the recovery of polluted effluents. This tutorial review discusses the common principles of such applications and...

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Ravelli D, Dondi D, Fagnoni M, et al. Photocatalysis. A multi-faceted concept for green chemistry. Chem Soc Rev. 2009;38(7):1999-2011doi: 10.1039/b714786b.
Ravelli, D., Dondi, D., Fagnoni, M., & Albini, A. (2009). Photocatalysis. A multi-faceted concept for green chemistry. Chemical Society reviews, 38(7), 1999-2011. https://doi.org/10.1039/b714786b
Ravelli, Davide, et al. "Photocatalysis. A multi-faceted concept for green chemistry." Chemical Society reviews vol. 38,7 (2009): 1999-2011. doi: https://doi.org/10.1039/b714786b
Ravelli D, Dondi D, Fagnoni M, Albini A. Photocatalysis. A multi-faceted concept for green chemistry. Chem Soc Rev. 2009 Jul;38(7):1999-2011. doi: 10.1039/b714786b. Epub 2009 Apr 21. PMID: 19551179.
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Photoinduced three-component reaction: a convenient access to 3-arylacetals or 3-arylketals.

Organic letters

Lazzaroni S, Protti S, Fagnoni M, Albini A.
PMID: 19072131
Org Lett. 2009 Jan 15;11(2):349-52. doi: 10.1021/ol802560t.

A mild and versatile method for the photoinduced three-component synthesis of 3-arylacetals and ketals is presented. Desired targets are smoothly obtained by irradiating aromatic halides or esters in alcohols, in the presence of vinyl ethers.

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Lazzaroni S, Protti S, Fagnoni M, et al. Photoinduced three-component reaction: a convenient access to 3-arylacetals or 3-arylketals. Org Lett. 2009;11(2):349-52doi: 10.1021/ol802560t.
Lazzaroni, S., Protti, S., Fagnoni, M., & Albini, A. (2009). Photoinduced three-component reaction: a convenient access to 3-arylacetals or 3-arylketals. Organic letters, 11(2), 349-52. https://doi.org/10.1021/ol802560t
Lazzaroni, Simone, et al. "Photoinduced three-component reaction: a convenient access to 3-arylacetals or 3-arylketals." Organic letters vol. 11,2 (2009): 349-52. doi: https://doi.org/10.1021/ol802560t
Lazzaroni S, Protti S, Fagnoni M, Albini A. Photoinduced three-component reaction: a convenient access to 3-arylacetals or 3-arylketals. Org Lett. 2009 Jan 15;11(2):349-52. doi: 10.1021/ol802560t. PMID: 19072131.
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Intramolecular electron transfer in the photochemistry of some nitrophenyldihydropyridines.

The Journal of organic chemistry

Fasani E, Fagnoni M, Dondi D, Albini A.
PMID: 16496991
J Org Chem. 2006 Mar 03;71(5):2037-45. doi: 10.1021/jo052463z.

4-Phenyl-1,4-dihydropyridine-3,5-dicarboxylates contain two pi chromophores separated by an sp3 carbon. The lowest singlet is localized on the dihydropyridine moiety (1PyH2-Ph) and emits a blue fluorescence (with close to unitary efficiency in glass at 77 K). In 3-nitrophenyl derivatives (PyH2-PhNO2,...

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Fasani E, Fagnoni M, Dondi D, et al. Intramolecular electron transfer in the photochemistry of some nitrophenyldihydropyridines. J Org Chem. 2006;71(5):2037-45doi: 10.1021/jo052463z.
Fasani, E., Fagnoni, M., Dondi, D., & Albini, A. (2006). Intramolecular electron transfer in the photochemistry of some nitrophenyldihydropyridines. The Journal of organic chemistry, 71(5), 2037-45. https://doi.org/10.1021/jo052463z
Fasani, Elisa, et al. "Intramolecular electron transfer in the photochemistry of some nitrophenyldihydropyridines." The Journal of organic chemistry vol. 71,5 (2006): 2037-45. doi: https://doi.org/10.1021/jo052463z
Fasani E, Fagnoni M, Dondi D, Albini A. Intramolecular electron transfer in the photochemistry of some nitrophenyldihydropyridines. J Org Chem. 2006 Mar 03;71(5):2037-45. doi: 10.1021/jo052463z. PMID: 16496991.
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Showing 1 to 12 of 318 entries