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
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Publications

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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
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)
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 (International Ed. in English). e202204682
Hall CJJ, Marriott IS, Christensen KE, et al. (2022) Extension of hydrogen borrowing alkylation reactions for the total synthesis of (-)-γ-lycorane. Chemical Communications (Cambridge, England)
Haughey MB, Christensen KE, Poole DL, et al. (2021) Development of an enolate alkynylation approach towards the synthesis of the taiwanschirin natural products. Chemical Science. 12: 13392-13397
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