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David M. Hodgson

Chemistry University of Oxford, Oxford, United Kingdom 
synthesis of biologically active molecules
"David M. Hodgson"

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Herman O. Sintim grad student 2002 Oxford
Christopher D. Bray grad student 2001-2005
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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
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