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Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives.

Organic & biomolecular chemistry

Bawa RA, Gautier FM, Adams H, Meijer AJ, Jones S.
PMID: 26340318
Org Biomol Chem. 2015 Nov 14;13(42):10569-77. doi: 10.1039/c5ob01343g. Epub 2015 Sep 04.

Several 9-(2-aminoethyl)anthracene derivatives were prepared with different nitrogen substitutents including alkyl, acetamide, trifluoroacaeamide and t-butyl carbamate. The selectivity in Diels-Alder cyclodaddition reaction with N-methyl maleimide was evaluated through single crystal X-ray analysis of the products. Models for the change...

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Bawa RA, Gautier FM, Adams H, et al. Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Org Biomol Chem. 2015;13(42):10569-77doi: 10.1039/c5ob01343g.
Bawa, R. A., Gautier, F. M., Adams, H., Meijer, A. J., & Jones, S. (2015). Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Organic & biomolecular chemistry, 13(42), 10569-77. https://doi.org/10.1039/c5ob01343g
Bawa, R A, et al. "Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives." Organic & biomolecular chemistry vol. 13,42 (2015): 10569-77. doi: https://doi.org/10.1039/c5ob01343g
Bawa RA, Gautier FM, Adams H, Meijer AJ, Jones S. Evaluating hydrogen bonding control in the diastereoselective Diels-Alder reactions of 9-(2-aminoethyl)-anthracene derivatives. Org Biomol Chem. 2015 Nov 14;13(42):10569-77. doi: 10.1039/c5ob01343g. Epub 2015 Sep 04. PMID: 26340318.
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Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis.

Nature communications

Yang X, Keane T, Delor M, Meijer AJ, Weinstein J, Bittner ER.
PMID: 28233775
Nat Commun. 2017 Feb 24;8:14554. doi: 10.1038/ncomms14554.

We report upon an analysis of the vibrational modes that couple and drive the state-to-state electronic transfer branching ratios in a model donor-bridge-acceptor system consisting of a phenothiazine-based donor linked to a naphthalene-monoimide acceptor via a platinum-acetylide bridging unit....

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Yang X, Keane T, Delor M, et al. Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis. Nat Commun. 2017;8:14554doi: 10.1038/ncomms14554.
Yang, X., Keane, T., Delor, M., Meijer, A. J., Weinstein, J., & Bittner, E. R. (2017). Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis. Nature communications, 814554. https://doi.org/10.1038/ncomms14554
Yang, Xunmo, et al. "Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis." Nature communications vol. 8 (2017): 14554. doi: https://doi.org/10.1038/ncomms14554
Yang X, Keane T, Delor M, Meijer AJ, Weinstein J, Bittner ER. Identifying electron transfer coordinates in donor-bridge-acceptor systems using mode projection analysis. Nat Commun. 2017 Feb 24;8:14554. doi: 10.1038/ncomms14554. PMID: 28233775; PMCID: PMC5333094.
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Mechanistic insight into proton-coupled mixed valency.

Chemical communications (Cambridge, England)

Wilkinson LA, Vincent KB, Meijer AJ, Patmore NJ.
PMID: 26497070
Chem Commun (Camb). 2016 Jan 04;52(1):100-3. doi: 10.1039/c5cc07101a.

Stabilisation of the mixed-valence state in [Mo2(TiPB)3(HDOP)]2(+) (HTiPB = 2,4,6-triisopropylbenzoic acid, H2DOP = 3,6-dihydroxypyridazine) by electron transfer (ET) is related to the proton coordinate of the bridging ligands. Spectroelectrochemical studies suggest that ET is slower than 10(9) s(-1). The...

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Wilkinson LA, Vincent KB, Meijer AJ, et al. Mechanistic insight into proton-coupled mixed valency. Chem Commun (Camb). 2016;52(1):100-3doi: 10.1039/c5cc07101a.
Wilkinson, L. A., Vincent, K. B., Meijer, A. J., & Patmore, N. J. (2016). Mechanistic insight into proton-coupled mixed valency. Chemical communications (Cambridge, England), 52(1), 100-3. https://doi.org/10.1039/c5cc07101a
Wilkinson, Luke A, et al. "Mechanistic insight into proton-coupled mixed valency." Chemical communications (Cambridge, England) vol. 52,1 (2016): 100-3. doi: https://doi.org/10.1039/c5cc07101a
Wilkinson LA, Vincent KB, Meijer AJ, Patmore NJ. Mechanistic insight into proton-coupled mixed valency. Chem Commun (Camb). 2016 Jan 04;52(1):100-3. doi: 10.1039/c5cc07101a. PMID: 26497070.
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[Effectiveness of influenza vaccine in the Netherlands: predominant circulating virus type and vaccine match are important conditions].

Nederlands tijdschrift voor geneeskunde

van Doorn E, Darvishian M, Dijkstra F, Bijlsma MJ, Donker GA, de Lange MMA, Cadenau LM, Hak E, Meijer A.
PMID: 28558853
Ned Tijdschr Geneeskd. 2017;161:D1648.

OBJECTIVE: To investigate the relationship between circulating influenza virus A types and subtypes and influenza B lineages, their match with the vaccine and the effectiveness of the influenza vaccine (IVE).DESIGN: Test negative case control study.METHOD: We used data from...

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van Doorn E, Darvishian M, Dijkstra F, et al. Effectiviteit van influenzavaccinatie in Nederland. [Effectiveness of influenza vaccine in the Netherlands: predominant circulating virus type and vaccine match are important conditions]. Ned Tijdschr Geneeskd. 2017;161:D1648
van Doorn, E., Darvishian, M., Dijkstra, F., Bijlsma, M. J., Donker, G. A., de Lange, M. M. A., Cadenau, L. M., Hak, E., & Meijer, A. (2017). Effectiviteit van influenzavaccinatie in Nederland. [Effectiveness of influenza vaccine in the Netherlands: predominant circulating virus type and vaccine match are important conditions]. Nederlands tijdschrift voor geneeskunde, 161D1648.
van Doorn, E, et al. "Effectiviteit van influenzavaccinatie in Nederland." [Effectiveness of influenza vaccine in the Netherlands: predominant circulating virus type and vaccine match are important conditions]. Nederlands tijdschrift voor geneeskunde vol. 161 (2017): D1648.
van Doorn E, Darvishian M, Dijkstra F, Bijlsma MJ, Donker GA, de Lange MMA, Cadenau LM, Hak E, Meijer A. Effectiviteit van influenzavaccinatie in Nederland. [Effectiveness of influenza vaccine in the Netherlands: predominant circulating virus type and vaccine match are important conditions]. Ned Tijdschr Geneeskd. 2017;161:D1648. Dutch. PMID: 28558853.
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Intracavity OptoGalvanic Spectroscopy not suitable for ambient level radiocarbon detection.

Analytical chemistry

Paul D, Meijer HA.
PMID: 26252648
Anal Chem. 2015 Sep 01;87(17):9025-32. doi: 10.1021/acs.analchem.5b02226. Epub 2015 Aug 13.

IntraCavity OptoGalvanic Spectroscopy as a radiocarbon detection technique was first reported by the Murnick group at Rutgers University, Newark, NJ, in 2008. This technique for radiocarbon detection was presented with tremendous potentials for applications in various fields of research....

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Paul D, Meijer HA. Intracavity OptoGalvanic Spectroscopy not suitable for ambient level radiocarbon detection. Anal Chem. 2015;87(17):9025-32doi: 10.1021/acs.analchem.5b02226.
Paul, D., & Meijer, H. A. (2015). Intracavity OptoGalvanic Spectroscopy not suitable for ambient level radiocarbon detection. Analytical chemistry, 87(17), 9025-32. https://doi.org/10.1021/acs.analchem.5b02226
Paul, Dipayan, and Meijer, Harro A J. "Intracavity OptoGalvanic Spectroscopy not suitable for ambient level radiocarbon detection." Analytical chemistry vol. 87,17 (2015): 9025-32. doi: https://doi.org/10.1021/acs.analchem.5b02226
Paul D, Meijer HA. Intracavity OptoGalvanic Spectroscopy not suitable for ambient level radiocarbon detection. Anal Chem. 2015 Sep 01;87(17):9025-32. doi: 10.1021/acs.analchem.5b02226. Epub 2015 Aug 13. PMID: 26252648.
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Correction to online hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high-temperature elemental-analyzer techniques.

Analytical chemistry

Gehre M, Renpenning J, Gilevska T, Qi H, Coplen TB, Meijer HA, Brand WA, Schimmelmann A.
PMID: 26284431
Anal Chem. 2015 Sep 01;87(17):9108. doi: 10.1021/acs.analchem.5b03098. Epub 2015 Aug 18.

No abstract available.

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Gehre M, Renpenning J, Gilevska T, et al. Correction to online hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high-temperature elemental-analyzer techniques. Anal Chem. 2015;87(17):9108doi: 10.1021/acs.analchem.5b03098.
Gehre, M., Renpenning, J., Gilevska, T., Qi, H., Coplen, T. B., Meijer, H. A., Brand, W. A., & Schimmelmann, A. (2015). Correction to online hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high-temperature elemental-analyzer techniques. Analytical chemistry, 87(17), 9108. https://doi.org/10.1021/acs.analchem.5b03098
Gehre, Matthias, et al. "Correction to online hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high-temperature elemental-analyzer techniques." Analytical chemistry vol. 87,17 (2015): 9108. doi: https://doi.org/10.1021/acs.analchem.5b03098
Gehre M, Renpenning J, Gilevska T, Qi H, Coplen TB, Meijer HA, Brand WA, Schimmelmann A. Correction to online hydrogen-isotope measurements of organic samples using elemental chromium: an extension for high-temperature elemental-analyzer techniques. Anal Chem. 2015 Sep 01;87(17):9108. doi: 10.1021/acs.analchem.5b03098. Epub 2015 Aug 18. PMID: 26284431.
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Simulation and virtual reality in surgical education: real or unreal?.

Archives of surgery (Chicago, Ill. : 1960)

Gorman PJ, Meier AH, Krummel TM.
PMID: 10555634
Arch Surg. 1999 Nov;134(11):1203-8. doi: 10.1001/archsurg.134.11.1203.

Rapid change is under way on several fronts in medicine and surgery. Advances in computing power have enabled continued growth in virtual reality, visualization, and simulation technologies. The ideal learning opportunities afforded by simulated and virtual environments have prompted...

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Gorman PJ, Meier AH, Krummel TM. Simulation and virtual reality in surgical education: real or unreal?. Arch Surg. 1999;134(11):1203-8doi: 10.1001/archsurg.134.11.1203.
Gorman, P. J., Meier, A. H., & Krummel, T. M. (1999). Simulation and virtual reality in surgical education: real or unreal?. Archives of surgery (Chicago, Ill. : 1960), 134(11), 1203-8. https://doi.org/10.1001/archsurg.134.11.1203
Gorman, P J, et al. "Simulation and virtual reality in surgical education: real or unreal?." Archives of surgery (Chicago, Ill. : 1960) vol. 134,11 (1999): 1203-8. doi: https://doi.org/10.1001/archsurg.134.11.1203
Gorman PJ, Meier AH, Krummel TM. Simulation and virtual reality in surgical education: real or unreal?. Arch Surg. 1999 Nov;134(11):1203-8. doi: 10.1001/archsurg.134.11.1203. PMID: 10555634.
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Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities.

The Journal of organic chemistry

Beijer FH, Sijbesma RP, Vekemans JA, Meijer EW, Kooijman H, Spek AL.
PMID: 11667479
J Org Chem. 1996 Sep 06;61(18):6371-6380. doi: 10.1021/jo960612v.

The association behavior of several 2,4-diamino-s-triazines, 2,6-diaminopyridines, and their acylated derivatives with uracil derivatives was studied. In solution (1)H-NMR and IR spectroscopy were used, and in the solid state as (co)crystals X-ray diffraction was used. Acylation of 2,6-diaminopyridine leads...

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Beijer FH, Sijbesma RP, Vekemans JA, et al. Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. J Org Chem. 1996;61(18):6371-6380doi: 10.1021/jo960612v.
Beijer, F. H., Sijbesma, R. P., Vekemans, J. A., Meijer, E. W., Kooijman, H., & Spek, A. L. (1996). Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. The Journal of organic chemistry, 61(18), 6371-6380. https://doi.org/10.1021/jo960612v
Beijer, Felix H., et al. "Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities." The Journal of organic chemistry vol. 61,18 (1996): 6371-6380. doi: https://doi.org/10.1021/jo960612v
Beijer FH, Sijbesma RP, Vekemans JA, Meijer EW, Kooijman H, Spek AL. Hydrogen-Bonded Complexes of Diaminopyridines and Diaminotriazines: Opposite Effect of Acylation on Complex Stabilities. J Org Chem. 1996 Sep 06;61(18):6371-6380. doi: 10.1021/jo960612v. PMID: 11667479.
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Computer-assisted training and learning in surgery.

Computer aided surgery : official journal of the International Society for Computer Aided Surgery

Gorman PJ, Meier AH, Krummel TM.
PMID: 10862134
Comput Aided Surg. 2000;5(2):120-30. doi: 10.1002/1097-0150(2000)5:2<120::AID-IGS6>3.0.CO;2-L.

The teaching and learning of surgery is a time-honored tradition based upon the "see one, do one, teach one" apprenticeship model. Recent improvement of this model has centered upon incremental change in skills teaching and testing and curricular development....

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Gorman PJ, Meier AH, Krummel TM. Computer-assisted training and learning in surgery. Comput Aided Surg. 2000;5(2):120-30doi: 10.1002/1097-0150(2000)5:2<120::AID-IGS6>3.0.CO;2-L.
Gorman, P. J., Meier, A. H., & Krummel, T. M. (2000). Computer-assisted training and learning in surgery. Computer aided surgery : official journal of the International Society for Computer Aided Surgery, 5(2), 120-30. https://doi.org/10.1002/1097-0150(2000)5:2<120::AID-IGS6>3.0.CO;2-L
Gorman, P J, et al. "Computer-assisted training and learning in surgery." Computer aided surgery : official journal of the International Society for Computer Aided Surgery vol. 5,2 (2000): 120-30. doi: https://doi.org/10.1002/1097-0150(2000)5:2<120::AID-IGS6>3.0.CO;2-L
Gorman PJ, Meier AH, Krummel TM. Computer-assisted training and learning in surgery. Comput Aided Surg. 2000;5(2):120-30. doi: 10.1002/1097-0150(2000)5:2<120::AID-IGS6>3.0.CO;2-L. PMID: 10862134.
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Glucose 6-phosphate compartmentation and the control of glycogen synthesis.

Journal of hepatology

Meijer A.
PMID: 12175643
J Hepatol. 2002 Sep;37(3):417. doi: 10.1016/s0168-8278(02)00166-6.

No abstract available.

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Meijer A. Glucose 6-phosphate compartmentation and the control of glycogen synthesis. J Hepatol. 2002;37(3):417doi: 10.1016/s0168-8278(02)00166-6.
Meijer, A. (2002). Glucose 6-phosphate compartmentation and the control of glycogen synthesis. Journal of hepatology, 37(3), 417. https://doi.org/10.1016/s0168-8278(02)00166-6
Meijer, Alfred. "Glucose 6-phosphate compartmentation and the control of glycogen synthesis." Journal of hepatology vol. 37,3 (2002): 417. doi: https://doi.org/10.1016/s0168-8278(02)00166-6
Meijer A. Glucose 6-phosphate compartmentation and the control of glycogen synthesis. J Hepatol. 2002 Sep;37(3):417. doi: 10.1016/s0168-8278(02)00166-6. PMID: 12175643.
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A Suzuki coupling based route to 2,2'-bis(2-indenyl)biphenyl derivatives.

The Journal of organic chemistry

IJpeij EG, Beijer FH, Arts HJ, Newton C, de Vries JG, Gruter GJ.
PMID: 11777455
J Org Chem. 2002 Jan 11;67(1):169-76. doi: 10.1021/jo016040i.

Because of the promising performance in olefin polymerization of 2,2'-bis(2-indenyldiyl)biphenyl zirconium dichloride, we developed a new and broadly applicable route to 2,2'-bis(2-indenyl)biphenyl derivatives. Reaction of the known 2,2'-diiodobiphenyl (26) with the new 2-indenyl boronic acid (23) did not result...

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IJpeij EG, Beijer FH, Arts HJ, et al. A Suzuki coupling based route to 2,2'-bis(2-indenyl)biphenyl derivatives. J Org Chem. 2002;67(1):169-76doi: 10.1021/jo016040i.
IJpeij, E. G., Beijer, F. H., Arts, H. J., Newton, C., de Vries, J. G., & Gruter, G. J. (2002). A Suzuki coupling based route to 2,2'-bis(2-indenyl)biphenyl derivatives. The Journal of organic chemistry, 67(1), 169-76. https://doi.org/10.1021/jo016040i
IJpeij, Edwin G, et al. "A Suzuki coupling based route to 2,2'-bis(2-indenyl)biphenyl derivatives." The Journal of organic chemistry vol. 67,1 (2002): 169-76. doi: https://doi.org/10.1021/jo016040i
IJpeij EG, Beijer FH, Arts HJ, Newton C, de Vries JG, Gruter GJ. A Suzuki coupling based route to 2,2'-bis(2-indenyl)biphenyl derivatives. J Org Chem. 2002 Jan 11;67(1):169-76. doi: 10.1021/jo016040i. PMID: 11777455.
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Standards for the Ph.D. Degree in the Molecular Biosciences.

Biochemical education

Vella F, de Meis L, Mehler AH, Rombauts W, White HB, Wood EJ.
PMID: 10717446
Biochem Educ. 2000 Jan 01;28(1):2-11. doi: 10.1016/s0307-4412(99)00123-5.

No abstract available.

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Vella F, de Meis L, Mehler AH, et al. Standards for the Ph.D. Degree in the Molecular Biosciences. Biochem Educ. 2000;28(1):2-11doi: 10.1016/s0307-4412(99)00123-5.
Vella, F., de Meis L, Mehler, A. H., Rombauts, W., White, H. B., & Wood, E. J. (2000). Standards for the Ph.D. Degree in the Molecular Biosciences. Biochemical education, 28(1), 2-11. https://doi.org/10.1016/s0307-4412(99)00123-5
Vella, et al. "Standards for the Ph.D. Degree in the Molecular Biosciences." Biochemical education vol. 28,1 (2000): 2-11. doi: https://doi.org/10.1016/s0307-4412(99)00123-5
Vella F, de Meis L, Mehler AH, Rombauts W, White HB, Wood EJ. Standards for the Ph.D. Degree in the Molecular Biosciences. Biochem Educ. 2000 Jan 01;28(1):2-11. doi: 10.1016/s0307-4412(99)00123-5. PMID: 10717446.
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Showing 1 to 12 of 255 entries