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Peter K. Dornan

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2012 Chemistry University of California, Irvine, Irvine, CA 
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"Peter Dornan"
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Vy Maria Dong grad student 2013 University of Toronto
 (Transition metal catalysis: Construction of chiral lactones, ketones, sulfoxides and 6-deoxyerythronolide B.)
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Publications

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Dai XJ, Krolikowski P, Murray JI, et al. (2022) Synthesis of Substituted Pyridines via Formal (3+3) Cycloaddition of Enamines with Unsaturated Aldehydes and Ketones. The Journal of Organic Chemistry
Dornan PK, Lee D, Grubbs RH. (2016) Tandem Olefin Metathesis/Oxidative Cyclization: Synthesis of Tetrahydrofuran Diols from Simple Olefins. Journal of the American Chemical Society. 138: 6372-5
Dornan PK, Wickens ZK, Grubbs RH. (2015) Tandem Z-Selective Cross-Metathesis/Dihydroxylation: Synthesis of anti-1,2-Diols. Angewandte Chemie (International Ed. in English). 54: 7134-8
Herbert MB, Suslick BA, Liu P, et al. (2015) Cyclometalated Z-Selective Ruthenium Metathesis Catalysts with Modified N-Chelating Groups Organometallics. 34: 2858-2869
Hartung J, Dornan PK, Grubbs RH. (2014) Enantioselective olefin metathesis with cyclometalated ruthenium complexes. Journal of the American Chemical Society. 136: 13029-37
Dornan PK, Kou KG, Houk KN, et al. (2014) Dynamic kinetic resolution of allylic sulfoxides by Rh-catalyzed hydrogenation: a combined theoretical and experimental mechanistic study. Journal of the American Chemical Society. 136: 291-8
Dornan PK, Longobardi LE, Stephan DW. (2014) Reversible frustrated lewis pair addition of n-heterocycles to unsaturated c-c bonds Synlett. 25: 1521-1524
Dornan PK, Leung PL, Dong VM. (2011) Synthesis of C3- and C2-symmetric tris- and bis-sulfoxide ligands by asymmetric oxidation Tetrahedron. 67: 4378-4384
Laliberté S, Dornan PK, Chen A. (2010) Palladium-catalyzed double allylic alkylation of indole-2-hydroxamates: easy access to pyrazino[1,2-a]indole derivatives Tetrahedron Letters. 51: 363-366
Yeung CS, Dornan PK, Dong VM. (2010) Transition Metal Catalyzed Approaches to Lactones Involving C-O Bond Formation Catalyzed Carbon-Heteroatom Bond Formation. 35-68
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