Zobrazeno 1 - 7
of 7
pro vyhledávání: '"David Whittern"'
Autor:
Stephen G, Spanton, David, Whittern
Publikováno v:
Magnetic resonance in chemistry : MRC. 47(12)
We have developed an NMR chemical shift prediction system that enables high throughput automatic grading of NMR spectra. In support of high throughput synthetic efforts for our drug discovery program, a rapid and accurate analysis for identity was ne
Autor:
John Hengeveld, Jack Tadanier, William Rosenbrook, David Whittern, Cheuk-Man Lee, Norman Wideburg
Publikováno v:
Carbohydrate Research. 201:209-222
Analogs of 3-deoxy- d - manno -octulosonic acid (Kdo) having the β-anomeric hydroxyl group replaced by a substituted-methyl group were prepared from Kdo. The substituted-methyl groups were derived from the carboxyl group of Kdo, whereas the carboxyl
Autor:
Kathleen M. George, P. L. C. Small, Delphi Chatterjee, Patrick J. Brennan, Geewananda Gunawardana, and David Whittern
Publikováno v:
Journal of the American Chemical Society. 121:6092-6093
Publikováno v:
Carbohydrate research. 201(2)
Selective C-8 modifications of 2,6-anhydro-3-deoxy-D-glycero-D-talo-octonic acid ("2,3-dideoxy-beta-D-manno-2-octulosonic acid", 1a) were effected via the protected 8-hydroxy derivatives 2d and 2e. Swern oxidation of 2d and 2e gave the aldehydes 3a a
Publikováno v:
Journal of Organometallic Chemistry. 243:305-314
13C NMR chemical shift data are reported for a number of trivalent derivatives of P, As, Sb and Bi and their LNi(CO)3 complexes. Data for EMe3 and EPh3 (E = P, As, Sb and Bi), EEt3 and EBu3 (E = P, As and Sb) and PhEX2 and Ph2EX (E = P, As; X = Cl, M
Autor:
David Whittern, Nicholas C. Carpita
Publikováno v:
Carbohydrate Research. 146:129-140
A glucuronoarabinoxylan in which about six of every seven xylosyl residues were substituted with terminal arabinofuranosyl and glucosyluronic groups was extracted from developing maize coleoptiles with dilute alkali and purified by gel-permeation chr
Publikováno v:
Journal of Heterocyclic Chemistry. 20:1745-1747
The Friedel-Crafts reactions of optically active phenyloxirane with toluene and anisole were examined for stereospecificity. The enantiomeric ratios of the diarylethanol products were determined and compared to those of the same products obtained fro