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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Fleming MJ, Hodgson DM. (2021) Allylic alcohols and amines by carbenoid eliminative cross-coupling using epoxides or aziridines. Beilstein Journal of Organic Chemistry. 17: 2385-2389 |
Delany PK, Mortimer CL, Hodgson DM. (2020) Electrophile dependent mechanisms in the asymmetric trapping of α-lithio--(-butoxythiocarbonyl)azetidine. Chemical Communications (Cambridge, England) |
Hodgson DM, Almohseni HAA. (2020) Evolution of a Cycloaddition–Rearrangement Approach to the Squalestatins: A Quarter-Century Odyssey Synlett |
Delany PK, Hodgson DM. (2019) Synthesis and Homologation of an Azetidin-2-yl Boronic Ester with α-Lithioalkyl Triisopropylbenzoates. Organic Letters |
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 |
Almohseni HAA, Fegheh-Hassanpour Y, Arif T, et al. (2019) Alkene Ozonolysis in the Presence of Diazo Functionality: Accessing an Intermediate for Squalestatin Synthesis Synthesis. 51: 4231-4238 |
Sintim HO, Valade A, Harling DC, et al. (2019) Squarate desymmetrisation–ozonolysis as an approach to β-substituted-α-ketosuccinates and squalestatin synthesis Tetrahedron. 75: 130747 |
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 |