Zobrazeno 1 - 9
of 9
pro vyhledávání: '"George Robert Hodges"'
Autor:
Vijayagopal Gopalsamuthiram, Krishna Sawant, Srinivas Subramanian, Nigel James Willetts, George Robert Hodges, Matthew Brian Hotson, Sujit K. Ghorai, Anne-Marie Hogan, James Nicholas Scutt, Louisa Whalley, Dinesh Pagar, Tomas Smejkal, Jonathan Dallimore, Anup M. Jawalekar
Publikováno v:
Organic Process Research & Development. 21:1625-1632
Aryl-1,3-diones represent a promising new class of herbicidal acetyl-CoA carboxylase (ACCase) inhibitors. The original synthesis of this structural motif employed in the research phase involved a selenium oxide mediated oxidation, the use of diazoace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::612135aa6a91bc9dae451b94ce374133
https://doi.org/10.1021/acs.oprd.7b00241
https://doi.org/10.1021/acs.oprd.7b00241
Publikováno v:
Dale, H J A, Hodges, G & Lloyd-jones, G C 2019, ' Taming Ambident Triazole Anions: Regioselective Ion-Pairing Catalyzes Direct N-Alkylation with Atypical Regioselectivity ', Journal of the American Chemical Society . https://doi.org/10.1021/jacs.9b02786
Controlling the regioselectivity of ambident nucleophiles towards alkylating agents is a fundamental problem in heterocyclic chemistry. Unsubstituted triazoles are particularly challenging, often requiring inefficient stepwise protection-deprotection
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::be17898ddcba22d85b034e3c47372d90
https://hdl.handle.net/20.500.11820/d44d7680-ad0d-4bad-8cda-4f657c48d38f
https://hdl.handle.net/20.500.11820/d44d7680-ad0d-4bad-8cda-4f657c48d38f
Publikováno v:
European Journal of Organic Chemistry. 2016:2821-2827
The kinetics of the addition of phenol to diisopropylcarbodiimide, and reaction of the resulting N,N′-diisopropyl-O-phenylisourea with hydroxide, are reported. The isourea is generated by a slow overall termolecular equilibrium process, inhibited b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c73f114b8ccceb3a46e1f13a7950d594
https://doi.org/10.1002/ejoc.201600386
https://doi.org/10.1002/ejoc.201600386
Autor:
Mark R. Wilson, David Anthony Jackson, Andrew Whiting, Hayley Charville, George Robert Hodges
Publikováno v:
European Journal of Organic Chemistry. 2011:5981-5990
Calorimetric studies of the mixing of a series of carboxylic acids and amines have been carried out to measure heat output, which has been compared with their ability to react to form carboxylate ammonium salts and amides. In order to identify which
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2b82791144fa724bf934eceb1940cdf3
https://doi.org/10.1002/ejoc.201100714
https://doi.org/10.1002/ejoc.201100714
Autor:
Andrew Charles Shaw, John P. O'Connell, George Robert Hodges, Chiara Piccolo, Patrick M. Piccione, Rafiqul Gani
A generic modelling framework for phase transition catalyst based reacting systems has been developed and converted into a software tool. The modelling framework accommodates models of different types representing different sub-systems of the PTC-bas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e482d22bf46b489526762919835eaffc
https://doi.org/10.1016/b978-0-444-59520-1.50010-5
https://doi.org/10.1016/b978-0-444-59520-1.50010-5
Issues related to the design of biphasic (liquid) catalytic reaction operations are discussed. A chemical system involving the reaction of an organic-phase soluble reactant (A) with an aqueous-phase soluble reactant (B) in the presence of phase trans
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f209d0b8cd2e4ace653af8907f7d689a
https://doi.org/10.1016/b978-0-444-53711-9.50054-7
https://doi.org/10.1016/b978-0-444-53711-9.50054-7
Publikováno v:
Chemical communications (Cambridge, England). 46(11)
Despite the amide formation reaction being one of the key cornerstone reactions in organic chemistry, the direct amide formation is both little used and little explored. Acceptance of the feasibility and general applicability of the reaction depends
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c3ec3fc87b22f6460790cc508b135db
https://pubmed.ncbi.nlm.nih.gov/20198220
https://pubmed.ncbi.nlm.nih.gov/20198220
Publikováno v:
ChemInform. 41
Employing co-catalytic zinc reagents facilitates the iron-catalysed Suzuki cross-coupling of tetraarylborates with both benzyl and 2-heteroaryl halides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b60b293b72d652490eeedfff1c1ef29b
https://doi.org/10.1002/chin.201011046
https://doi.org/10.1002/chin.201011046
Publikováno v:
Chemical communications (Cambridge, England). (42)
Employing co-catalytic zinc reagents facilitates the iron-catalysed Suzuki cross-coupling of tetraarylborates with both benzyl and 2-heteroaryl halides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4415f8b6621297ad0b9ca93410434b7c
https://pubmed.ncbi.nlm.nih.gov/19841799
https://pubmed.ncbi.nlm.nih.gov/19841799