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pro vyhledávání: '"Houghton, Adrian"'
Autor:
Houghton, Adrian James.
Publikováno v:
Connect to e-thesis.
Thesis (Ph. D.)--University of Newcastle upon Tyne, 2009.
Externí odkaz:
http://hdl.handle.net/10443/790
Autor:
Houghton, Adrian James
Suppose that we wish to determine which models in a candidate set are most likely to have given rise to a set of observed data. Then, it is well-established that, from a Bayesian viewpoint, evaluation of the marginal likelihood for each candidate is
Externí odkaz:
http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.531779
Autor:
Houghton, Adrian M
Publikováno v:
BMJ: British Medical Journal, 2012 Jul . 345(7865), 29-29.
Externí odkaz:
https://www.jstor.org/stable/23279255
Autor:
Houghton, Adrian M
Publikováno v:
BMJ: British Medical Journal, 2012 Feb 01. 344(7842), 33-33.
Externí odkaz:
https://www.jstor.org/stable/41502021
Autor:
Houghton, Adrian Y.1, Hurmalainen, Juha2, Mansikkamäki, Akseli2, Piers, Warren E.1, Tuononen, Heikki M.2
Publikováno v:
Nature Chemistry. Nov2014, Vol. 6 Issue 11, p983-988. 6p.
Akademický článek
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Perfluorarylborane Lewis acids catalyse the addition of silicon–hydrogen bonds across C=C, C=N and C=O double bonds. This ‘metal-free’ hydrosilylation has been proposed to occur via borane activation of the silane Si–H bond, rather than throu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1222::e7ec31f39703e37141045a5f365a561d
http://urn.fi/URN:NBN:fi:jyu-201511253820
http://urn.fi/URN:NBN:fi:jyu-201511253820
The perfluorinated boraindene 3 was synthesized and fully characterized. Both computational and crystallographic data show that 3 is antiaromatic. Compound 3 was shown to react reversibly with H2 and to catalyse the hydrogenation of cyclohexene. The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1222::aed68121483cf657625aeab7da22b7ad
http://urn.fi/URN:NBN:fi:jyu-201511263836
http://urn.fi/URN:NBN:fi:jyu-201511263836
Akademický článek
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The perfluoro- and perprotiopentaphenylboroles 1 and 2 react with dihydrogen to effect H–H bond cleavage and formation of boracyclopentene products. The mechanism of this reaction has been studied experimentally through evaluation of the kinetic pr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=od______1222::4f40fdba0eadce97dc780ec29199808e
http://urn.fi/URN:NBN:fi:jyu-201511243796
http://urn.fi/URN:NBN:fi:jyu-201511243796