Zobrazeno 1 - 10
of 34
pro vyhledávání: '"Justin R. Denton"'
Publikováno v:
Analytical Methods. 8:4659-4663
2-Chloromalonaldehyde (2-ClMA) is utilized in the pharmaceutical sector as a reagent to form thiazole heterocycles which can be further functionalized. This present work describes a hydrophilic interaction chromatography (HILIC) strategy for the trac
Publikováno v:
Journal of Chromatography & Separation Techniques.
Control of regioisomer impurities within pharmaceutical raw materials, intermediates, and active pharmaceutical ingredients are of major concern for the pharmaceutical industry. If regioisomer impurities are possible, their detection and quantitation
Publikováno v:
Anal. Methods. 6:6565-6570
The utilization of L-valine for its chiral centre is increasing in the fine chemical, biologic, and pharmaceutical sectors. Therefore, a simple and reliable chirality procedure is needed to assure that trace levels of D-valine are not present. The pr
Publikováno v:
Organic Letters. 13:4316-4319
A triple cascade process was developed for the rapid synthesis of polycyclic benzo-fused dihydrofurans. The first step is a rhodium-catalyzed cyclopropanation of α-aryldiazoketones with alkenes. This is followed by a silver-catalyzed ring expansion
Autor:
Justin R. Denton
Publikováno v:
Synthetic Communications. 41:770-776
A protocol has been developed to purify 9-(trifluoroacetyl)anthracene from anthracene, the major impurity associated in its synthesis. The protocol utilizes a chemoselective thermal Diels–Alder reaction, employing maleic anhydride as the dienophile
Autor:
Justin R. Denton
Publikováno v:
Synthesis. 2010:775-782
Sulfonamide heterocycles, specifically 3-acylindoles, undergo a deprotection/alkylation sequence in the presence of an appropriate alcohol when cesium carbonate or potassium carbonate and a phase-transfer catalyst are utilized. The outcome of the one
Publikováno v:
Synthesis. 2009:2840-2846
The synthesis of a silyl-protected derivative of 3-hydroxyvibsanin E has been achieved. The key step is a regio-and stereoselective C-H hydroxylation of an advanced tricyclic intermediate by means of a Rubottom oxidation.
Autor:
Huw M. L. Davies, Justin R. Denton
Publikováno v:
Organic Letters. 11:787-790
The reaction of a variety of alpha-aryl-alpha-diazo ketones with activated olefins, catalyzed by the adamantyl glycine-derived dirhodium complex Rh(2)(S-PTAD)(4), generates cyclopropyl ketones with high diastereoselectivity (up to95:5 dr) and enantio
Publikováno v:
Journal of pharmaceutical and biomedical analysis. 115
2-Hydroxypyridine-1-oxide (HOPO) is utilized in the pharmaceutical sector to facilitate the formation of amide bonds. This present work describes the development of a HPLC high pH ion-pairing method for the trace analysis of HOPO in pharmaceutically
Publikováno v:
ChemInform. 42
The two-step sequence allows the access to a broad spectrum of multisubstituted benzofuran skeletons.