Zobrazeno 1 - 6
of 6
pro vyhledávání: '"Jonathan W. Hall"'
Autor:
Michael K. Whittlesey, Damien Bouchet, Catherine S. J. Cazin, Mary F. Mahon, Jonathan W. Hall
Publikováno v:
Hall, J W, Bouchet, D, Mahon, M F, Whittlesey, M K & Cazin, C S J 2021, ' Synthetic Access to Ring-Expanded N-Heterocyclic Carbene (RE-NHC) Copper Complexes and their Performance in Click Chemistry ', Organometallics, vol. 40, no. 9, pp. 1252-1261 . https://doi.org/10.1021/acs.organomet.1c00039
The facile syntheses of ring-expanded N-heterocyclic carbene (RE-NHC) copper(I) halide complexes are reported. The method makes use of a weak inorganic base in a green solvent. The reaction times can be greatly reduced by use of this weak-base route
Autor:
David J. Liptrot, Mary F. Mahon, Jonathan W. Hall, John P. Lowe, Rex S. C. Charman, Thomas M. Horsley Downie
Publikováno v:
Dalton Transactions. 50:16336-16342
Reaction of bis(pinacolato)diboron with (6-Dipp)CuOtBu generates a ring-expanded N-heterocyclic carbene supported copper(I) boryl, (6-Dipp)CuBpin. This compound showed remarkable stability and was characterised by NMR spectroscopy and X-ray crystallo
Autor:
Jonathan W. Hall, Michael K. Whittlesey, Mary F. Mahon, Thomas P. Collier Finn, Claire L. McMullin, John P. Lowe, David J. Liptrot, Thomas M. Horsley Downie
Publikováno v:
Chemical Communications. 56:13359-13362
A range of N-heterocyclic carbene-supported copper diphenylphosphides (NHC = IPr, 6-Dipp, SIMes and 6-Mes) were synthesised. These include the first reports of ring-expanded NHC–copper(I) phosphides. The compounds were characterised by NMR spectros
Publikováno v:
Hall, J, Seeberger, F, Mahon, M & Whittlesey, M 2020, ' (carbene)CuF Complexes Featuring Bulky Arduengo-Type, Ring-Expanded, and Cyclic (Alkyl)(amino)carbenes : Applications in Catalytic Aldehyde Allylation ', Organometallics, vol. 39, no. 1, pp. 227-233 . https://doi.org/10.1021/acs.organomet.9b00772
Five examples of two-coordinate copper(I) fluoride complexes stabilized by five-, six-, and seven-membered-ring N-heterocyclic carbenes or a cyclic (alkyl)(amino)carbene have been prepared, structurally characterized, and employed in the catalytic al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9743dc2c9244b66206165ee797b73ab5
https://purehost.bath.ac.uk/ws/files/202290785/Whittlesey_FINAL_revised_MS_v1.pdf
https://purehost.bath.ac.uk/ws/files/202290785/Whittlesey_FINAL_revised_MS_v1.pdf
Autor:
Jonathan W. Hall, Paul Brunel, Mateusz K. Cybulski, Lee R. Collins, Michael K. Whittlesey, Mary F. Mahon, Darcy M. L. Unson
Publikováno v:
Hall, J, Unson, D, Brunel, P, Collins, L, Cybulski, M, Mahon, M & Whittlesey, M 2018, ' Copper-NHC-Mediated Semi-Hydrogenation and Hydroboration of Alkynes: Enhanced Catalytic Activity Using Ring-Expanded Carbenes ', Organometallics, vol. 37, no. 18, pp. 3102-3110 . https://doi.org/10.1021/acs.organomet.8b00467
A series of two-coordinate copper tert-butoxide complexes bearing five-, six-, and seven-membered ring N-heterocyclic carbenes, prepared by protonolysis of (NHC)CuMes with tBuOH, have been used as catalytic precursors in the semihydrogenation of alky
Autor:
Alexander R. Nödling, Katarzyna Świderek, Raquel Castillo, Jonathan W. Hall, Antonio Angelastro, Louis C. Morrill, Yi Jin, Yu-Hsuan Tsai, Vicent Moliner, Louis Y. P. Luk
Publikováno v:
Angewandte Chemie (International Ed. in English)
There has been growing interest in performing organocatalysis within a supramolecular system as a means of controlling reaction reactivity and stereoselectivity. Here, a protein is used as a host for iminium catalysis. A pyrrolidine moiety is covalen