Výsledky vyhledávání - "W. J. HORTON"

Molecular dynamics of 1-decanol in solution studied by NMR coupled relaxation and stochastic dynamic simulations

Autor: David M. Grant, Tian Xiang. Xiang, Charles L. Mayne, W. J. Horton, Fang Liu

Publikováno v: Journal of the American Chemical Society. 114:5281-5294

The isotopic 13 C labeled 1-decanols at positions 1, 5, and 9 have been synthesized and their dynamics in (CD 3 O-CD 2 CD 2 ) 2 O, CD 3 CD 2 OD, and CD 2 Cl 2 solvents have been studied by 13 C-coupled relaxation methods. The experiments were perform

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::6f1b86ef02a5fcdae2bd4cb364f875c6
https://doi.org/10.1021/ja00039a045

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Delayed behavioural aging and altered mortality in Drosophila beta integrin mutants

Autor: M M, Goddeeris, E, Cook-Wiens, W J, Horton, H, Wolf, J R, Stoltzfus, M, Borrusch, M S, Grotewiel

Publikováno v: Aging cell. 2(5)

The genetic basis for aging is being intensely investigated in a variety of model systems. Much of the focus in Drosophila has been on the molecular-genetic determinants of lifespan, whereas the molecular-genetic basis for age-related functional decl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::0bb31554de134c0f0053d6ad0f7d4a0a
https://pubmed.ncbi.nlm.nih.gov/14570233

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Carbon-13 magnetic resonance of hydroaromatics. II. Conformation of Tetralin and tetrahydroanthracene and their methyl derivatives

Autor: Ronald J. Pugmire, Frederick G. Morin, W. J. Horton, Don K. Dalling, David M. Grant

Publikováno v: Journal of the American Chemical Society. 105:3992-3998

Carbon-13 chemical shift data have been acquired for 36 methylated tetralins and tetrahydroanthracenes. A least-squares regression analysis has been undertaken on the ring carbons of compounds of unequivocal conformation to determine methyl substitue

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::64db6525ad0fc792a9e09816f152eb3e
https://doi.org/10.1021/ja00350a042

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Solution and solid carbon-13 magnetic resonance study of the conformation of 9,10-dihydroanthracene and its 9,10-methylated derivatives

Autor: Don K. Dalling, David M. Grant, K.W. Zilm, W. J. Horton, W. A. Heeschen, Ronald J. Pugmire

Publikováno v: Journal of the American Chemical Society. 103:4817-4824

The /sup 13/C NMR chemical shifts of the 9,10-methylated 9,10-dihydroanthracenes have been obtained, both in the traditional manner in solution and in the solid state by use of cross polarization and magic angle spinning techniques. In addition, the

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::3537f3b553f17ca479ae3faa8c1f4abc
https://doi.org/10.1021/ja00406a025

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Carbon-13 magnetic resonance of hydroaromatics. 3. Conformation of 1,2,3,4-tetrahydrophenanthrene and 9,10-dihydrophenanthrene and their methyl derivatives

Autor: Don K. Dalling, W. J. Horton, David M. Grant, Frederick G. Morin, Ronald J. Pugmire

Publikováno v: The Journal of Organic Chemistry. 50:3380-3388

/sup 13/C chemical shift data have been obtained for 27 methylated 1,2,3,4-tetrahydro- and 9,10-dihydrophenanthrenes. It has been found that methyl-substituent parameters previously determined for the saturated ring of tetralin and 1,2,3,4-tetrahydro

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::5ffec40926c51aeb13c6b486370b87c0
https://doi.org/10.1021/jo00218a027

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Carbon 13 NMR study of nonenzymatic reactions of pyridoxal 5'-phosphate with selected amino acids and of related reactions

Autor: D M Grant, R D Sagers, W J Horton, D K Dalling

Publikováno v: Journal of Biological Chemistry. 251:7661-7668

Carbon 13 nuclear magnetic resonance spectroscopy has been used to monitor the nonenzymatic reactions of pyridoxal 5'-phosphate with glycine, alanine, valine, serine, and with several other model compounds. Isotopically enriched amino acids were empl

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::50a739d018f8c7f3476597503e4607c7
https://doi.org/10.1016/s0021-9258(17)32903-4

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