David M. Hodgson
Affiliations: | Chemistry | University of Oxford, Oxford, United Kingdom |
Area:
synthesis of biologically active moleculesWebsite:
http://hodgson.chem.ox.ac.uk/DavidMHodgson.htmGoogle:
"David M. Hodgson"Bio:
http://research.chem.ox.ac.uk/david-hodgson.aspx
Mean distance: 9.06 | S | N | B | C | P |
Children
Sign in to add traineeHerman O. Sintim | grad student | 2002 | Oxford |
Christopher D. Bray | grad student | 2001-2005 |
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Publications
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Sintim HO, Al Mamari HH, Almohseni HAA, et al. (2019) Alkylation of lithiated dimethyl tartrate acetonide with unactivated alkyl halides and application to an asymmetric synthesis of the 2,8-dioxabicyclo[3.2.1]octane core of squalestatins/zaragozic acids. Beilstein Journal of Organic Chemistry. 15: 1194-1202 |
Fegheh-Hassanpour Y, Arif T, Sintim HO, et al. (2018) Correction to Synthesis of (-)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition-Rearrangement and Cross-electrophile Coupling. Organic Letters |
Almohseni HAA, Al Mamari HH, Valade A, et al. (2018) Alkene protection against acid using a bromide substituent: application in a total synthesis of (-)-6,7-dideoxysqualestatin H5. Chemical Communications (Cambridge, England) |
Fegheh-Hassanpour Y, Ebrahim F, Arif T, et al. (2018) On the ozonolysis of unsaturated tosylhydrazones as a direct approach to diazocarbonyl compounds. Organic & Biomolecular Chemistry |
Fegheh-Hassanpour Y, Arif T, Sintim HO, et al. (2017) Synthesis of (-)-6,7-Dideoxysqualestatin H5 by Carbonyl Ylide Cycloaddition-Rearrangement and Cross-electrophile Coupling. Organic Letters |
Hodgson DM, Salik S. (2016) Utility of unsaturated terminal epoxides in cyclopropane synthesis Current Organic Chemistry. 20: 4-18 |
Jackson KE, Mortimer CL, Odell B, et al. (2015) α- and α'-Lithiation-Electrophile Trapping of N-Thiopivaloyl and N-tert-Butoxythiocarbonyl α-Substituted Azetidines: Rationalization of the Regiodivergence Using NMR and Computation. The Journal of Organic Chemistry. 80: 9838-46 |
Kuprov I, Hodgson DM, Kloesges J, et al. (2015) Anomalous nuclear Overhauser effects in carbon-substituted aziridines: scalar cross-relaxation of the first kind. Angewandte Chemie (International Ed. in English). 54: 3697-701 |
Hodgson DM, Mortimer CL, McKenna JM. (2015) Amine protection/α-activation with the tert-butoxythiocarbonyl group: application to azetidine lithiation-electrophilic substitution. Organic Letters. 17: 330-3 |
Hodgson DM, Man S, Powell KJ, et al. (2014) Intramolecular oxonium ylide formation-[2,3] sigmatropic rearrangement of diazocarbonyl-substituted cyclic unsaturated acetals: a formal synthesis of hyperolactone C. The Journal of Organic Chemistry. 79: 9728-34 |