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Cocrystals of 1,4-diethynylbenzene with 1,3-diacetylbenzene and benzene-1,4-dicarbaldehyde exhibiting strong nonconventional alkyne-carbonyl C-H...O hydrogen bonds between the components.

Acta crystallographica. Section C, Structural chemistry

Bosch E.
PMID: 27703122
Acta Crystallogr C Struct Chem. 2016 Oct 01;72:748-752. doi: 10.1107/S2053229616014972. Epub 2016 Sep 26.

Weak interactions between organic molecules are important in solid-state structures where the sum of the weaker interactions support the overall three-dimensional crystal structure. The sp-C-H...N hydrogen-bonding interaction is strong enough to promote the deliberate cocrystallization of a series of...

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Bosch E. Cocrystals of 1,4-diethynylbenzene with 1,3-diacetylbenzene and benzene-1,4-dicarbaldehyde exhibiting strong nonconventional alkyne-carbonyl C-H...O hydrogen bonds between the components. Acta Crystallogr C Struct Chem. 2016;72:748-752doi: 10.1107/S2053229616014972.
Bosch, E. (2016). Cocrystals of 1,4-diethynylbenzene with 1,3-diacetylbenzene and benzene-1,4-dicarbaldehyde exhibiting strong nonconventional alkyne-carbonyl C-H...O hydrogen bonds between the components. Acta crystallographica. Section C, Structural chemistry, 72748-752. https://doi.org/10.1107/S2053229616014972
Bosch, Eric. "Cocrystals of 1,4-diethynylbenzene with 1,3-diacetylbenzene and benzene-1,4-dicarbaldehyde exhibiting strong nonconventional alkyne-carbonyl C-H...O hydrogen bonds between the components." Acta crystallographica. Section C, Structural chemistry vol. 72 (2016): 748-752. doi: https://doi.org/10.1107/S2053229616014972
Bosch E. Cocrystals of 1,4-diethynylbenzene with 1,3-diacetylbenzene and benzene-1,4-dicarbaldehyde exhibiting strong nonconventional alkyne-carbonyl C-H...O hydrogen bonds between the components. Acta Crystallogr C Struct Chem. 2016 Oct 01;72:748-752. doi: 10.1107/S2053229616014972. Epub 2016 Sep 26. PMID: 27703122.
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Cognitive performance before and after the onset of subjective cognitive decline in old age.

Alzheimer's & dementia (Amsterdam, Netherlands)

Koppara A, Wagner M, Lange C, Ernst A, Wiese B, König HH, Brettschneider C, Riedel-Heller S, Luppa M, Weyerer S, Werle J, Bickel H, Mösch E, Pentzek M, Fuchs A, Wolfsgruber S, Beauducel A, Scherer M, Maier W, Jessen F.
PMID: 27239504
Alzheimers Dement (Amst). 2015 May 02;1(2):194-205. doi: 10.1016/j.dadm.2015.02.005. eCollection 2015 Jun.

BACKGROUND: Our objectives were (1) to test the association between the report of subjective cognitive decline (SCD) and prospective objective cognitive performance in high age individuals and (2) to study the course of longitudinal cognitive performance before and after...

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Koppara A, Wagner M, Lange C, et al. Cognitive performance before and after the onset of subjective cognitive decline in old age. Alzheimers Dement (Amst). 2015;1(2):194-205doi: 10.1016/j.dadm.2015.02.005.
Koppara, A., Wagner, M., Lange, C., Ernst, A., Wiese, B., König, H. H., Brettschneider, C., Riedel-Heller, S., Luppa, M., Weyerer, S., Werle, J., Bickel, H., Mösch, E., Pentzek, M., Fuchs, A., Wolfsgruber, S., Beauducel, A., Scherer, M., Maier, W., & Jessen, F. (2015). Cognitive performance before and after the onset of subjective cognitive decline in old age. Alzheimer's & dementia (Amsterdam, Netherlands), 1(2), 194-205. https://doi.org/10.1016/j.dadm.2015.02.005
Koppara, Alexander, et al. "Cognitive performance before and after the onset of subjective cognitive decline in old age." Alzheimer's & dementia (Amsterdam, Netherlands) vol. 1,2 (2015): 194-205. doi: https://doi.org/10.1016/j.dadm.2015.02.005
Koppara A, Wagner M, Lange C, Ernst A, Wiese B, König HH, Brettschneider C, Riedel-Heller S, Luppa M, Weyerer S, Werle J, Bickel H, Mösch E, Pentzek M, Fuchs A, Wolfsgruber S, Beauducel A, Scherer M, Maier W, Jessen F. Cognitive performance before and after the onset of subjective cognitive decline in old age. Alzheimers Dement (Amst). 2015 May 02;1(2):194-205. doi: 10.1016/j.dadm.2015.02.005. eCollection 2015 Jun. PMID: 27239504; PMCID: PMC4876897.
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Chromatographic Hydrophobicity Index (CHI).

Advances in chromatography

Rosés M, Bosch E, Ràfols C, Fuguet E.
PMID: 26437516
Adv Chromatogr. 2012;50:377-414. doi: 10.1201/b11636-9.

No abstract available.

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Rosés M, Bosch E, Ràfols C, et al. Chromatographic Hydrophobicity Index (CHI). Adv Chromatogr. 2012;50:377-414doi: 10.1201/b11636-9.
Rosés, M., Bosch, E., Ràfols, C., & Fuguet, E. (2012). Chromatographic Hydrophobicity Index (CHI). Advances in chromatography, 50377-414. https://doi.org/10.1201/b11636-9
Rosés, Martí, et al. "Chromatographic Hydrophobicity Index (CHI)." Advances in chromatography vol. 50 (2012): 377-414. doi: https://doi.org/10.1201/b11636-9
Rosés M, Bosch E, Ràfols C, Fuguet E. Chromatographic Hydrophobicity Index (CHI). Adv Chromatogr. 2012;50:377-414. doi: 10.1201/b11636-9. PMID: 26437516.
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Sitagliptin ameliorates oxidative stress in experimental diabetic nephropathy by diminishing the miR-200a/Keap-1/Nrf2 antioxidant pathway.

Diabetes, metabolic syndrome and obesity : targets and therapy

Civantos E, Bosch E, Ramirez E, Zhenyukh O, Egido J, Lorenzo O, Mas S.
PMID: 28652790
Diabetes Metab Syndr Obes. 2017 Jun 07;10:207-222. doi: 10.2147/DMSO.S132537. eCollection 2017.

BACKGROUND: Sitagliptin, a dipeptidyl peptidase-4 (DPP-4) inhibitor used in type 2 diabetes therapy, has demonstrated protective effects in diabetic chronic kidney disease, in part due to its pleiotropic actions. However, its potential direct effects on the kidney are still...

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Civantos E, Bosch E, Ramirez E, et al. Sitagliptin ameliorates oxidative stress in experimental diabetic nephropathy by diminishing the miR-200a/Keap-1/Nrf2 antioxidant pathway. Diabetes Metab Syndr Obes. 2017;10:207-222doi: 10.2147/DMSO.S132537.
Civantos, E., Bosch, E., Ramirez, E., Zhenyukh, O., Egido, J., Lorenzo, O., & Mas, S. (2017). Sitagliptin ameliorates oxidative stress in experimental diabetic nephropathy by diminishing the miR-200a/Keap-1/Nrf2 antioxidant pathway. Diabetes, metabolic syndrome and obesity : targets and therapy, 10207-222. https://doi.org/10.2147/DMSO.S132537
Civantos, Esther, et al. "Sitagliptin ameliorates oxidative stress in experimental diabetic nephropathy by diminishing the miR-200a/Keap-1/Nrf2 antioxidant pathway." Diabetes, metabolic syndrome and obesity : targets and therapy vol. 10 (2017): 207-222. doi: https://doi.org/10.2147/DMSO.S132537
Civantos E, Bosch E, Ramirez E, Zhenyukh O, Egido J, Lorenzo O, Mas S. Sitagliptin ameliorates oxidative stress in experimental diabetic nephropathy by diminishing the miR-200a/Keap-1/Nrf2 antioxidant pathway. Diabetes Metab Syndr Obes. 2017 Jun 07;10:207-222. doi: 10.2147/DMSO.S132537. eCollection 2017. PMID: 28652790; PMCID: PMC5473486.
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Prefrontal inputs to the amygdala instruct fear extinction memory formation.

Science advances

Bukalo O, Pinard CR, Silverstein S, Brehm C, Hartley ND, Whittle N, Colacicco G, Busch E, Patel S, Singewald N, Holmes A.
PMID: 26504902
Sci Adv. 2015 Jul;1(6). doi: 10.1126/sciadv.1500251. Epub 2015 Jul 31.

Persistent anxiety after a psychological trauma is a hallmark of many anxiety disorders. However, the neural circuits mediating the extinction of traumatic fear memories remain incompletely understood. We show that selective, in vivo stimulation of the ventromedial prefrontal cortex...

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Bukalo O, Pinard CR, Silverstein S, et al. Prefrontal inputs to the amygdala instruct fear extinction memory formation. Sci Adv. 2015;1(6)doi: 10.1126/sciadv.1500251.
Bukalo, O., Pinard, C. R., Silverstein, S., Brehm, C., Hartley, N. D., Whittle, N., Colacicco, G., Busch, E., Patel, S., Singewald, N., & Holmes, A. (2015). Prefrontal inputs to the amygdala instruct fear extinction memory formation. Science advances, 1(6), . https://doi.org/10.1126/sciadv.1500251
Bukalo, Olena, et al. "Prefrontal inputs to the amygdala instruct fear extinction memory formation." Science advances vol. 1,6 (2015). doi: https://doi.org/10.1126/sciadv.1500251
Bukalo O, Pinard CR, Silverstein S, Brehm C, Hartley ND, Whittle N, Colacicco G, Busch E, Patel S, Singewald N, Holmes A. Prefrontal inputs to the amygdala instruct fear extinction memory formation. Sci Adv. 2015 Jul;1(6). doi: 10.1126/sciadv.1500251. Epub 2015 Jul 31. PMID: 26504902; PMCID: PMC4618669.
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One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions.

Inorganic chemistry

Bosch E, Barnes CL.
PMID: 11978124
Inorg Chem. 2002 May 06;41(9):2543-7. doi: 10.1021/ic010795q.

The self-assembly of coordination networks from reaction of 2,4,6-trimesityl-1,3,5-triazine and silver(I) trifluoroacetate is described. A one-dimensional linear polymer is formed from solutions deficient in silver while a two-dimensional, graphite-like sheet is formed from solutions containing 3 equiv of silver...

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Bosch E, Barnes CL. One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorg Chem. 2002;41(9):2543-7doi: 10.1021/ic010795q.
Bosch, E., & Barnes, C. L. (2002). One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorganic chemistry, 41(9), 2543-7. https://doi.org/10.1021/ic010795q
Bosch, Eric, and Barnes, Charles L. "One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions." Inorganic chemistry vol. 41,9 (2002): 2543-7. doi: https://doi.org/10.1021/ic010795q
Bosch E, Barnes CL. One- and two-dimensional silver-coordination networks containing pi-sandwiched silver-silver interactions. Inorg Chem. 2002 May 06;41(9):2543-7. doi: 10.1021/ic010795q. PMID: 11978124.
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1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride.

Inorganic chemistry

Bosch E, Barnes CL.
PMID: 11399178
Inorg Chem. 2001 Jun 18;40(13):3097-100. doi: 10.1021/ic010058u.

The design, synthesis, and complexation characteristics of the bipyridyl ligand 1,2-bis-(2-pyridylethynyl)benzene are described. The X-ray crystallographic characterization of the 1:1 complexes of 1,2-bis(2-pyridylethynyl)benzene with silver(I) triflate and palladium(II) chloride are described. In the X-ray crystal structure of the silver(I)...

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Bosch E, Barnes CL. 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorg Chem. 2001;40(13):3097-100doi: 10.1021/ic010058u.
Bosch, E., & Barnes, C. L. (2001). 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorganic chemistry, 40(13), 3097-100. https://doi.org/10.1021/ic010058u
Bosch, E, and Barnes, C L. "1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride." Inorganic chemistry vol. 40,13 (2001): 3097-100. doi: https://doi.org/10.1021/ic010058u
Bosch E, Barnes CL. 1,2-Bis(2-pyridylethynyl)benzene, a novel trans-chelating bipyridyl ligand. structural characterization of the complexes with silver(I) triflate and palladium(II) chloride. Inorg Chem. 2001 Jun 18;40(13):3097-100. doi: 10.1021/ic010058u. PMID: 11399178.
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A QSPR study of the p solute polarity parameter to estimate retention in HPLC.

Journal of chemical information and computer sciences

Bosque R, Sales J, Bosch E, Rosés M, García-Alvarez-Coque MC, Torres-Lapasió JR.
PMID: 12870917
J Chem Inf Comput Sci. 2003 Jul-Aug;43(4):1240-7. doi: 10.1021/ci0340660.

A Quantitative Structure-Property Relationship (QSPR) model is developed to calculate the solute polarity parameter p of a set of 233 compounds of a very different chemical nature. The proposed model, derived from multiple linear regression, contains four descriptors calculated...

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Bosque R, Sales J, Bosch E, et al. A QSPR study of the p solute polarity parameter to estimate retention in HPLC. J Chem Inf Comput Sci. 2003;43(4):1240-7doi: 10.1021/ci0340660.
Bosque, R., Sales, J., Bosch, E., Rosés, M., García-Alvarez-Coque, M. C., & Torres-Lapasió, J. R. (2003). A QSPR study of the p solute polarity parameter to estimate retention in HPLC. Journal of chemical information and computer sciences, 43(4), 1240-7. https://doi.org/10.1021/ci0340660
Bosque, Ramón, et al. "A QSPR study of the p solute polarity parameter to estimate retention in HPLC." Journal of chemical information and computer sciences vol. 43,4 (2003): 1240-7. doi: https://doi.org/10.1021/ci0340660
Bosque R, Sales J, Bosch E, Rosés M, García-Alvarez-Coque MC, Torres-Lapasió JR. A QSPR study of the p solute polarity parameter to estimate retention in HPLC. J Chem Inf Comput Sci. 2003 Jul-Aug;43(4):1240-7. doi: 10.1021/ci0340660. PMID: 12870917.
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A comparative study of some hydroxyanthraquinones as acid-base indicators.

Talanta

Barbosa J, Bosch E, Carrera R.
PMID: 18963955
Talanta. 1985 Nov;32(11):1077-81. doi: 10.1016/0039-9140(85)80129-6.

Alizarin, Alizarin S, quinizarin and quinalizarin have been compared as acid-base indicators with Bromocresol Green and Methyl Orange as reference indicators. The chromaticity co-ordinates, complementary chromaticity co-ordinates, pK(a) values, transition pH-range, pH of maximum colour change, optimum concentration for...

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Barbosa J, Bosch E, Carrera R. A comparative study of some hydroxyanthraquinones as acid-base indicators. Talanta. 1985;32(11):1077-81doi: 10.1016/0039-9140(85)80129-6.
Barbosa, J., Bosch, E., & Carrera, R. (1985). A comparative study of some hydroxyanthraquinones as acid-base indicators. Talanta, 32(11), 1077-81. https://doi.org/10.1016/0039-9140(85)80129-6
Barbosa, J, et al. "A comparative study of some hydroxyanthraquinones as acid-base indicators." Talanta vol. 32,11 (1985): 1077-81. doi: https://doi.org/10.1016/0039-9140(85)80129-6
Barbosa J, Bosch E, Carrera R. A comparative study of some hydroxyanthraquinones as acid-base indicators. Talanta. 1985 Nov;32(11):1077-81. doi: 10.1016/0039-9140(85)80129-6. PMID: 18963955.
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Wild yam (Dioscoreaceae).

Journal of herbal pharmacotherapy

Ulbricht C, Basch E, Ulbricht C, Sollars D, Hammerness P, Hashmi S.
PMID: 15277124
J Herb Pharmacother. 2003;3(4):77-91.

No abstract available.

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Ulbricht C, Basch E, Ulbricht C, et al. Wild yam (Dioscoreaceae). J Herb Pharmacother. 2003;3(4):77-91
Ulbricht, C., Basch, E., Ulbricht, C., Sollars, D., Hammerness, P., & Hashmi, S. (2003). Wild yam (Dioscoreaceae). Journal of herbal pharmacotherapy, 3(4), 77-91.
Ulbricht, Catherine, et al. "Wild yam (Dioscoreaceae)." Journal of herbal pharmacotherapy vol. 3,4 (2003): 77-91.
Ulbricht C, Basch E, Ulbricht C, Sollars D, Hammerness P, Hashmi S. Wild yam (Dioscoreaceae). J Herb Pharmacother. 2003;3(4):77-91. PMID: 15277124.
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Study of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium Evaluation of colour-change limits through complementary chromaticity parameters.

Talanta

Barbosa J, Sanchez J, Bosch E.
PMID: 18963587
Talanta. 1984 Apr;31(4):279-82. doi: 10.1016/0039-9140(84)80277-5.

The use of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium is proposed. The acid dissociation constants of the indicator in isopropyl alcohol solution are pK(a1) = 12.95 +/- 0.03 and pK(a2) = 15.96 +/- 0.07. The sharpness...

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Barbosa J, Sanchez J, Bosch E. Study of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium Evaluation of colour-change limits through complementary chromaticity parameters. Talanta. 1984;31(4):279-82doi: 10.1016/0039-9140(84)80277-5.
Barbosa, J., Sanchez, J., & Bosch, E. (1984). Study of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium Evaluation of colour-change limits through complementary chromaticity parameters. Talanta, 31(4), 279-82. https://doi.org/10.1016/0039-9140(84)80277-5
Barbosa, J, et al. "Study of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium Evaluation of colour-change limits through complementary chromaticity parameters." Talanta vol. 31,4 (1984): 279-82. doi: https://doi.org/10.1016/0039-9140(84)80277-5
Barbosa J, Sanchez J, Bosch E. Study of 1,4-dihydroxyanthraquinone as an acid-base indicator in isopropyl alcohol medium Evaluation of colour-change limits through complementary chromaticity parameters. Talanta. 1984 Apr;31(4):279-82. doi: 10.1016/0039-9140(84)80277-5. PMID: 18963587.
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Ionic equilibria in neutral amphiprotic solvents of low dielectric constant: Buffer solutions.

Talanta

Bosch E, Rosés M.
PMID: 18964768
Talanta. 1989 Jun;36(6):615-21. doi: 10.1016/0039-9140(89)80251-6.

The ionic equilibria in neutral amphiprotic solvents (isopropyl and tert-butyl alcohols) have been established, and equations to calculate pH values in solutions of acids, bases, salts or their mixtures, developed. The effect, on the dissociation equilibria, of the presence...

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Bosch E, Rosés M. Ionic equilibria in neutral amphiprotic solvents of low dielectric constant: Buffer solutions. Talanta. 1989;36(6):615-21doi: 10.1016/0039-9140(89)80251-6.
Bosch, E., & Rosés, M. (1989). Ionic equilibria in neutral amphiprotic solvents of low dielectric constant: Buffer solutions. Talanta, 36(6), 615-21. https://doi.org/10.1016/0039-9140(89)80251-6
Bosch, E, and Rosés, M. "Ionic equilibria in neutral amphiprotic solvents of low dielectric constant: Buffer solutions." Talanta vol. 36,6 (1989): 615-21. doi: https://doi.org/10.1016/0039-9140(89)80251-6
Bosch E, Rosés M. Ionic equilibria in neutral amphiprotic solvents of low dielectric constant: Buffer solutions. Talanta. 1989 Jun;36(6):615-21. doi: 10.1016/0039-9140(89)80251-6. PMID: 18964768.
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Showing 1 to 12 of 238 entries