Zobrazeno 1 - 10
of 19
pro vyhledávání: '"Magnus W. P. Bebbington"'
Publikováno v:
Molecules, Vol 19, Iss 10, Pp 15535-15545 (2014)
Detailed analysis of calculated data from an experimental/computational study of intramolecular furan Diels–Alder reactions has led to the unusual discovery that the mean contraction of the newly forming C-C σ-bonds from the transition state to th
Externí odkaz:
https://doaj.org/article/ca55ecb008e84061a9813413b92ec89e
Autor:
Angela Fong, Cameron L. Campbell, Silvia Huynh, Laura J. McCormick McPherson, Simon J. Teat, Magnus W. P. Bebbington, Scott J. Dalgarno
Publikováno v:
Chemical Communications. 58:3302-3305
Ring-opening of furans at the equatorial methylene bridge positions of a calix[4]arene gives access to a range of new molecules (in good yield) that have widespread potential impact in supramolecular chemistry amongst other areas.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a34e6cd7d5e45ba70520f67e6370d09d
https://doi.org/10.1039/d1cc06889j
https://doi.org/10.1039/d1cc06889j
Autor:
James O. F. Thompson, Magnus W. P. Bebbington, Jason B. Greenwood, Thomas Y. Cowie, Stuart W. Crane, O. Ghafur, Anita G. Lindsay, Dave Townsend
Publikováno v:
Crane, S W, Ghafur, O, Cowie, T Y, Lindsay, A G, Thompson, J O F, Greenwood, J B, Bebbington, M W P & Townsend, D 2019, ' Dynamics of electronically excited states in the eumelanin building block 5,6-dihydroxyindole ', Physical Chemistry Chemical Physics, vol. 21, no. 15, pp. 8152-8160 . https://doi.org/10.1039/c9cp00620f
We report the first excited state dynamics study of gas-phase 5,6-dihydroxyindole (5,6-DHI), a key building block of eumelanin pigments that are found throughout nature and serve as important photo-protective compounds. Time-resolved ion-yield measur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6facdf59ed9741d6bd429b1d8e441154
https://doi.org/10.1039/c9cp00620f
https://doi.org/10.1039/c9cp00620f
Autor:
Robert L. Rae, Magnus W. P. Bebbington, Andrew W. Prentice, Martin J. Paterson, Mathilde Rougé, Marcos Veguillas, Thomas Y. Cowie, Justyna M. Żurek
Publikováno v:
The Journal of Organic Chemistry. 82:6656-6670
Nitrofurans undergo intramolecular Diels-Alder reactions with tethered electron-poor dienophiles more rapidly and in higher yield than non-nitrated furans. Computational studies indicate that increased stabilization of a partial positive charge on th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7375c4e723bae6c599c5004c3ac323d
https://doi.org/10.1021/acs.joc.7b00781
https://doi.org/10.1021/acs.joc.7b00781
Autor:
Magnus W. P. Bebbington
Publikováno v:
Chemical Society Reviews. 46:5059-5109
For the first time a general overview of approaches to the synthesis of natural product analogues is presented. This reflects a process of evolution of natural product synthesis which has accelerated in the years since the implementation of diversity
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18567f741d20724d44410cca529cdc7c
https://doi.org/10.1039/c6cs00842a
https://doi.org/10.1039/c6cs00842a
Autor:
Magnus W. P. Bebbington, Thomas Y. Cowie, Justyna M. Żurek, Lorna Kennedy, Martin J. Paterson
Publikováno v:
European Journal of Organic Chemistry. 2015:3818-3823
Crossed McMurry reactions of bifuran- or bithiophenedicarbaldehydes with bipyrroledicarbaldehydes have been studied for the first time. Only those porphycenic macrocycles derived from homocoupled McMurry products were formed. The results are explaine
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c259ec7cba0014ffc786af652b80bbef
https://doi.org/10.1002/ejoc.201500221
https://doi.org/10.1002/ejoc.201500221
Publikováno v:
Molecules, Vol 19, Iss 10, Pp 15535-15545 (2014)
Molecules
Volume 19
Issue 10
Pages 15535-15545
Molecules
Volume 19
Issue 10
Pages 15535-15545
Detailed analysis of calculated data from an experimental/computational study of intramolecular furan Diels-Alder reactions has led to the unusual discovery that the mean contraction of the newly forming C-C σ-bonds from the transition state to the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ea37742d29981c2a509d5ca9b9b9af79
http://www.mdpi.com/1420-3049/19/10/15535
http://www.mdpi.com/1420-3049/19/10/15535
Addition of thiols to 7-azabicyclo[2.2.1]heptadienes such as 16 leads exclusively to 7-thio-substituted 2-azabicyclo[2.2.1]-hept-5-enes 17 in good yields via tandem intermolecular radical addition—homoallylic radical rearrangement.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::461688173e37c315a2d2c727b47efc62
https://ora.ox.ac.uk/objects/uuid:e0a53f64-b716-48d2-a99d-10bb693e5d51
https://ora.ox.ac.uk/objects/uuid:e0a53f64-b716-48d2-a99d-10bb693e5d51
Autor:
Paul A. J. Bagot, Magnus W. P. Bebbington, Manfred Buck, Kenneth G. McKendrick, Carla Waring, Matthew L. Costen, Minna T. Räisänen
The depth of penetration of photolytically generated, gas-phase O( 3P) atoms into thioalkyl self-assembled monolayers (SAMs) has been investigated. Custom-synthesized, site-selectively deuterated SAMs were prepared on Au substrates and characterized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2de2134e0940641220fcc99d3b7d202a
https://ora.ox.ac.uk/objects/uuid:c51889fb-2b5c-445f-bcab-0c5dc813e00d
https://ora.ox.ac.uk/objects/uuid:c51889fb-2b5c-445f-bcab-0c5dc813e00d
Autor:
Mari C. M. Higginbotham, Anita G. Lindsay, Lorna Kennedy, Andreas Troester, Magnus W. P. Bebbington
Publikováno v:
ChemInform. 46
The first gold-catalyzed preparation of cyclic sulfamidates, leading to a range of unusually substituted and sterically hindered products under mild conditions is reported.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4653d7e6443881304871becd8a75dd6c
https://doi.org/10.1002/chin.201520214
https://doi.org/10.1002/chin.201520214