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Optical pseudomotors for soft x-ray beamlines.

The Review of scientific instruments

Pedreira P, Sics I, Sorrentino A, Pereiro E, Aballe L, Foerster M, Pérez-Dieste V, Escudero C, Nicolas J.
PMID: 27250382
Rev Sci Instrum. 2016 May;87(5):052002. doi: 10.1063/1.4949339.

Optical elements of soft x-ray beamlines usually have motorized translations and rotations that allow for the fine alignment of the beamline. This is to steer the photon beam at some positions and to correct the focus on slits or...

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Pedreira P, Sics I, Sorrentino A, et al. Optical pseudomotors for soft x-ray beamlines. Rev Sci Instrum. 2016;87(5):052002doi: 10.1063/1.4949339.
Pedreira, P., Sics, I., Sorrentino, A., Pereiro, E., Aballe, L., Foerster, M., Pérez-Dieste, V., Escudero, C., & Nicolas, J. (2016). Optical pseudomotors for soft x-ray beamlines. The Review of scientific instruments, 87(5), 052002. https://doi.org/10.1063/1.4949339
Pedreira, P, et al. "Optical pseudomotors for soft x-ray beamlines." The Review of scientific instruments vol. 87,5 (2016): 052002. doi: https://doi.org/10.1063/1.4949339
Pedreira P, Sics I, Sorrentino A, Pereiro E, Aballe L, Foerster M, Pérez-Dieste V, Escudero C, Nicolas J. Optical pseudomotors for soft x-ray beamlines. Rev Sci Instrum. 2016 May;87(5):052002. doi: 10.1063/1.4949339. PMID: 27250382.
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Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes.

Journal of the American Chemical Society

Schäfer M, Beattie NA, Geetharani K, Schäfer J, Ewing WC, Krahfuß M, Hörl C, Dewhurst RD, Macgregor SA, Lambert C, Braunschweig H.
PMID: 27286231
J Am Chem Soc. 2016 Jul 06;138(26):8212-20. doi: 10.1021/jacs.6b04128. Epub 2016 Jun 27.

Di-tert-butyliminoborane is found to be a very useful synthon for the synthesis of a variety of functionalized 1,4-azaborinines by the Rh-mediated cyclization of iminoboranes with alkynes. The reactions proceed via [2 + 2] cycloaddition of iminoboranes and alkynes in...

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Schäfer M, Beattie NA, Geetharani K, et al. Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. J Am Chem Soc. 2016;138(26):8212-20doi: 10.1021/jacs.6b04128.
Schäfer, M., Beattie, N. A., Geetharani, K., Schäfer, J., Ewing, W. C., Krahfuß, M., Hörl, C., Dewhurst, R. D., Macgregor, S. A., Lambert, C., & Braunschweig, H. (2016). Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. Journal of the American Chemical Society, 138(26), 8212-20. https://doi.org/10.1021/jacs.6b04128
Schäfer, Marius, et al. "Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes." Journal of the American Chemical Society vol. 138,26 (2016): 8212-20. doi: https://doi.org/10.1021/jacs.6b04128
Schäfer M, Beattie NA, Geetharani K, Schäfer J, Ewing WC, Krahfuß M, Hörl C, Dewhurst RD, Macgregor SA, Lambert C, Braunschweig H. Synthesis of Functionalized 1,4-Azaborinines by the Cyclization of Di-tert-butyliminoborane and Alkynes. J Am Chem Soc. 2016 Jul 06;138(26):8212-20. doi: 10.1021/jacs.6b04128. Epub 2016 Jun 27. PMID: 27286231.
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Tunable Approach for the Stereoselective Synthesis of 1-C-Diethylphosphono(difluoromethyl) Iminosugars as Glycosyl Phosphate Mimics.

The Journal of organic chemistry

Cocaud C, Nicolas C, Poisson T, Pannecoucke X, Legault CY, Martin OR.
PMID: 28221798
J Org Chem. 2017 Mar 03;82(5):2753-2763. doi: 10.1021/acs.joc.6b03071. Epub 2017 Feb 21.

An efficient methodology for the stereoselective and tunable addition of LiCF

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Cocaud C, Nicolas C, Poisson T, et al. Tunable Approach for the Stereoselective Synthesis of 1-C-Diethylphosphono(difluoromethyl) Iminosugars as Glycosyl Phosphate Mimics. J Org Chem. 2017;82(5):2753-2763doi: 10.1021/acs.joc.6b03071.
Cocaud, C., Nicolas, C., Poisson, T., Pannecoucke, X., Legault, C. Y., & Martin, O. R. (2017). Tunable Approach for the Stereoselective Synthesis of 1-C-Diethylphosphono(difluoromethyl) Iminosugars as Glycosyl Phosphate Mimics. The Journal of organic chemistry, 82(5), 2753-2763. https://doi.org/10.1021/acs.joc.6b03071
Cocaud, Chloé, et al. "Tunable Approach for the Stereoselective Synthesis of 1-C-Diethylphosphono(difluoromethyl) Iminosugars as Glycosyl Phosphate Mimics." The Journal of organic chemistry vol. 82,5 (2017): 2753-2763. doi: https://doi.org/10.1021/acs.joc.6b03071
Cocaud C, Nicolas C, Poisson T, Pannecoucke X, Legault CY, Martin OR. Tunable Approach for the Stereoselective Synthesis of 1-C-Diethylphosphono(difluoromethyl) Iminosugars as Glycosyl Phosphate Mimics. J Org Chem. 2017 Mar 03;82(5):2753-2763. doi: 10.1021/acs.joc.6b03071. Epub 2017 Feb 21. PMID: 28221798.
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Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents.

Chemistry (Weinheim an der Bergstrasse, Germany)

Hanson SS, Richard NA, Dyker CA.
PMID: 25877958
Chemistry. 2015 May 26;21(22):8052-5. doi: 10.1002/chem.201500809. Epub 2015 Apr 15.

Four members of a new family of powerful bispyridinylidene organic reducing agents have been prepared, which exploit iminophosphorano (-N=PR3; R = Ph, Cy) π-donor substituents. Electrochemical studies show exceptionally high oxidation potentials, ranging from 1.30 to 1.51 V versus...

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Hanson SS, Richard NA, Dyker CA. Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents. Chemistry. 2015;21(22):8052-5doi: 10.1002/chem.201500809.
Hanson, S. S., Richard, N. A., & Dyker, C. A. (2015). Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents. Chemistry (Weinheim an der Bergstrasse, Germany), 21(22), 8052-5. https://doi.org/10.1002/chem.201500809
Hanson, Samuel S, et al. "Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents." Chemistry (Weinheim an der Bergstrasse, Germany) vol. 21,22 (2015): 8052-5. doi: https://doi.org/10.1002/chem.201500809
Hanson SS, Richard NA, Dyker CA. Powerful Bispyridinylidene Organic Reducing Agents with Iminophosphorano π-Donor Substituents. Chemistry. 2015 May 26;21(22):8052-5. doi: 10.1002/chem.201500809. Epub 2015 Apr 15. PMID: 25877958.
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Social Environment Shapes the Speed of Cooperation.

Scientific reports

Nishi A, Christakis NA, Evans AM, O'Malley AJ, Rand DG.
PMID: 27435940
Sci Rep. 2016 Jul 20;6:29622. doi: 10.1038/srep29622.

Are cooperative decisions typically made more quickly or slowly than non-cooperative decisions? While this question has attracted considerable attention in recent years, most research has focused on one-shot interactions. Yet it is repeated interactions that characterize most important real-world...

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Nishi A, Christakis NA, Evans AM, et al. Social Environment Shapes the Speed of Cooperation. Sci Rep. 2016;6:29622doi: 10.1038/srep29622.
Nishi, A., Christakis, N. A., Evans, A. M., O'Malley, A. J., & Rand, D. G. (2016). Social Environment Shapes the Speed of Cooperation. Scientific reports, 629622. https://doi.org/10.1038/srep29622
Nishi, Akihiro, et al. "Social Environment Shapes the Speed of Cooperation." Scientific reports vol. 6 (2016): 29622. doi: https://doi.org/10.1038/srep29622
Nishi A, Christakis NA, Evans AM, O'Malley AJ, Rand DG. Social Environment Shapes the Speed of Cooperation. Sci Rep. 2016 Jul 20;6:29622. doi: 10.1038/srep29622. PMID: 27435940; PMCID: PMC4951649.
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A particular effect of sleep, but not pain or depression, on the blood-oxygen-level dependent response during working memory tasks in patients with chronic pain.

Journal of pain research

Elvemo NA, Landrø NI, Borchgrevink PC, Håberg AK.
PMID: 26185465
J Pain Res. 2015 Jul 07;8:335-46. doi: 10.2147/JPR.S83486. eCollection 2015.

BACKGROUND: Patients with chronic pain (CP) are often reported to have deficits in working memory. Pain impairs working memory, but so do depression and sleep problems, which are also common in CP. Depression has been linked to changes in...

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Elvemo NA, Landrø NI, Borchgrevink PC, et al. A particular effect of sleep, but not pain or depression, on the blood-oxygen-level dependent response during working memory tasks in patients with chronic pain. J Pain Res. 2015;8:335-46doi: 10.2147/JPR.S83486.
Elvemo, N. A., Landrø, N. I., Borchgrevink, P. C., & Håberg, A. K. (2015). A particular effect of sleep, but not pain or depression, on the blood-oxygen-level dependent response during working memory tasks in patients with chronic pain. Journal of pain research, 8335-46. https://doi.org/10.2147/JPR.S83486
Elvemo, Nicolas A, et al. "A particular effect of sleep, but not pain or depression, on the blood-oxygen-level dependent response during working memory tasks in patients with chronic pain." Journal of pain research vol. 8 (2015): 335-46. doi: https://doi.org/10.2147/JPR.S83486
Elvemo NA, Landrø NI, Borchgrevink PC, Håberg AK. A particular effect of sleep, but not pain or depression, on the blood-oxygen-level dependent response during working memory tasks in patients with chronic pain. J Pain Res. 2015 Jul 07;8:335-46. doi: 10.2147/JPR.S83486. eCollection 2015. PMID: 26185465; PMCID: PMC4500611.
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Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity.

ACS medicinal chemistry letters

Regueiro-Ren A, Liu Z, Chen Y, Sin N, Sit SY, Swidorski JJ, Chen J, Venables BL, Zhu J, Nowicka-Sans B, Protack T, Lin Z, Terry B, Samanta H, Zhang S, Li Z, Beno BR, Huang XS, Rahematpura S, Parker DD, Haskell R, Jenkins S, Santone KS, Cockett MI, Krystal M, Meanwell NA, Hanumegowda U, Dicker IB.
PMID: 27326328
ACS Med Chem Lett. 2016 Apr 22;7(6):568-72. doi: 10.1021/acsmedchemlett.6b00010. eCollection 2016 Jun 09.

HIV-1 maturation inhibition (MI) has been clinically validated as an approach to the control of HIV-1 infection. However, identifying an MI with both broad polymorphic spectrum coverage and good oral exposure has been challenging. Herein, we describe the design,...

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Regueiro-Ren A, Liu Z, Chen Y, et al. Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity. ACS Med Chem Lett. 2016;7(6):568-72doi: 10.1021/acsmedchemlett.6b00010.
Regueiro-Ren, A., Liu, Z., Chen, Y., Sin, N., Sit, S. Y., Swidorski, J. J., Chen, J., Venables, B. L., Zhu, J., Nowicka-Sans, B., Protack, T., Lin, Z., Terry, B., Samanta, H., Zhang, S., Li, Z., Beno, B. R., Huang, X. S., Rahematpura, S., Parker, D. D., Haskell, R., Jenkins, S., Santone, K. S., Cockett, M. I., Krystal, M., Meanwell, N. A., Hanumegowda, U., & Dicker, I. B. (2016). Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity. ACS medicinal chemistry letters, 7(6), 568-72. https://doi.org/10.1021/acsmedchemlett.6b00010
Regueiro-Ren, Alicia, et al. "Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity." ACS medicinal chemistry letters vol. 7,6 (2016): 568-72. doi: https://doi.org/10.1021/acsmedchemlett.6b00010
Regueiro-Ren A, Liu Z, Chen Y, Sin N, Sit SY, Swidorski JJ, Chen J, Venables BL, Zhu J, Nowicka-Sans B, Protack T, Lin Z, Terry B, Samanta H, Zhang S, Li Z, Beno BR, Huang XS, Rahematpura S, Parker DD, Haskell R, Jenkins S, Santone KS, Cockett MI, Krystal M, Meanwell NA, Hanumegowda U, Dicker IB. Discovery of BMS-955176, a Second Generation HIV-1 Maturation Inhibitor with Broad Spectrum Antiviral Activity. ACS Med Chem Lett. 2016 Apr 22;7(6):568-72. doi: 10.1021/acsmedchemlett.6b00010. eCollection 2016 Jun 09. PMID: 27326328; PMCID: PMC4904268.
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A .

Acta crystallographica. Section C, Structural chemistry

Vigilante NJ, Mehta MA.
PMID: 28257018
Acta Crystallogr C Struct Chem. 2017 Mar 01;73:234-243. doi: 10.1107/S2053229617000869. Epub 2017 Feb 06.

We report an analysis of the

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Vigilante NJ, Mehta MA. A . Acta Crystallogr C Struct Chem. 2017;73:234-243doi: 10.1107/S2053229617000869.
Vigilante, N. J., & Mehta, M. A. (2017). A . Acta crystallographica. Section C, Structural chemistry, 73234-243. https://doi.org/10.1107/S2053229617000869
Vigilante, Nicolas J, and Mehta, Manish A. "A ." Acta crystallographica. Section C, Structural chemistry vol. 73 (2017): 234-243. doi: https://doi.org/10.1107/S2053229617000869
Vigilante NJ, Mehta MA. A . Acta Crystallogr C Struct Chem. 2017 Mar 01;73:234-243. doi: 10.1107/S2053229617000869. Epub 2017 Feb 06. PMID: 28257018.
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Association of hospital and physician case volumes with cardiac monitoring and cardiotoxicity during adjuvant trastuzumab treatment for breast cancer: a retrospective cohort study.

CMAJ open

Chin-Yee NJ, Yan AT, Kumachev A, Ko D, Earle C, Tomlinson G, Trudeau ME, Krahn M, Krzyzanowska M, Pal R, Brezden-Masley C, Gavura S, Lien K, Chan K.
PMID: 27280116
CMAJ Open. 2016 Feb 18;4(1):E66-72. doi: 10.9778/cmajo.20150033. eCollection 2016.

BACKGROUND: Adjuvant trastuzumab is the standard of care for patients with HER2 overexpressing breast cancer, but use of trastuzumab may lead to cardiotoxicity. Our goal was to evaluate the relationship between hospital and physician case volume and cardiac outcomes...

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Chin-Yee NJ, Yan AT, Kumachev A, et al. Association of hospital and physician case volumes with cardiac monitoring and cardiotoxicity during adjuvant trastuzumab treatment for breast cancer: a retrospective cohort study. CMAJ Open. 2016;4(1):E66-72doi: 10.9778/cmajo.20150033.
Chin-Yee, N. J., Yan, A. T., Kumachev, A., Ko, D., Earle, C., Tomlinson, G., Trudeau, M. E., Krahn, M., Krzyzanowska, M., Pal, R., Brezden-Masley, C., Gavura, S., Lien, K., & Chan, K. (2016). Association of hospital and physician case volumes with cardiac monitoring and cardiotoxicity during adjuvant trastuzumab treatment for breast cancer: a retrospective cohort study. CMAJ open, 4(1), E66-72. https://doi.org/10.9778/cmajo.20150033
Chin-Yee, Nicolas J, et al. "Association of hospital and physician case volumes with cardiac monitoring and cardiotoxicity during adjuvant trastuzumab treatment for breast cancer: a retrospective cohort study." CMAJ open vol. 4,1 (2016): E66-72. doi: https://doi.org/10.9778/cmajo.20150033
Chin-Yee NJ, Yan AT, Kumachev A, Ko D, Earle C, Tomlinson G, Trudeau ME, Krahn M, Krzyzanowska M, Pal R, Brezden-Masley C, Gavura S, Lien K, Chan K. Association of hospital and physician case volumes with cardiac monitoring and cardiotoxicity during adjuvant trastuzumab treatment for breast cancer: a retrospective cohort study. CMAJ Open. 2016 Feb 18;4(1):E66-72. doi: 10.9778/cmajo.20150033. eCollection 2016. PMID: 27280116; PMCID: PMC4866921.
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Role of hydrogen-bonding and its interplay with octahedral tilting in CH3NH3PbI3.

Chemical communications (Cambridge, England)

Lee JH, Bristowe NC, Bristowe PD, Cheetham AK.
PMID: 25766075
Chem Commun (Camb). 2015 Apr 14;51(29):6434-7. doi: 10.1039/c5cc00979k.

First principles calculations on the hybrid perovskite CH3NH3PbI3 predict strong hydrogen-bonding which influences the structure and dynamics of the methylammonium cation and reveal its interaction with the tilting of the PbI6 octahedra. The calculated atomic coordinates are in excellent...

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Lee JH, Bristowe NC, Bristowe PD, et al. Role of hydrogen-bonding and its interplay with octahedral tilting in CH3NH3PbI3. Chem Commun (Camb). 2015;51(29):6434-7doi: 10.1039/c5cc00979k.
Lee, J. H., Bristowe, N. C., Bristowe, P. D., & Cheetham, A. K. (2015). Role of hydrogen-bonding and its interplay with octahedral tilting in CH3NH3PbI3. Chemical communications (Cambridge, England), 51(29), 6434-7. https://doi.org/10.1039/c5cc00979k
Lee, Jung-Hoon, et al. "Role of hydrogen-bonding and its interplay with octahedral tilting in CH3NH3PbI3." Chemical communications (Cambridge, England) vol. 51,29 (2015): 6434-7. doi: https://doi.org/10.1039/c5cc00979k
Lee JH, Bristowe NC, Bristowe PD, Cheetham AK. Role of hydrogen-bonding and its interplay with octahedral tilting in CH3NH3PbI3. Chem Commun (Camb). 2015 Apr 14;51(29):6434-7. doi: 10.1039/c5cc00979k. PMID: 25766075.
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Chemical control of the viscoelastic properties of vinylogous urethane vitrimers.

Nature communications

Denissen W, Droesbeke M, Nicolaÿ R, Leibler L, Winne JM, Du Prez FE.
PMID: 28317893
Nat Commun. 2017 Mar 20;8:14857. doi: 10.1038/ncomms14857.

Vinylogous urethane based vitrimers are polymer networks that have the intrinsic property to undergo network rearrangements, stress relaxation and viscoelastic flow, mediated by rapid addition/elimination reactions of free chain end amines. Here we show that the covalent exchange kinetics...

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Denissen W, Droesbeke M, Nicolaÿ R, et al. Chemical control of the viscoelastic properties of vinylogous urethane vitrimers. Nat Commun. 2017;8:14857doi: 10.1038/ncomms14857.
Denissen, W., Droesbeke, M., Nicolaÿ, R., Leibler, L., Winne, J. M., & Du Prez, F. E. (2017). Chemical control of the viscoelastic properties of vinylogous urethane vitrimers. Nature communications, 814857. https://doi.org/10.1038/ncomms14857
Denissen, Wim, et al. "Chemical control of the viscoelastic properties of vinylogous urethane vitrimers." Nature communications vol. 8 (2017): 14857. doi: https://doi.org/10.1038/ncomms14857
Denissen W, Droesbeke M, Nicolaÿ R, Leibler L, Winne JM, Du Prez FE. Chemical control of the viscoelastic properties of vinylogous urethane vitrimers. Nat Commun. 2017 Mar 20;8:14857. doi: 10.1038/ncomms14857. PMID: 28317893; PMCID: PMC5364391.
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Robust and Elastic Lunar and Martian Structures from 3D-Printed Regolith Inks.

Scientific reports

Jakus AE, Koube KD, Geisendorfer NR, Shah RN.
PMID: 28317904
Sci Rep. 2017 Mar 20;7:44931. doi: 10.1038/srep44931.

Here, we present a comprehensive approach for creating robust, elastic, designer Lunar and Martian regolith simulant (LRS and MRS, respectively) architectures using ambient condition, extrusion-based 3D-printing of regolith simulant inks. The LRS and MRS powders are characterized by distinct,...

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Jakus AE, Koube KD, Geisendorfer NR, et al. Robust and Elastic Lunar and Martian Structures from 3D-Printed Regolith Inks. Sci Rep. 2017;7:44931doi: 10.1038/srep44931.
Jakus, A. E., Koube, K. D., Geisendorfer, N. R., & Shah, R. N. (2017). Robust and Elastic Lunar and Martian Structures from 3D-Printed Regolith Inks. Scientific reports, 744931. https://doi.org/10.1038/srep44931
Jakus, Adam E, et al. "Robust and Elastic Lunar and Martian Structures from 3D-Printed Regolith Inks." Scientific reports vol. 7 (2017): 44931. doi: https://doi.org/10.1038/srep44931
Jakus AE, Koube KD, Geisendorfer NR, Shah RN. Robust and Elastic Lunar and Martian Structures from 3D-Printed Regolith Inks. Sci Rep. 2017 Mar 20;7:44931. doi: 10.1038/srep44931. PMID: 28317904; PMCID: PMC5357966.
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Showing 25 to 36 of 5914 entries