Zobrazeno 1 - 10
of 97
pro vyhledávání: '"Tomas Lebl"'
Autor:
José A. Fuentes, Mesfin E. Janka, Aidan P. McKay, David B. Cordes, Alexandra M. Z. Slawin, Tomas Lebl, Matthew L. Clarke
Publikováno v:
Molecules, Vol 29, Iss 4, p 845 (2024)
Phospholane-phosphites are known to show highly unusual selectivity towards branched aldehydes in the hydroformylation of terminal alkenes. This paper describes the synthesis of hitherto unknown unsaturated phospholene borane precursors and their con
Externí odkaz:
https://doaj.org/article/c7ed6d74183647efb7c6e89799f91194
Autor:
Brian A. Chalmers, David B. Cordes, Thomas Doig, Yuanyuan Du, Tomas Lebl, Meiyue Liu, Fraser Mealyou, Jasmine Rainer, Siobhan R. Smith, Ryan Walker, Iain A. Smellie
Publikováno v:
Molbank, Vol 2022, Iss 4, p M1524 (2022)
X-ray crystallography has been used to characterise the title compound for the first time, 1H NMR, 13C NMR and IR spectroscopic data has also been updated from earlier reports.
Externí odkaz:
https://doaj.org/article/aa0617f7cfab4349b9485c07fc5a6d4f
Autor:
Corrin Blake, Brian A. Chalmers, Lewis A. Clough, Dylan Clunie, David B. Cordes, Tomas Lebl, Timothy R. McDonald, Siobhan R. Smith, Elliott Stuart-Morrison, Iain A. Smellie
Publikováno v:
Molbank, Vol 2022, Iss 3, p M1435 (2022)
X-ray crystallography was used to characterise the title compound for the first time, and the 1H NMR, 13C NMR and IR spectroscopic data from earlier reports were also updated.
Externí odkaz:
https://doaj.org/article/396bdc5cb19f42d7ac1fd7e96797ba1a
Publikováno v:
Molecules, Vol 26, Iss 19, p 6039 (2021)
The bioactive natural product perophoramidine has proved a challenging synthetic target. An alternative route to its indolo[2,3-b]quinolone core structure involving a N-chlorosuccinimde-mediated intramolecular cyclization reaction is reported. Attemp
Externí odkaz:
https://doaj.org/article/f6adb2e6851541f08ee1e810fab333c3
Autor:
James R. D. Montgomery, Christopher S. Lancefield, Daniel M. Miles-Barrett, Katrin Ackermann, Bela E. Bode, Nicholas J. Westwood, Tomas Lebl
Publikováno v:
ACS Omega, Vol 2, Iss 11, Pp 8466-8474 (2017)
Externí odkaz:
https://doaj.org/article/d12a0511e55c492a9a9455573981df74
Autor:
Freideriki Michailidou, Tomas Lebl, Alexandra M. Z. Slawin, Sunil Vishnuprasadji Sharma, Murray J. B. Brown, Rebecca Jane Miriam Goss
Publikováno v:
Molecules, Vol 25, Iss 23, p 5513 (2020)
Fluorinated nucleoside analogues have attracted much attention as anticancer and antiviral agents and as probes for enzymatic function. However, the lack of direct synthetic methods, especially for 2′,3′-dideoxy-2′,3′-difluoro nucleosides, ha
Externí odkaz:
https://doaj.org/article/cdcccc80b6af495089b9188addd0cb9a
Publikováno v:
International Journal of Digital Curation, Vol 12, Iss 2 (2018)
Research funders have introduced requirements that expect researchers to properly manage and publicly share their research data, and expect institutions to put in place services to support researchers in meeting these requirements. So far the general
Externí odkaz:
https://doaj.org/article/78697ed9692a4e2a885cf2b6522844fe
Autor:
Nicholas J. Westwood, Sonia Lain, Tomas Lebl, Daumantas Matulis, Asta Zubrienė, Anna R. McCarthy, Louise L. Major, Vaida Morkūnaitė, Lisa Pirrie
Publikováno v:
Molecules, Vol 17, Iss 10, Pp 12206-12224 (2012)
The search for potent and selective sirtuin inhibitors continues as chemical tools of this type are of use in helping to assign the function of this interesting class of deacetylases. Here we describe SAR studies starting from the unselective sirtuin
Externí odkaz:
https://doaj.org/article/671838680b6349c49ea791e5f162cc7d
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 8, Iss 1, Pp 1271-1278 (2012)
Cyclododecane adopts a square-like structure with corner and edge CH2 groups. In this study erythro- and threo-1,2-difluorocyclododecanes were prepared to explore whether the two vicinal C–F bonds, with different relative configurations, preferably
Externí odkaz:
https://doaj.org/article/7d8cddb0e9e24828aa7378c217b1e7fb
Autor:
Alexandra M. Z. Slawin, Tomas Lebl, David B. Cordes, Cameron L. Carpenter-Warren, Neil S. Keddie, Rodrigo P. F. De A. Gouy, Brian A. Chalmers, Iain A. Smellie, Iain L. J. Patterson
Publikováno v:
Journal of Chemical Education. 98:3608-3613
This work presents a simple protocol that demonstrates the use of an inexpensive household carbon monoxide detector as a useful tool to detect the release of carbon monoxide gas from thermal cheletropic decarbonylation reactions. The carbon monoxide
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::59d4d5cb4b8ad959cfb39861e5a72bdf
https://doi.org/10.1021/acs.jchemed.1c00517
https://doi.org/10.1021/acs.jchemed.1c00517