Alistair Boyer
Affiliations: | University of Glasgow, Glasgow, Scotland, United Kingdom |
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"Alistair Boyer"Parents
Sign in to add mentor| Andrew B. Holmes | research assistant | 2003-2004 | Cambridge |
| Steven Victor Ley | grad student | 2004-2008 | Cambridge |
| Mark Lautens | post-doc | 2009-2011 | University of Toronto |
| J Stephen Clark | research scientist | 2011-2014 | Glasgow University |
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| Williams MB, Wells RJ, Boyer A. (2022) Synthesis and reactivity of 1-sulfonylcyclooctatriazoles. Chemical Communications (Cambridge, England) |
| Williams MB, Boyer A. (2022) Modular Synthesis of Highly Substituted 3-Azapyrroles by Rh(II)-Catalyzed N-H Bond Insertion and Cyclodehydration. The Journal of Organic Chemistry |
| Boyer A. (2015) Enantioselective synthesis of (+)-petromyroxol, enabled by rhodium-catalyzed denitrogenation and rearrangement of a 1-sulfonyl-1,2,3-triazole. The Journal of Organic Chemistry. 80: 4771-5 |
| Clark JS, Romiti F, Hogg KF, et al. (2015) Synthesis of cyclopropyl-substituted furans by brønsted Acid promoted cascade reactions. Angewandte Chemie (International Ed. in English). 54: 5744-7 |
| Boyer A. (2014) Rhodium(II)-catalyzed stereocontrolled synthesis of 2-tetrasubstituted saturated heterocycles from 1-sulfonyl-1,2,3-triazoles. Organic Letters. 16: 5878-81 |
| Boyer A. (2014) Rhodium(II)-catalyzed stereocontrolled synthesis of dihydrofuran-3-imines from 1-tosyl-1,2,3-triazoles. Organic Letters. 16: 1660-3 |
| Clark JS, Boyer A, Aimon A, et al. (2012) Organocatalytic synthesis of highly substituted furfuryl alcohols and amines. Angewandte Chemie (International Ed. in English). 51: 12128-31 |
| Boyer A, Lautens M. (2011) Rhodium-catalyzed domino enantioselective synthesis of bicyclo[2.2.2]lactones. Angewandte Chemie (International Ed. in English). 50: 7346-9 |
| Webster R, Boyer A, Fleming MJ, et al. (2010) Practical asymmetric synthesis of bioactive aminotetralins from a racemic precursor using a regiodivergent resolution Organic Letters. 12: 5418-5421 |
| Boyer A, Veitch GE, Beckmann E, et al. (2009) Second-generation synthesis of azadirachtin: a concise preparation of the propargylic mesylate fragment. Angewandte Chemie (International Ed. in English). 48: 1317-20 |