Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Harvey J. A. Dale"'
Publikováno v:
Dale, H J A, Nottingham, C, Poree, C & Lloyd-Jones, G C 2021, ' Systematic Evaluation of 1,2-Migratory Aptitude in Alkylidene Carbenes ', Journal of the American Chemical Society, vol. 143, no. 4, pp. 2097-2107 . https://doi.org/10.1021/jacs.0c12400
Dale, H, Nottingham, C, Poree, C & Lloyd-Jones, G 2021, ' Systematic Evaluation of 1,2-Migratory Aptitude in Alkylidene Carbenes ', Journal of the American Chemical Society, vol. 143, no. 4, pp. 2097-2107 . https://doi.org/10.1021/jacs.0c12400
Dale, H, Nottingham, C, Poree, C & Lloyd-Jones, G 2021, ' Systematic Evaluation of 1,2-Migratory Aptitude in Alkylidene Carbenes ', Journal of the American Chemical Society, vol. 143, no. 4, pp. 2097-2107 . https://doi.org/10.1021/jacs.0c12400
Alkylidene carbenes undergo rapid inter- and intramolecular reactions and rearrangements, including 1,2-migrations of β-substituents to generate alkynes. Their propensity for substituent migration exerts profound influence over the broader utility o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6e236f84c531fe65674eae3315cd05f
https://hdl.handle.net/20.500.11820/8ffc77c5-716e-4b45-b242-140ea203a6e1
https://hdl.handle.net/20.500.11820/8ffc77c5-716e-4b45-b242-140ea203a6e1
Publikováno v:
Koyama, D, Dale, H J A & Orr-Ewing, A J 2018, ' Ultrafast Observation of a Photoredox Reaction Mechanism : Photoinitiation in Organocatalyzed Atom-Transfer Radical Polymerization ', Journal of the American Chemical Society, vol. 140, no. 4, pp. 1285-1293 . https://doi.org/10.1021/jacs.7b07829
Photoredox catalysis has driven a revolution in the field of organic chemistry, but direct mechanistic insights into reactions of genuine synthetic utility remain relatively scarce. Herein we report ultrafast time-resolved spectroscopic observation o
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:
Proceedings of the 73rd International Symposium on Molecular Spectroscopy.
Autor:
Costil, Romain1, Dale, Harvey J. A.1, Fey, Natalie1, Whitcombe, George1, Matlock, Johnathan V.1 johnathan.matlock@bristol.ac.uk, Clayden, Jonathan1 j.clayden@bristol.ac.uk
Publikováno v:
Angewandte Chemie. Oct2017, Vol. 129 Issue 41, p12707-12711. 5p.
Autor:
Orr-Ewing, Andrew J.
Publikováno v:
Structural Dynamics; 2019, Vol. 6 Issue 1, pN.PAG-N.PAG, 6p
Publikováno v:
Faraday Discussions; 2018, Vol. 211, p3-8, 6p
Publikováno v:
Faraday Discussions; 2018, Vol. 211, p569-591, 23p