Zobrazeno 1 - 10
of 25
pro vyhledávání: '"Timothy J. C. O'Riordan"'
Autor:
Daniel Graham Stark, Lucas Bacheley, Shuyue Zhang, Claire M. Young, Timothy J. C. O'Riordan, Andrew D. Smith, Alexandra M. Z. Slawin
Funding: ERC under the European Union's Seventh Framework Programme (FP7/2007–2013) / ERC grant agreement no 279850. We thank Syngenta and EPSRC grant No. EP/K503162/1 (DGS), ADS thanks the Royal Society for a Wolfson Research Merit Award. A protoc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::43e42ff15f3c2639618ec6bd6a42a8d5
https://hdl.handle.net/10023/20754
https://hdl.handle.net/10023/20754
Autor:
Timothy J. C. O'Riordan
Publikováno v:
Current Opinion in Green and Sustainable Chemistry. 13:158-163
Producing enough food of sufficient quality to feed an ever increasing population faces many challenges. This will require higher yields from agricultural production to meet the demands of changing population demographics using the limited natural re
Publikováno v:
Synthesis. 49:3303-3310
This short review highlights select examples of enantioselective Lewis base promoted reactions that use tertiary amine (cinchona alkaloids, isothioureas, and DMAP/PPY derivatives) or NHC catalysts and employ aryloxide-promoted catalyst turnover from
Autor:
Bridget V. Hogg, Barry Elsdon, Daniel P. Kloer, Timothy Robert Hawkes, Phillip J. Milnes, Shanaaz Tayab, Saranga Ranasinghe, Karine Lecoq, Matthew M. W. McLachlan, Richard Dale, John Martin Clough, Stephen E. Shanahan, Timothy J. C. O'Riordan, Karen D. Sumner, Anushka Howell
Publikováno v:
Pest Management Science. 72:2254-2272
BACKGROUND Exploiting novel herbicidal modes of action is an important method to overcome the challenges faced by increasing resistance and regulatory pressure on existing commercial herbicides. Recent reports of inhibitors of enzymes in the non-meva
Autor:
Stuart MacGregor, Patrick Williamson, Andrew D. Smith, Emma R Gayner, Alexandra M. Z. Slawin, Daniel Graham Stark, James E. Taylor, Ryan W. F. Kerr, Timothy J. C. O'Riordan, Stefania Francesca Musolino
We thank Syngenta and the EPSRC (grant code EP/K503162/1) (DGS), and the EPSRC Centre for Doctoral Training in Critical Resource Catalysis (CRITICAT, grant code EP/L016419/1) (ERG,SFM, RWFK) for funding. The European Research Council under the Europe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::df035296f38d0ff426a0ccf29934a999
https://hdl.handle.net/10023/9335
https://hdl.handle.net/10023/9335
Autor:
Alexandra M. Z. Slawin, Daniel Graham Stark, Andrew D. Smith, Timothy J. C. O'Riordan, Claire M. Young
Publikováno v:
Organicbiomolecular chemistry. 14(34)
The authors thank Syngenta and the EPSRC (grant code EP/K503162/1) (DGS) for funding. The European Research Council under the European Union’s Seventh Framework Programme (FP7/2007-2013) ERC Grant Agreement No. 279850 is also acknowledged (CMY). AD
(Chemical Equation Presented) In, out, olefin about: A ruthenium hydride complex derived from the Grubbs second-generation metathesis catalyst has proven to be an efficient catalyst for the selective isomerization of terminal olefins to the correspon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac715b2db1d62585dec844e88e717936
https://doi.org/10.1002/anie.200804617
https://doi.org/10.1002/anie.200804617
This paper reports the synthesis of the alkaloid natural product (±)-cylindricine C, in addition to a formal synthesis of (±)-cylindricine A. The key step in our sequence is the (ipso) regioselective addition of an alkyl Grignard reagent to a C-2 s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::65ebcdaf56f16b2cc439c55494318733
https://doi.org/10.1016/j.tet.2010.05.044
https://doi.org/10.1016/j.tet.2010.05.044
Autor:
Louis C. Morrill, Andrew D. Smith, Alexandra M. Z. Slawin, David B. Cordes, Timothy J. C. O'Riordan, Daniel Graham Stark
Publikováno v:
ChemInform. 47
The title compounds are synthesized from N-tosyliminoacrylates and aroylacrylates by a Michael addition-lactamization/lactonization cascade reaction.
Autor:
Christopher R. Jones, Manuel Peifer, Timothy J. C. O'Riordan, Timothy J. Donohoe, Timothy J. Miles
Publikováno v:
Organic Letters. 14:5460-5463
The asymmetric synthesis of the key pyrrolidinone core, including a highly elaborated exocyclic carbon chain, of the γ-lactam β-lactone antibiotic oxazolomycin A is described. Principal features include the Birch reduction of an aromatic pyrrole nu