Jonathan M. Goodman
Affiliations: | Chemistry | University of Cambridge, Cambridge, England, United Kingdom |
Website:
http://www-jmg.ch.cam.ac.ukGoogle:
"Jonathan Goodman"Children
Sign in to add trainee| Robert S. Paton | grad student | 2005-2008 | Cambridge |
| Silvina Pellegrinet | post-doc |
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Publications
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| Lam CC, Goodman JM. (2023) Reaction dynamics as the missing puzzle piece: the origin of selectivity in oxazaborolidinium ion-catalysed reactions. Chemical Science. 14: 12355-12365 |
| Caballero-García G, Goodman JM. (2021) -Triflylphosphoramides: highly acidic catalysts for asymmetric transformations. Organic & Biomolecular Chemistry |
| Ermanis K, Colgan AC, Proctor RSJ, et al. (2020) A Computational and Experimental Investigation of the Origin of Selectivity in the Chiral Phosphoric Acid Catalyzed Enantioselective Minisci Reaction. Journal of the American Chemical Society |
| Ndukwe IE, Wang X, Lam NYS, et al. (2020) Synergism of anisotropic and computational NMR methods reveals the likely configuration of phormidolide A. Chemical Communications (Cambridge, England) |
| Lee S, Goodman JM. (2020) Rapid Route-Finding for Bifurcating Organic Reactions. Journal of the American Chemical Society |
| Wright D, Plajer AJ, Rizzuto FJ, et al. (2019) Guest Binding via N-H•••π-Bonding and Kinetic Entrapment by an Inorganic Macrocycle. Angewandte Chemie (International Ed. in English) |
| Ermanis K, Parkes KEB, Agback T, et al. (2019) The optimal DFT approach in DP4 NMR structure analysis - pushing the limits of relative configuration elucidation. Organic & Biomolecular Chemistry |
| Reid JP, Ermanis K, Goodman JM. (2019) BINOPtimal: a web tool for optimal chiral phosphoric acid catalyst selection. Chemical Communications (Cambridge, England) |
| Allen TEH, Grayson MN, Goodman JM, et al. (2018) Using Transition State Modelling to Predict Mutagenicity for Michael Acceptors. Journal of Chemical Information and Modeling |
| Han BY, Lam NYS, MacGregor CI, et al. (2018) A synthesis-enabled relative stereochemical assignment of the C1-C28 region of hemicalide. Chemical Communications (Cambridge, England) |