Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Francis Orerenyo Ginah"'
Cooperative Catalyst Effects in Palladium-Mediated Cyanation Reactions of Aryl Halides and Triflates
Autor:
Edward C. Bell, Lisa M. Pagh, Anderson Benjamin Alan, James P. Wepsiec, Francis Orerenyo Ginah, Nancy Kay Harn
Publikováno v:
The Journal of Organic Chemistry. 63:8224-8228
Substoichiometric quantities of copper or zinc species dramatically improve both conversion rate and efficiency of Pd(0)-catalyzed cyanation reactions. The optimum reaction conditions involve the use of a nitrile solvent, NaCN, and a catalyst system
Publikováno v:
The Journal of Organic Chemistry. 63:5050-5058
A general regio- and stereoselective synthesis of 3,3-diarylacrylamides is reported. Palladium-catalyzed coupling reactions of propiolamides with aryl halides provide arylpropiolamides. A subsequent hydroarylation reaction of these arylpropiolamides
Publikováno v:
Synthetic Communications. 26:3491-3494
A robust process for the preparation of multikilogram quantities of 2-chloro-4,6-dimethoxy-1,3,5-triazine (1) is described.
Autor:
J. Jeffry Howbert, Karen Lynn Lobb, Francis Orerenyo Ginah, Hansen Guy Joe, Stuart L. Fort, Jason S. Cronin, Cho Sung-Yong Stephen, Philip Arthur Hipskind, Huff Bret Eugene
Publikováno v:
The Journal of Organic Chemistry. 60:7033-7036
Publikováno v:
ChemInform. 27
A robust process for the preparation of multikilogram quantities of 2-chloro-4,6-dimethoxy-1,3,5-triazine (1) is described.
Publikováno v:
ChemInform. 29
A general regio- and stereoselective synthesis of 3,3-diarylacrylamides is reported. Palladium-catalyzed coupling reactions of propiolamides with aryl halides provide arylpropiolamides. A subsequent hydroarylation reaction of these arylpropiolamides
Autor:
Nancy Kay Harn, Lisa M. Pagh, Francis Orerenyo Ginah, James P. Wepsiec, Anderson Benjamin Alan, Edward C. Bell
Publikováno v:
ChemInform. 30
Substoichiometric quantities of copper or zinc species dramatically improve both conversion rate and efficiency of Pd(0)-catalyzed cyanation reactions. The optimum reaction conditions involve the use of a nitrile solvent, NaCN, and a catalyst system
Autor:
James Densmore Copp, Douglas Patton Kjell, Stephen C. Stirm, Francis Orerenyo Ginah, and Marvin M. Hansen, Slattery Brian James
Publikováno v:
Organic Process Research & Development. 4:295-297
The development of a manufacturable synthesis of LY213829 (4-thiazolidinone-5-[3,5-bis(1,1-dimethylethyl)-4-hydroxyphenyl] methyl) is described. Rather than reduction to eliminate the thiocarbonyl from the rhodanine moiety, the new route utilizes a n
Autor:
Greg W. Ebert, Deborah R. Pfennig, Thomas A. Donovan, Francis Orerenyo Ginah, Scott D. Suchan
Publikováno v:
The Journal of Organic Chemistry. 55:584-589
La copulation chimique d'alcanes halogenes et la cyclisation d'α,ω-dihalogeno alcanes catalysees par une forme activee du cuivre zerovalent ont ete etudiees
Autor:
Greg W. Ebert, T. A. Jun. Donovan, Francis Orerenyo Ginah, Scott D. Suchan, Deborah R. Pfennig
Publikováno v:
ChemInform. 21
The homocoupling reaction of allyl or benzyl halides (I) is catalyzed by an activated Cu(0) complex, yielding the dimers (II), and in the case of benzyl chloride (Ib), the reduced monomer (IIIb).