Zobrazeno 1 - 10
of 60
pro vyhledávání: '"John Jacobus"'
Publikováno v:
The Journal of Organic Chemistry. 45:3088-3096
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::640cdf2973894f9afa7ed3518b4b88a4
https://doi.org/10.1021/jo01303a031
https://doi.org/10.1021/jo01303a031
Autor:
Donna Hindman, John Jacobus
Publikováno v:
Tetrahedron Letters. 15:1619-1622
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a63fa9d93b9467c7a1dfdc58dd619daa
https://doi.org/10.1016/s0040-4039(01)82535-1
https://doi.org/10.1016/s0040-4039(01)82535-1
Publikováno v:
Biochemistry. 14:735-742
Torsion about the glycosidic linkage in nicotinamide mononucleotide has been investigated by quantitative application of the nuclear Overhauser effect. These measurements show that the syn (chi congruent to 20 degrees) and anti (chi congruent to 200
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::512e45a5c33219ac71698578dbf6db2f
https://doi.org/10.1021/bi00675a014
https://doi.org/10.1021/bi00675a014
Autor:
J. E. Leibner, John. Jacobus
Publikováno v:
The Journal of Physical Chemistry. 81:130-135
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::275817c4cd81d306c2d8875d62f45d4a
https://doi.org/10.1021/j100517a008
https://doi.org/10.1021/j100517a008
Publikováno v:
Proceedings of the National Academy of Sciences. 75:1227-1231
The spin-labeled cardiolipin 1-(3-sn-phosphatidyl)-3-[1-acyl-2-(16-doxylstearoyl)glycero(3)phosphol]-sn-glycerol has been prepared. The stereoselective synthesis makes use of the monolysocardiolipin 1-(3-sn-phosphatidyl)-3-[1-acyl-2-lyso-sn-glycero(3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c2d1578dabf471c466f0e217f91a34f
https://doi.org/10.1073/pnas.75.3.1227
https://doi.org/10.1073/pnas.75.3.1227
Autor:
Brenda J. Little, John Jacobus
Publikováno v:
Organic Geochemistry. 8:27-33
13 C solid-phase NMR and pyrolysis-chemical ionization mass spectrometry were used to characterize adsorbed organic material isolated on an XAD-2 macroreticular resin. Pyrolysis-chemical ionization mass spectrometry was used directly to fingerprint t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ea5ff9611da37b1a7b725749c4daf358
https://doi.org/10.1016/0146-6380(85)90047-6
https://doi.org/10.1016/0146-6380(85)90047-6
Publikováno v:
Journal of Magnetic Resonance (1969). 33:177-182
The deuteron quadrupole coupling constants (QD's) have been determined for a mixture of isomeric monodeuterocyclohexenes (containing a low level of 13C enrichment in the CD bonds) from the 2H NMR spectrum in nematic phase. The measured QD's are: 213.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20dfde285ec708a2587f8d916b867656
https://doi.org/10.1016/0022-2364(79)90201-4
https://doi.org/10.1016/0022-2364(79)90201-4
Publikováno v:
The Journal of Organic Chemistry. 44:1585-1589
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::50de40e9bf6ef6d64f09d4bb7c89f362
https://doi.org/10.1021/jo01324a001
https://doi.org/10.1021/jo01324a001
Publikováno v:
The Journal of Chemical Physics. 66:4226-4230
Measurements of the orientation parameters of a 13C enriched sample of CDH2I in nematic solvent employing 1H, 2H, and 13C NMR are reported. These parameters denoted as SCH, SCD, SHH, and SHD, obey the following relation which assumes mirror plane sym
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b087ac3d8784e197dcdc81692d466f4c
https://doi.org/10.1063/1.434497
https://doi.org/10.1063/1.434497
Autor:
Nilanjan Chakrabarti, John Jacobus
Publikováno v:
Macromolecules. 21:3011-3014
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b76d14d80d16e9e2c5006e5819acff1f
https://doi.org/10.1021/ma00188a020
https://doi.org/10.1021/ma00188a020