Zobrazeno 1 - 10
of 19
pro vyhledávání: '"D. David Hennings"'
Autor:
Sean Broce, Florian Ermini, Leslie J. Holsinger, Stephen S. Dominy, Michael J. Detke, Leo Rodriguez, Ursula Haditsch, Casey C. Lynch, D. David Hennings, Mai Nguyen, Jianhong Wang, Shirin Arastu-Kapur, Debasish Raha
Publikováno v:
SSRN Electronic Journal.
Gingipains are protease virulence factors from the periodontal bacterial pathogen Porphyromonas gingivalis and were recently identified in greater than 90% of Alzheimer’s disease (AD) brains. Studies in wild-type mice and rats have demonstrated tha
Publikováno v:
Organic Letters. 12:5526-5529
A series of 2-phenylaminothiazolines have been prepared from the corresponding N-(2-hydroxyethyl)-N'-phenylthioureas under mild reaction conditions using either thio-CDI (1,1'-thiocarbonyldiimidazole) or CDI (1,1'-carbonyldiimidazole) to promote the
Publikováno v:
Tetrahedron Letters. 51:3709-3711
A practical method for the preparation of single component biaryl-urea analogs of capreomycin is described. The protocol involves derivatization of capreomycin followed by global protection of the capreomycin analog mixture. The individual components
Autor:
D. David Hennings, Robert M. Williams
Publikováno v:
Synthesis. 2000:1310-1314
Publikováno v:
Synthesis. 2000:399-402
Publikováno v:
Organic Letters. 1:1205-1208
A convenient new procedure is described for both inter- and intramolecular homocoupling of aryl halides (Ullmann reaction) using catalytic palladium in the presence of hydroquinone, a homogeneous reductant. Optimal conditions for the reductive coupli
Publikováno v:
Tetrahedron Letters. 38:6379-6382
Substituted benzo-fused heterocycles such as indoles, benzofurans, and a benzopyran were obtained using an intramolecular cross-coupling of vinyl halides with phenols. This transformation represents a new route to these heterocycles and is accomplish
ChemInform Abstract: A Selective and Convenient Method for the Synthesis of 2-Phenylaminothiazolines
Publikováno v:
ChemInform. 42
Thioureas which are substituted α to the amine of the amino alcohol are converted to thiazoline products when treated with CDI.
Publikováno v:
ChemInform. 28