Zobrazeno 1 - 10
of 18
pro vyhledávání: '"and Arlene E. McKeown"'
Autor:
Michel Journet, Zhihui Peng, Dalian Zhao, Arlene E. Mckeown, Guy R. Humphrey, Jeffrey T. Kuethe
Publikováno v:
Organic Process Research & Development. 20:227-232
A highly efficient, regioselective five-step synthesis of the TRPV1 antagonist 1 is described. The coupling of piperazine 7 with dichloropyrimidine 8 proceeded via a regioselective Pd-mediated amination affording product 11 in excellent yield. Conver
Autor:
Robert D. Wilson, George Zhou, Antony J. Davies, Gavin W. Stewart, Karel M. J. Brands, David Hands, Steven F. Oliver, Michael S. Ashwood, Robert A. Reamer, Ed Cleator, Matthew M. Bio, Ulf-H. Dolling, Khateeta M. Emerson, Faye J. Sheen, Arlene E. Mckeown, Andrew D. Gibb
Publikováno v:
Organic Process Research & Development. 13:543-547
A practical and efficient synthesis of 1,4,5,6-tetrahydro-3-(1H-tetrazol-5-yl)cyclopenta[c]pyrazole, 1, is described. A new one-pot process has been developed, starting from the commercially availa...
Autor:
Hinksmon J, Arlene E. Mckeown, McWilliams Jc, Michel Journet, Y.-K. Sun, Tillyer Rd, David M. Tellers, Guy R. Humphrey, Lisa DiMichele, Thorsten Rosner
Publikováno v:
Journal of the American Chemical Society. 128:17063-17073
Ruthenium complexes employing axially chiral ligands were found to be effective asymmetric hydrogenation catalysts for the reduction of alpha,beta-unsaturated ene acid 1-E to give 2, a prostaglandin D2 (PGD2) receptor antagonist. With [(S-BINAP)Ru(p-
Autor:
Richard D. Tillyer, Jean-François Marcoux, and Arlene E. McKeown, Dalian Zhao, Edward J. J. Grabowski, Michael C. Hillier
Publikováno v:
The Journal of Organic Chemistry. 70:8385-8394
A general asymmetric synthesis of substituted cycloalkyl[b]indoles has been accomplished. The key features of this approach are (1) the utilization of a Japp-Klingemann condensation/Fischer cyclization to prepare cycloalkyl[b]indolones, (2) the asymm
Publikováno v:
Journal of Organometallic Chemistry. 656:63-70
The zirconocene amide [Cp2Zr(Cl)N(CH2Ph)(2)] (5), and the zirconbcene ketimides [Cp2Zr(Cl)N=C(Bu')Ph] (7), and [Cp2Zr(Cl)N=C(NMe2)(2)] (9), have been prepared by the transmetallation reactions between the appropriate lithiated organonitrogen compound
Autor:
and Arlene E. McKeown, Charles Jenny, Alan R. Kennedy, David R. Armstrong, Robert E. Mulvey, Kenneth W. Henderson, Ian Little
Publikováno v:
Organometallics. 19:4369-4375
The metathetical reaction between the lithium 1-azaallyl compound [{HMPA·LiN(H)C(t-Bu)CH2}2] (1) with zirconocene dichloride (2) results in the formation of the zirconocene ketimide [Cp2Zr(Cl)N=C(t-Bu)CH3] (3; Cp = cyclopentadienyl) and lithium chlo
Autor:
Kenneth W. Henderson, Mark R. J. Elsegood, John F. Allan, Igor M. Rakov, Paul H. Moran, William Clegg, Arlene E. McKeown
Publikováno v:
Journal of Organometallic Chemistry. 602:15-23
Reaction of Me3Al with a series of aromatic ketones results in the precipitation of either dimethylaluminium enolates or alkoxides. In situ 1H-NMR spectroscopic studies of the reaction between Me3Al and acetophenone reveal a complex mixture of produc
Publikováno v:
Journal of the Chemical Society, Dalton Transactions. :4348-4353
Reaction of the phosphonates (RO)2P(O)CH2CN (R = Et I or PriII) with one molar equivalent of LiNPri2 in THF gave the metallated complexes [(RO)2P(O)CHCNLi·THF]∞ (R = Et 1 or Pri2). Crystallographic analyses of them reveal that they form dimeric Li
Autor:
Stephen T. Liddle, Fiona E. Keenan, William Clegg, Kenneth W. Henderson, Arlene E. McKeown, Robert E. Mulvey, Alan R. Kennedy
Publikováno v:
Journal of Organometallic Chemistry. 572:283-289
Reaction of the pre-formed crystalline amides [(PhCH2)2NLi] and [Me2AlN(CH2Ph)2] in the presence of pyridine results in the formation of the mixed metal complex [Me2Al{(PhCH2)2N}2Li·pyr] 1. Ab initio molecular orbital calculations indicate formation
Publikováno v:
Angewandte Chemie. 112:4037-4039