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Effective leadership: A toolkit for the 21st-century historically Black college and university president

Minority serving Institution STEM training

Commodore F, Esters LT, Gasman M.
GSID: P8Fe16y5HF0J
LT Esters, A Washington, M Gasman, F Commodore… - … Minority Serving Institutions, 2016

No abstract available.

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Esters, L. T., Washington, A., Gasman, M., Commodore, F., O’Neal, B., Freeman, S., & Jimenez, D. (2016). Effective leadership: A toolkit for the 21st-century historically Black college and university president. Penn Center for Minority Serving Institutions.
Esters, Levon T., et al. "Effective leadership: A toolkit for the 21st-century historically Black college and university president." Penn Center for Minority Serving Institutions (2016).
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Enhancing STEM Education at Minority and Underrepresented Institutions through the Center for Applied Atmospheric Research and Education (CAARE)

STEM and underrepresented

Estes MG, Griffin R.
GSID: HcqSO8nmLg0J
MG Estes Jr, R Griffin, MZ Al-Hamdan… - AGU Fall Meeting …, 2016 - ui.adsabs.harvard.edu

Abstract Funding from The NASA MUREP Institutional Research Opportunity (MIRO) Program established the Center for Applied Atmospheric Research and Education (CAARE) to promote STEM literacy and enhance the capability to support NASA's Earth Science Mission Directorate. Through CAARE opportunities...

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Estes Jr, M. G., Griffin, R., Al-Hamdan, M. Z., Estes, S. M., Crosson, W. L., & Chiao, S. (2016, December). Enhancing STEM Education at Minority and Underrepresented Institutions through the Center for Applied Atmospheric Research and Education (CAARE). In AGU Fall Meeting Abstracts (Vol. 2016, pp. ED43B-0861).
Estes Jr, M. G., et al. "Enhancing STEM Education at Minority and Underrepresented Institutions through the Center for Applied Atmospheric Research and Education (CAARE)." AGU Fall Meeting Abstracts. Vol. 2016. 2016.
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An Evaluation of a Mentoring Training Program Focused on Women and Underrepresented Minorities in Ag+ STEM Programs: A Case Study

STEM and underrepresented

Esters LT, Knobloch NA.
GSID: Z1h8kTcbfAcJ
BCM Allen, NA Knobloch, LT Esters - NACTA Journal, 2019 - search.ebscohost.com

… towards success within agriculture and other STEM disciplines. The findings from this … +STEM disciplines. If we are to effectively promote diversity within the Ag+STEM disciplines, …

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Allen, B. C. M., Knobloch, N. A., & Esters, L. T. (2019). An Evaluation of a Mentoring Training Program Focused on Women and Underrepresented Minorities in Ag+ STEM Programs: A Case Study. NACTA Journal, 63(1).
Allen, B. C. M., N. A. Knobloch, and L. T. Esters. "An Evaluation of a Mentoring Training Program Focused on Women and Underrepresented Minorities in Ag+ STEM Programs: A Case Study." NACTA Journal 63.1 (2019).
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Trophic upgrading and mobilization of wax esters in microzooplankton

EPSCoR Research Infrastructure Improvement Program AND Program Evaluation

D'Souza N.
GSID: kna0IKWjZKwJ
K Roohani, BA Haubrich, KL Yue, N D'Souza… - PeerJ, 2019 - peerj.com

Heterotrophic protists play pivotal roles in aquatic ecosystems by transferring matter and energy, including lipids, from primary producers to higher trophic predators. Using Oxyrrhis marina as a model organism, changes to the non-saponifiable protist lipids were investigated under satiation...

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Roohani, K., Haubrich, B. A., Yue, K. L., D’Souza, N., Montalbano, A., Rynearson, T., ... & Reid, C. W. (2019). Trophic upgrading and mobilization of wax esters in microzooplankton. PeerJ, 7, e7549.
Roohani, Keyana, et al. "Trophic upgrading and mobilization of wax esters in microzooplankton." PeerJ 7 (2019): e7549.
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[General and sedative action of some esters of 4-piperidino-cyclohexanol].

Bollettino chimico farmaceutico

Ottaviano G.
PMID: 5999994
Boll Chim Farm. 1966 Oct;105(10):719-25.

No abstract available.

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Ottaviano G. Azione generale e sedativa di alcuni esteri del 4-piperidino-cicloesanolo. [General and sedative action of some esters of 4-piperidino-cyclohexanol]. Boll Chim Farm. 1966;105(10):719-25
Ottaviano, G. (1966). Azione generale e sedativa di alcuni esteri del 4-piperidino-cicloesanolo. [General and sedative action of some esters of 4-piperidino-cyclohexanol]. Bollettino chimico farmaceutico, 105(10), 719-25.
Ottaviano, G. "Azione generale e sedativa di alcuni esteri del 4-piperidino-cicloesanolo." [General and sedative action of some esters of 4-piperidino-cyclohexanol]. Bollettino chimico farmaceutico vol. 105,10 (1966): 719-25.
Ottaviano G. Azione generale e sedativa di alcuni esteri del 4-piperidino-cicloesanolo. [General and sedative action of some esters of 4-piperidino-cyclohexanol]. Boll Chim Farm. 1966 Oct;105(10):719-25. Italian. PMID: 5999994.
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First pre-functionalised polymeric aromatic framework from mononitrotetrakis(iodophenyl)methane and its applications.

Chemistry (Weinheim an der Bergstrasse, Germany)

Verde-Sesto E, Pintado-Sierra M, Corma A, Maya EM, de la Campa JG, Iglesias M, Sánchez F.
PMID: 24623578
Chemistry. 2014 Apr 22;20(17):5111-20. doi: 10.1002/chem.201304163. Epub 2014 Mar 12.

Starting from mononitrotetrakis(iodophenyl)methane as monomer, we report the preparation of the first pre-functionalised porous aromatic frameworks (PAFs) and their application as supports for organometallic catalysts. Neutral coordinate imino-pyridine Schiff base (PAF-NPy) or chiral bis-amino (PAF-NPro) ligands were obtained by...

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Verde-Sesto E, Pintado-Sierra M, Corma A, et al. First pre-functionalised polymeric aromatic framework from mononitrotetrakis(iodophenyl)methane and its applications. Chemistry. 2014;20(17):5111-20doi: 10.1002/chem.201304163.
Verde-Sesto, E., Pintado-Sierra, M., Corma, A., Maya, E. M., de la Campa, J. G., Iglesias, M., & Sánchez, F. (2014). First pre-functionalised polymeric aromatic framework from mononitrotetrakis(iodophenyl)methane and its applications. Chemistry (Weinheim an der Bergstrasse, Germany), 20(17), 5111-20. https://doi.org/10.1002/chem.201304163
Verde-Sesto, Ester, et al. "First pre-functionalised polymeric aromatic framework from mononitrotetrakis(iodophenyl)methane and its applications." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 20,17 (2014): 5111-20. doi: https://doi.org/10.1002/chem.201304163
Verde-Sesto E, Pintado-Sierra M, Corma A, Maya EM, de la Campa JG, Iglesias M, Sánchez F. First pre-functionalised polymeric aromatic framework from mononitrotetrakis(iodophenyl)methane and its applications. Chemistry. 2014 Apr 22;20(17):5111-20. doi: 10.1002/chem.201304163. Epub 2014 Mar 12. PMID: 24623578.
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Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide.

Chemistry (Weinheim an der Bergstrasse, Germany)

Chen CY, Chen CT.
PMID: 24123627
Chemistry. 2013 Nov 18;19(47):16050-7. doi: 10.1002/chem.201302342. Epub 2013 Oct 10.

A novel reaction-based cross-linked polymeric nanoprobe with a self-calibrating ratiometric fluorescence readout to selectively detect H2O2 is reported. The polymeric nanoprobe is fabricated by using hydrophobic H2O2-reactive boronic ester groups, crosslinker units, and environmentally sensitive 3-hydroxyflavone fluorophores through a...

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Chen CY, Chen CT. Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry. 2013;19(47):16050-7doi: 10.1002/chem.201302342.
Chen, C. Y., & Chen, C. T. (2013). Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry (Weinheim an der Bergstrasse, Germany), 19(47), 16050-7. https://doi.org/10.1002/chem.201302342
Chen, Chun-Yen, and Chen, Chao-Tsen. "Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 19,47 (2013): 16050-7. doi: https://doi.org/10.1002/chem.201302342
Chen CY, Chen CT. Reaction-based and single fluorescent emitter decorated ratiometric nanoprobe to detect hydrogen peroxide. Chemistry. 2013 Nov 18;19(47):16050-7. doi: 10.1002/chem.201302342. Epub 2013 Oct 10. PMID: 24123627.
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Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters.

Journal of the American Society for Mass Spectrometry

Isbell JJ, Brodbelt JS.
PMID: 24203429
J Am Soc Mass Spectrom. 1996 Jun;7(6):565-72. doi: 10.1016/1044-0305(96)00016-5.

Functional group interactions have been observed to affect gas-phase ion-molecule chemistry in a quadrupole ion trap mass spectrometer. Gas-phase methylation and collisionactivated dissociation reactions of a series of related acids and esters allows an evaluation of the structural factors...

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Isbell JJ, Brodbelt JS. Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters. J Am Soc Mass Spectrom. 1996;7(6):565-72doi: 10.1016/1044-0305(96)00016-5.
Isbell, J. J., & Brodbelt, J. S. (1996). Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters. Journal of the American Society for Mass Spectrometry, 7(6), 565-72. https://doi.org/10.1016/1044-0305(96)00016-5
Isbell, J J, and Brodbelt, J S. "Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters." Journal of the American Society for Mass Spectrometry vol. 7,6 (1996): 565-72. doi: https://doi.org/10.1016/1044-0305(96)00016-5
Isbell JJ, Brodbelt JS. Effects of functional group interactions on the gas-phase methylation and dissociation of acids and esters. J Am Soc Mass Spectrom. 1996 Jun;7(6):565-72. doi: 10.1016/1044-0305(96)00016-5. PMID: 24203429.
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Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2.

Journal of the American Chemical Society

Moragas T, Cornella J, Martin R.
PMID: 25473825
J Am Chem Soc. 2014 Dec 24;136(51):17702-5. doi: 10.1021/ja509077a. Epub 2014 Dec 12.

A novel Ni-catalyzed regiodivergent reductive carboxylation of allyl esters with CO2 has been developed. This mild, user-friendly, and operationally simple method is characterized by an exquisite selectivity profile that is dictated by the ligand backbone.

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Moragas T, Cornella J, Martin R. Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2. J Am Chem Soc. 2014;136(51):17702-5doi: 10.1021/ja509077a.
Moragas, T., Cornella, J., & Martin, R. (2014). Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2. Journal of the American Chemical Society, 136(51), 17702-5. https://doi.org/10.1021/ja509077a
Moragas, Toni, et al. "Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2." Journal of the American Chemical Society vol. 136,51 (2014): 17702-5. doi: https://doi.org/10.1021/ja509077a
Moragas T, Cornella J, Martin R. Ligand-controlled regiodivergent Ni-catalyzed reductive carboxylation of allyl esters with CO2. J Am Chem Soc. 2014 Dec 24;136(51):17702-5. doi: 10.1021/ja509077a. Epub 2014 Dec 12. PMID: 25473825.
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Immunohistochemical Study of Aquaporins in an African Grey Parrot (Psittacus erithacus) With Hydrocephalus.

Journal of avian medicine and surgery

Blasco E, Martorell J, De la Fuente C, Pumarola M.
PMID: 25843469
J Avian Med Surg. 2014 Dec;28(4):309-15. doi: 10.1647/2013-059.

A 5-month-old African grey parrot (Psittacus erithacus) was examined after 3 weeks of weakness, ataxia, mental depression, and seizures. Results of a complete blood cell count and plasma biochemical analysis were unremarkable. Magnetic resonance imaging revealed a severe bilateral...

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Blasco E, Martorell J, De la Fuente C, et al. Immunohistochemical Study of Aquaporins in an African Grey Parrot (Psittacus erithacus) With Hydrocephalus. J Avian Med Surg. 2014;28(4):309-15doi: 10.1647/2013-059.
Blasco, E., Martorell, J., De la Fuente, C., & Pumarola, M. (2014). Immunohistochemical Study of Aquaporins in an African Grey Parrot (Psittacus erithacus) With Hydrocephalus. Journal of avian medicine and surgery, 28(4), 309-15. https://doi.org/10.1647/2013-059
Blasco, Ester, et al. "Immunohistochemical Study of Aquaporins in an African Grey Parrot (Psittacus erithacus) With Hydrocephalus." Journal of avian medicine and surgery vol. 28,4 (2014): 309-15. doi: https://doi.org/10.1647/2013-059
Blasco E, Martorell J, De la Fuente C, Pumarola M. Immunohistochemical Study of Aquaporins in an African Grey Parrot (Psittacus erithacus) With Hydrocephalus. J Avian Med Surg. 2014 Dec;28(4):309-15. doi: 10.1647/2013-059. PMID: 25843469.
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Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3.

The Journal of organic chemistry

Venkatesham K, Bhujanga Rao C, Dokuburra CB, Bunce RA, Venkateswarlu Y.
PMID: 26497695
J Org Chem. 2015 Nov 20;80(22):11611-7. doi: 10.1021/acs.joc.5b02143. Epub 2015 Oct 30.

A new and efficient method has been developed for the synthesis of thioethers from carboxylates and thiols. The reaction proceeds via a Fe(III)-catalyzed direct displacement of carboxylates from benzylic or allylic esters by heterocyclic thiols. Short reaction times, good...

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Venkatesham K, Bhujanga Rao C, Dokuburra CB, et al. Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3. J Org Chem. 2015;80(22):11611-7doi: 10.1021/acs.joc.5b02143.
Venkatesham, K., Bhujanga Rao, C., Dokuburra, C. B., Bunce, R. A., & Venkateswarlu, Y. (2015). Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3. The Journal of organic chemistry, 80(22), 11611-7. https://doi.org/10.1021/acs.joc.5b02143
Venkatesham, Kunuru, et al. "Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3." The Journal of organic chemistry vol. 80,22 (2015): 11611-7. doi: https://doi.org/10.1021/acs.joc.5b02143
Venkatesham K, Bhujanga Rao C, Dokuburra CB, Bunce RA, Venkateswarlu Y. Direct Synthesis of Thioethers from Carboxylates and Thiols Catalyzed by FeCl3. J Org Chem. 2015 Nov 20;80(22):11611-7. doi: 10.1021/acs.joc.5b02143. Epub 2015 Oct 30. PMID: 26497695.
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Cholanamide components for organic alloys; expanding the scope of nanoporous steroidal ureas.

Chemical communications (Cambridge, England)

Travaglini L, Bridgland LN, Davis AP.
PMID: 24686843
Chem Commun (Camb). 2014 May 14;50(37):4803-5. doi: 10.1039/c4cc01256a.

Amide-linked side-chains can substitute for esters in crystalline nanoporous steroidal ureas (NSPUs). This efficient conjugation method increases the versatility of NPSUs, and should aid the inclusion of complex functional units in the crystal channels.

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Travaglini L, Bridgland LN, Davis AP. Cholanamide components for organic alloys; expanding the scope of nanoporous steroidal ureas. Chem Commun (Camb). 2014;50(37):4803-5doi: 10.1039/c4cc01256a.
Travaglini, L., Bridgland, L. N., & Davis, A. P. (2014). Cholanamide components for organic alloys; expanding the scope of nanoporous steroidal ureas. Chemical communications (Cambridge, England), 50(37), 4803-5. https://doi.org/10.1039/c4cc01256a
Travaglini, Leana, et al. "Cholanamide components for organic alloys; expanding the scope of nanoporous steroidal ureas." Chemical communications (Cambridge, England) vol. 50,37 (2014): 4803-5. doi: https://doi.org/10.1039/c4cc01256a
Travaglini L, Bridgland LN, Davis AP. Cholanamide components for organic alloys; expanding the scope of nanoporous steroidal ureas. Chem Commun (Camb). 2014 May 14;50(37):4803-5. doi: 10.1039/c4cc01256a. PMID: 24686843.
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Showing 13 to 24 of 11189 entries