Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Timothy M. Gregg"'
Publikováno v:
Journal of Chemical Education. 98:1732-1735
Aldol chemistry is highlighted in many introductory organic chemistry laboratory experiments because it provides synthesis, mechanism, and experimental challenges for students. In the experiment described here, students synthesize dibenzalacetone der
Publikováno v:
Biophysical Journal. 104(3):565-574
Agonists, including the neurotransmitter acetylcholine (ACh), bind at two sites in the neuromuscular ACh receptor channel (AChR) to promote a reversible, global change in protein conformation that regulates the flow of ions across the muscle cell mem
Publikováno v:
Proceedings of the National Academy of Sciences. 108:4328-4333
Allosteric proteins use energy derived from ligand binding to promote a global change in conformation. The “gating” equilibrium constant of acetylcholine receptor-channels (AChRs) is influenced by ligands, mutations, and membrane voltage. We engi
Publikováno v:
Tetrahedron Letters. 51:6429-6432
Rates of cyclopropanation for mono- and disubstituted allenes have been measured relative to standard substrates in reaction with aryldiazoacetate esters catalyzed by Rh2(S-DOSP)4. Phenylallene derivatives exhibited a linear correlation of rate with
Publikováno v:
Journal of the American Chemical Society. 125:15902-15911
The mechanism of the dirhodium tetracarboxylate catalyzed cyclopropanation of alkenes with both unsubstituted diazoacetates and vinyl- and phenyldiazoacetates was studied by a combination of (13)C kinetic isotope effects and density functional theory
Publikováno v:
Psychopharmacology. 167:386-392
"Agonist" therapy for drug addiction proposes that a long acting analog, with similar properties to the abused substance might serve as a useful therapeutic agent. HD-23 is a very long acting tropane analog that displays a neurochemical profile simil
Publikováno v:
Organic Letters. 11:4434-4436
Reaction of monosubstituted allenes with aryldiazoacetate esters under dirhodium tetracarboxylate catalysis led to alkylidene cyclopropane products in 80-90% ee. Monosubstituted alkyl- and arylallene substrates gave 60-75% yield under standard condit
Publikováno v:
The Journal of Organic Chemistry. 62:3715-3721
Autor:
Jeremy P. Olson, Changming Qin, Huw M. L. Davies, Kathryn M. Chepiga, Timothy M. Gregg, Joshua S. Alford, Spandan Chennamadhavuni
Publikováno v:
Tetrahedron. 69(27-28)
Catalytic enantioselective methods for the generation of cyclopropanes have been of long standing pharmaceutical interest. Chiral dirhodium(II) catalysts prove to be an effective means for the generation of diverse cyclopropane libraries. Rh2(R-DOSP)
Publikováno v:
Journal of the American Chemical Society. 135(45)
Reaction kinetics and mechanistic studies for ethylene-internal alkyne metathesis promoted by the phosphine-free initiator Ru1 (Piers's catalyst) is described. The kinetic order of reactants and catalyst was determined. The effect of ethylene was stu