Zobrazeno 1 - 10
of 32
pro vyhledávání: '"Andrew J. McCarroll"'
Publikováno v:
ARKIVOC, Vol 2007, Iss 11, Pp 172-182 (2007)
Externí odkaz:
https://doaj.org/article/97102a69e51b4d3aadac6cd52a02dcde
Autor:
Andrew J. McCarroll, John C. Walton
Publikováno v:
ARKIVOC, Vol 2002, Iss 3, Pp 55-62 (2002)
Externí odkaz:
https://doaj.org/article/6c0bdc2f08934d52be7d18d6f47ba2b4
Autor:
Gary Nelson, Henry Forward, David McGarry, Jonathan Cheung, Andrew J. Ratcliffe, James Kirkham, Mark Craighead, Cedric Charrier, Zoe Gault, Ian R. Cooper, Catherine E. Warrilow, John Maclean, Emmanuel Moyo, Neil R. Stokes, Andrew J. McCarroll, Anne-Marie Salisbury, Victoria J. Savage, Mark Pichowicz, Stuart A. Best, Diarmaid Hughes, Rolf Peter Walker, Richard Metzger, Sha Cao
Publikováno v:
Bioorganicmedicinal chemistry letters. 26(17)
There is an urgent and unmet medical need for new antibacterial drugs that tackle infections caused by multidrug-resistant (MDR) pathogens. During the course of our wider efforts to discover and exploit novel mechanism of action antibacterials, we ha
Autor:
Paul G. Wyatt, Alan H. Fairlamb, Iain T. Collie, Andrew J. McCarroll, Julie A. Frearson, Malcolm F. G. Stevens, Irene Hallyburton, Amy S. Capes, Stephen Patterson, Susan Wyllie, Ian H. Gilbert
Publikováno v:
Bioorganic & Medicinal Chemistry
Graphical abstract
Quinols have been developed as a class of potential anti-cancer compounds. They are thought to act as double Michael acceptors, forming two covalent bonds to their target protein(s). Quinols have also been shown to have activi
Quinols have been developed as a class of potential anti-cancer compounds. They are thought to act as double Michael acceptors, forming two covalent bonds to their target protein(s). Quinols have also been shown to have activi
Autor:
Charles S. Matthews, Andrew D. Westwell, Tracey D. Bradshaw, Malcolm F. G. Stevens, Andrew J. McCarroll
Publikováno v:
Journal of Medicinal Chemistry. 50:1707-1710
Interaction of 2-iodoaniline or 5-fluoro-2-iodoaniline with a range of arylsulfonyl chlorides affords sulfonamides that undergo Sonogashira couplings under thermal or microwave conditions with the alkyne 4-ethynyl-4-hydroxycyclohexa-2,5-dien-1-one fo
Publikováno v:
Tetrahedron. 59:4275-4280
Several 2- and 4-alkylcyclohexadienones were prepared and shown to accept electrons to produce ketyl radical anions that dissociated rapidly at room temperature to release carbon-centered radicals and an aromatic phenoxide type anion. In the PET proc
Autor:
John C. Walton, Andrew J. McCarroll
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :3215-3229
Autor:
Andrew J. McCarroll, John C. Walton
Publikováno v:
Angewandte Chemie International Edition. 40:2224-2248
Cascade, domino, or tandem processes, that link together two or more transformations in one pot, are increasing in popularity because they lead to improvements in synthetic efficiency and decreases in environmental impact. Not only do these cascades
Autor:
Andrew J. McCarroll, John C. Walton
Publikováno v:
Angewandte Chemie. 113:2282-2307
Kaskaden-, Domino- und Tandemreaktionen, bei denen zwei oder mehr chemische Umwandlungen als Eintopfreaktionen ablaufen, werden immer popularer, da sie die Effizienz von Synthesen verbessern und die Umwelt weniger belasten. Diese Kaskaden enthalten n
Publikováno v:
Journal of the American Chemical Society. 122:5455-5463
Radicals containing α-boronate substituents were generated by bromine abstraction from 1-bromoalkyldioxaborolanes (boronic esters), by addition to vinyl boronate, and by hydrogen abstraction from alkyldioxaborolanes and observed by EPR spectroscopy.