Timothy J. Donohoe, D.Phil

Affiliations: 
Chemistry University of Oxford, Oxford, United Kingdom 
Area:
asymmetric synthesis and the application of stereoselective oxidation and reduction reactions to natural product synthesis
Website:
http://donohoe.chem.ox.ac.uk/
Google:
"Timothy J. Donohoe"
Bio:

http://research.chem.ox.ac.uk/timothy-donohoe.aspx

Mean distance: 8.27
 
SNBCP

Parents

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Steve G. Davies grad student 1989-1992 Oxford
 (Chiral Oxonium Ions)
Philip D. Magnus post-doc 1992-1994 UT Austin

Children

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​Nicholas J. Race research assistant 2009-2010 Oxford
Michael James Waring grad student
David  R. Carbery post-doc Oxford
Christopher R Jones post-doc Oxford
Herman O. Sintim post-doc 2002-2004 Oxford
Luiz Claudio Almeida Barbosa post-doc 2008-2009 Oxford
John F. Bower post-doc 2008-2010 Oxford
Ignacio Colomer post-doc 2014-2016
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Publications

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Aynetdinova D, Jaschinski M, Jenkins TC, et al. (2024) HFIP promoted carbo-lactonisation as a new route to functionalised lactones. Chemical Communications (Cambridge, England)
Bailey EP, Donohoe TJ, Smith MD. (2024) Functional group tolerant hydrogen borrowing C-alkylation. Nature Communications. 15: 5131
Crompton JL, Frost JR, Rowe SM, et al. (2023) Synthesis of Cyclopropanes via Hydrogen-Borrowing Catalysis. Organic Letters
Smith L, Armstrong R, Hou J, et al. (2023) Redox Reorganization: Aluminium Promoted 1,5-Hydride Shifts Allow the Controlled Synthesis of Multisubstituted Cyclohexenes. Angewandte Chemie (International Ed. in English). e202307424
Day AJ, Jenkins TC, Kischkewitz M, et al. (2023) Metal and Activating Group Free C-4 Alkylation of Isoquinolines via a Temporary Dearomatization Strategy. Organic Letters. 25: 614-618
Kischkewitz M, Marinic B, Kratena N, et al. (2022) Evolution of the Dearomative Functionalization of Activated Quinolines and Isoquinolines: Expansion of the Electrophile Scope. Angewandte Chemie (Weinheim An Der Bergstrasse, Germany). 134: e202204682
Kratena N, Marinic B, Donohoe TJ. (2022) Recent advances in the dearomative functionalisation of heteroarenes. Chemical Science. 13: 14213-14225
Aynetdinova D, Jacques R, Christensen K, et al. (2022) Alcohols as efficient intermolecular initiators for a highly stereoselective polyene cyclisation cascade. Chemistry (Weinheim An Der Bergstrasse, Germany)
Hoff O, Kratena N, Aynetdinova D, et al. (2022) A Vicinal Diol Approach for the Total Synthesis of Molestin E, ent-Sinulacembranolide A and ent-Sinumaximol A. Chemistry (Weinheim An Der Bergstrasse, Germany)
Cox L, Zhu Y, Smith P, et al. (2022) Alcohols as Alkylating Agents in the Cation Induced Formation of Nitrogen Heterocycles. Angewandte Chemie (International Ed. in English)
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