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A sequential timing device.

Research quarterly

Windell EJ, Kindig LE.
PMID: 1059216
Res Q. 1975 Oct;46(3):391.

No abstract available.

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Windell EJ, Kindig LE. A sequential timing device. Res Q. 1975;46(3):391
Windell, E. J., & Kindig, L. E. (1975). A sequential timing device. Research quarterly, 46(3), 391.
Windell, E J, and Kindig, L E. "A sequential timing device." Research quarterly vol. 46,3 (1975): 391.
Windell EJ, Kindig LE. A sequential timing device. Res Q. 1975 Oct;46(3):391. PMID: 1059216.
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Maternal Education and the Link between Birth Timing and Children's School Readiness.

Social science quarterly

Augustine J, Prickett KC, Kendig S, Crosnoe R.
PMID: 27199499
Soc Sci Q. 2015 Dec;96(4):970-984. doi: 10.1111/ssqu.12150. Epub 2015 Apr 17.

OBJECTIVE: This study explored whether mothers' education magnified the benefits of their fertility delays for their children.METHODS: Multiple-group path modeling assessed whether and why the positive association between mothers' age at first birth and children's test scores was greater...

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Augustine J, Prickett KC, Kendig S, et al. Maternal Education and the Link between Birth Timing and Children's School Readiness. Soc Sci Q. 2015;96(4):970-984doi: 10.1111/ssqu.12150.
Augustine, J., Prickett, K. C., Kendig, S., & Crosnoe, R. (2015). Maternal Education and the Link between Birth Timing and Children's School Readiness. Social science quarterly, 96(4), 970-984. https://doi.org/10.1111/ssqu.12150
Augustine, Jennifer, et al. "Maternal Education and the Link between Birth Timing and Children's School Readiness." Social science quarterly vol. 96,4 (2015): 970-984. doi: https://doi.org/10.1111/ssqu.12150
Augustine J, Prickett KC, Kendig S, Crosnoe R. Maternal Education and the Link between Birth Timing and Children's School Readiness. Soc Sci Q. 2015 Dec;96(4):970-984. doi: 10.1111/ssqu.12150. Epub 2015 Apr 17. PMID: 27199499; PMCID: PMC4868183.
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Response.

The Journal of the American Osteopathic Association

Hensel KL, Roane BM, Smith-Barbaro P.
PMID: 28459479
J Am Osteopath Assoc. 2017 May 01;117(5):290. doi: 10.7556/jaoa.2017.051.

No abstract available.

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Hensel KL, Roane BM, Smith-Barbaro P. Response. J Am Osteopath Assoc. 2017;117(5):290doi: 10.7556/jaoa.2017.051.
Hensel, K. L., Roane, B. M., & Smith-Barbaro, P. (2017). Response. The Journal of the American Osteopathic Association, 117(5), 290. https://doi.org/10.7556/jaoa.2017.051
Hensel, Kendi L, et al. "Response." The Journal of the American Osteopathic Association vol. 117,5 (2017): 290. doi: https://doi.org/10.7556/jaoa.2017.051
Hensel KL, Roane BM, Smith-Barbaro P. Response. J Am Osteopath Assoc. 2017 May 01;117(5):290. doi: 10.7556/jaoa.2017.051. PMID: 28459479.
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Medical Care for Swimmers.

Sports medicine - open

Khodaee M, Edelman GT, Spittler J, Wilber R, Krabak BJ, Solomon D, Riewald S, Kendig A, Borgelt LM, Riederer M, Puzovic V, Rodeo S.
PMID: 27512647
Sports Med Open. 2016 Jul 25;2:27. doi: 10.1186/s40798-016-0051-2. eCollection 2015 Jun.

Swimming is one of the most popular sports worldwide. Competitive swimming is one of the most watched sports during the Olympic Games. Swimming has unique medical challenges as a result of a variety of environmental and chemical exposures. Musculoskeletal...

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Khodaee M, Edelman GT, Spittler J, et al. Medical Care for Swimmers. Sports Med Open. 2016;2:27doi: 10.1186/s40798-016-0051-2.
Khodaee, M., Edelman, G. T., Spittler, J., Wilber, R., Krabak, B. J., Solomon, D., Riewald, S., Kendig, A., Borgelt, L. M., Riederer, M., Puzovic, V., & Rodeo, S. (2015). Medical Care for Swimmers. Sports medicine - open, 227. https://doi.org/10.1186/s40798-016-0051-2
Khodaee, Morteza, et al. "Medical Care for Swimmers." Sports medicine - open vol. 2 (2015): 27. doi: https://doi.org/10.1186/s40798-016-0051-2
Khodaee M, Edelman GT, Spittler J, Wilber R, Krabak BJ, Solomon D, Riewald S, Kendig A, Borgelt LM, Riederer M, Puzovic V, Rodeo S. Medical Care for Swimmers. Sports Med Open. 2016 Jul 25;2:27. doi: 10.1186/s40798-016-0051-2. eCollection 2015 Jun. PMID: 27512647; PMCID: PMC4960281.
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Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent.

Chemical communications (Cambridge, England)

Praz J, Graff J, Egger L, Guénée L, Wagschal S, Kündig EP, Alexakis A.
PMID: 26439116
Chem Commun (Camb). 2015 Dec 11;51(95):16912-5. doi: 10.1039/c5cc06548h.

The asymmetric bromine-lithium exchange on a series of prochiral biphenyls was investigated. As in many asymmetric organolithium reactions, the chiral ligand (here a diamine) was considered to be the enantiocontrolling element. We show here that the organolithium reagent also...

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Praz J, Graff J, Egger L, et al. Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent. Chem Commun (Camb). 2015;51(95):16912-5doi: 10.1039/c5cc06548h.
Praz, J., Graff, J., Egger, L., Guénée, L., Wagschal, S., Kündig, E. P., & Alexakis, A. (2015). Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent. Chemical communications (Cambridge, England), 51(95), 16912-5. https://doi.org/10.1039/c5cc06548h
Praz, Jézabel, et al. "Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent." Chemical communications (Cambridge, England) vol. 51,95 (2015): 16912-5. doi: https://doi.org/10.1039/c5cc06548h
Praz J, Graff J, Egger L, Guénée L, Wagschal S, Kündig EP, Alexakis A. Asymmetric bromine-lithium exchange: on the importance of both the diamine ligand and the organolithium reagent. Chem Commun (Camb). 2015 Dec 11;51(95):16912-5. doi: 10.1039/c5cc06548h. PMID: 26439116.
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[CpRu((R)-Binop-F)(H2O)][SbF6], a new fluxional chiral Lewis acid catalyst: synthesis, dynamic nmr, asymmetric catalysis, and theoretical studies.

Journal of the American Chemical Society

Alezra V, Bernardinelli G, Corminboeuf C, Frey U, Kündig EP, Merbach AE, Saudan CM, Viton F, Weber J.
PMID: 15080688
J Am Chem Soc. 2004 Apr 21;126(15):4843-53. doi: 10.1021/ja0374123.

The C(2)-symmetric electron-poor ligand (R)-BINOP-F (4) was prepared by reaction of (R)-BINOL with bis(pentafluorophenyl)-phosphorus bromide in the presence of triethylamine. The iodo complex [CpRu((R)-BINOP-F)(I)] ((R)-6) was obtained by substitution of two carbonyl ligands by (R)-4 in the in situ-prepared...

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Alezra V, Bernardinelli G, Corminboeuf C, et al. [CpRu((R)-Binop-F)(H2O)][SbF6], a new fluxional chiral Lewis acid catalyst: synthesis, dynamic nmr, asymmetric catalysis, and theoretical studies. J Am Chem Soc. 2004;126(15):4843-53doi: 10.1021/ja0374123.
Alezra, V., Bernardinelli, G., Corminboeuf, C., Frey, U., Kündig, E. P., Merbach, A. E., Saudan, C. M., Viton, F., & Weber, J. (2004). [CpRu((R)-Binop-F)(H2O)][SbF6], a new fluxional chiral Lewis acid catalyst: synthesis, dynamic nmr, asymmetric catalysis, and theoretical studies. Journal of the American Chemical Society, 126(15), 4843-53. https://doi.org/10.1021/ja0374123
Alezra, Valérie, et al. "[CpRu((R)-Binop-F)(H2O)][SbF6], a new fluxional chiral Lewis acid catalyst: synthesis, dynamic nmr, asymmetric catalysis, and theoretical studies." Journal of the American Chemical Society vol. 126,15 (2004): 4843-53. doi: https://doi.org/10.1021/ja0374123
Alezra V, Bernardinelli G, Corminboeuf C, Frey U, Kündig EP, Merbach AE, Saudan CM, Viton F, Weber J. [CpRu((R)-Binop-F)(H2O)][SbF6], a new fluxional chiral Lewis acid catalyst: synthesis, dynamic nmr, asymmetric catalysis, and theoretical studies. J Am Chem Soc. 2004 Apr 21;126(15):4843-53. doi: 10.1021/ja0374123. PMID: 15080688.
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Chemosensory performance of molecularly imprinted fluorescent conjugated polymer materials.

Journal of the American Chemical Society

Li J, Kendig CE, Nesterov EE.
PMID: 18044891
J Am Chem Soc. 2007 Dec 26;129(51):15911-8. doi: 10.1021/ja0748027. Epub 2007 Nov 29.

Fluorescent conjugated polymers are an attractive basis for the design of low detection limit sensing devices owing to their intrinsic signal amplification capability. A simple and universal method to rationally control or fine-tune the chemodetection selectivity of conjugated polymer...

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Li J, Kendig CE, Nesterov EE. Chemosensory performance of molecularly imprinted fluorescent conjugated polymer materials. J Am Chem Soc. 2007;129(51):15911-8doi: 10.1021/ja0748027.
Li, J., Kendig, C. E., & Nesterov, E. E. (2007). Chemosensory performance of molecularly imprinted fluorescent conjugated polymer materials. Journal of the American Chemical Society, 129(51), 15911-8. https://doi.org/10.1021/ja0748027
Li, Jiahui, et al. "Chemosensory performance of molecularly imprinted fluorescent conjugated polymer materials." Journal of the American Chemical Society vol. 129,51 (2007): 15911-8. doi: https://doi.org/10.1021/ja0748027
Li J, Kendig CE, Nesterov EE. Chemosensory performance of molecularly imprinted fluorescent conjugated polymer materials. J Am Chem Soc. 2007 Dec 26;129(51):15911-8. doi: 10.1021/ja0748027. Epub 2007 Nov 29. PMID: 18044891.
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Tuberculosis in infancy and childhood.

Virginia medical monthly

KENDIG EL.
PMID: 13039265
Va Med Mon (1918). 1953 Mar;80(3):157-8.

No abstract available.

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KENDIG EL. Tuberculosis in infancy and childhood. Va Med Mon (1918). 1953;80(3):157-8
KENDIG, E. L. (1953). Tuberculosis in infancy and childhood. Virginia medical monthly, 80(3), 157-8.
KENDIG, E L. "Tuberculosis in infancy and childhood." Virginia medical monthly vol. 80,3 (1953): 157-8.
KENDIG EL. Tuberculosis in infancy and childhood. Va Med Mon (1918). 1953 Mar;80(3):157-8. PMID: 13039265.
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Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts.

Chemical communications (Cambridge, England)

Kündig EP, Lomberget T, Bragg R, Poulard C, Bernardinelli G.
PMID: 15216374
Chem Commun (Camb). 2004 Jul 07;(13):1548-9. doi: 10.1039/b404006f. Epub 2004 May 21.

[Cr(CO)3(naphthoquinone)](1), prepared in a three-step sequence starting from 1,4-dihydroxynaphthalene, was reduced to the corresponding meso-dihydronaphthalene syn-diol complex and the latter was desymmetrized to give the mono-acyl complex with 99% ee via asymmetric acylation catalyzed by the two new and...

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Kündig EP, Lomberget T, Bragg R, et al. Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chem Commun (Camb). 2004;(13):1548-9doi: 10.1039/b404006f.
Kündig, E. P., Lomberget, T., Bragg, R., Poulard, C., & Bernardinelli, G. (2004). Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chemical communications (Cambridge, England), (13), 1548-9. https://doi.org/10.1039/b404006f
Kündig, E Peter, et al. "Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts." Chemical communications (Cambridge, England) vol. ,13 (2004): 1548-9. doi: https://doi.org/10.1039/b404006f
Kündig EP, Lomberget T, Bragg R, Poulard C, Bernardinelli G. Desymmetrization of a meso-diol complex derived from [Cr(CO)3(eta6-5,8-naphthoquinone)]: use of new diamine acylation catalysts. Chem Commun (Camb). 2004 Jul 07;(13):1548-9. doi: 10.1039/b404006f. Epub 2004 May 21. PMID: 15216374.
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Iron- and ruthenium-Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between enals and diaryl nitrones.

Chemistry, an Asian journal

Bădoiu A, Bernardinelli G, Mareda J, Kündig EP, Viton F.
PMID: 18633952
Chem Asian J. 2008 Sep 01;3(8):1298-311. doi: 10.1002/asia.200800063.

The highly tuned, one-point binding cationic cyclopentadienyl-iron and -ruthenium complexes 1 and 2 that incorporate chiral bidentate pentafluoroaryl-phosphinite ligands selectively coordinate and activate alpha,beta-unsaturated carbonyl compounds towards asymmetric catalytic cycloaddition reactions with diaryl nitrones. The reaction gives isoxazolidine products...

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Bădoiu A, Bernardinelli G, Mareda J, et al. Iron- and ruthenium-Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between enals and diaryl nitrones. Chem Asian J. 2008;3(8):1298-311doi: 10.1002/asia.200800063.
Bădoiu, A., Bernardinelli, G., Mareda, J., Kündig, E. P., & Viton, F. (2008). Iron- and ruthenium-Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between enals and diaryl nitrones. Chemistry, an Asian journal, 3(8), 1298-311. https://doi.org/10.1002/asia.200800063
Bădoiu, Andrei, et al. "Iron- and ruthenium-Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between enals and diaryl nitrones." Chemistry, an Asian journal vol. 3,8 (2008): 1298-311. doi: https://doi.org/10.1002/asia.200800063
Bădoiu A, Bernardinelli G, Mareda J, Kündig EP, Viton F. Iron- and ruthenium-Lewis acid catalyzed asymmetric 1,3-dipolar cycloaddition reactions between enals and diaryl nitrones. Chem Asian J. 2008 Sep 01;3(8):1298-311. doi: 10.1002/asia.200800063. PMID: 18633952.
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Stereoselective dimerization of racemic C3-symmetric Ti(IV) amine triphenolate complexes.

Dalton transactions (Cambridge, England : 2003)

Bernardinelli G, Seidel TM, Kündig EP, Prins LJ, Kolarovic A, Mba M, Pontini M, Licini G.
PMID: 17426858
Dalton Trans. 2007 Apr 28;(16):1573-6. doi: 10.1039/b702958f. Epub 2007 Mar 15.

A novel, mononuclear Ti(IV) amine triphenolate complex obtained by reaction of Ti(OiPr)(4) with tris(2-hydroxy-3-phenylbenzyl)amine bearing phenyl ortho-substituents affords quantitatively and spontaneously the corresponding heterochiral micro-oxo dinuclear compound whereas an analogous chiral, enantiopure complex maintains its mononuclear structure even in...

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Bernardinelli G, Seidel TM, Kündig EP, et al. Stereoselective dimerization of racemic C3-symmetric Ti(IV) amine triphenolate complexes. Dalton Trans. 2007;(16):1573-6doi: 10.1039/b702958f.
Bernardinelli, G., Seidel, T. M., Kündig, E. P., Prins, L. J., Kolarovic, A., Mba, M., Pontini, M., & Licini, G. (2007). Stereoselective dimerization of racemic C3-symmetric Ti(IV) amine triphenolate complexes. Dalton transactions (Cambridge, England : 2003), (16), 1573-6. https://doi.org/10.1039/b702958f
Bernardinelli, Gérald, et al. "Stereoselective dimerization of racemic C3-symmetric Ti(IV) amine triphenolate complexes." Dalton transactions (Cambridge, England : 2003) vol. ,16 (2007): 1573-6. doi: https://doi.org/10.1039/b702958f
Bernardinelli G, Seidel TM, Kündig EP, Prins LJ, Kolarovic A, Mba M, Pontini M, Licini G. Stereoselective dimerization of racemic C3-symmetric Ti(IV) amine triphenolate complexes. Dalton Trans. 2007 Apr 28;(16):1573-6. doi: 10.1039/b702958f. Epub 2007 Mar 15. PMID: 17426858.
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Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis.

Organic & biomolecular chemistry

Kündig EP, Bellido A, Kaliappan KP, Pape AR, Radix S.
PMID: 16391777
Org Biomol Chem. 2006 Jan 21;4(2):342-51. doi: 10.1039/b513261d. Epub 2005 Dec 14.

cis-Fused [6,8], [6,7], [6,6] and [6,5] ring systems containing a cyclohexadiene ring unit, a cycloenone ring and a quaternary carbon at the ring junction were obtained in only two steps from [Cr(CO)3(eta6-p-methoxyphenyl oxazoline)]. The sequence proceeds via diastereoselective addition...

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Kündig EP, Bellido A, Kaliappan KP, et al. Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis. Org Biomol Chem. 2005;4(2):342-51doi: 10.1039/b513261d.
Kündig, E. P., Bellido, A., Kaliappan, K. P., Pape, A. R., & Radix, S. (2006). Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis. Organic & biomolecular chemistry, 4(2), 342-51. https://doi.org/10.1039/b513261d
Kündig, E Peter, et al. "Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis." Organic & biomolecular chemistry vol. 4,2 (2006): 342-51. doi: https://doi.org/10.1039/b513261d
Kündig EP, Bellido A, Kaliappan KP, Pape AR, Radix S. Synthesis of [6,n] cis-fused ring compounds via Cr-mediated dearomatisation-ring-closing metathesis. Org Biomol Chem. 2006 Jan 21;4(2):342-51. doi: 10.1039/b513261d. Epub 2005 Dec 14. PMID: 16391777.
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Showing 1 to 12 of 114 entries