Peter Quayle, PhD
Affiliations: | Chemistry | University of Manchester, Manchester, England, United Kingdom |
Area:
Organometallics, Synthetic Methodology, Atom Transfer Reactions, Asymmetric Synthesis, Polymer ChemistryWebsite:
http://www.chemistry.manchester.ac.uk/aboutus/staff/show.html?ea=Peter.QuayleGoogle:
"Peter Quayle"Mean distance: 7.55 | S | N | B | C | P |
Parents
Sign in to add mentor| Anthony GM Barrett | grad student | Imperial College London | |
| Barry M. Trost | post-doc | UW Madison |
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Publications
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| Rashid SO, Almadhhi SS, Berrisford DJ, et al. (2019) Radical Truce-Smiles reactions on an isoxazole template: Scope and limitations Tetrahedron. 75: 2413-2430 |
| Rasheed OK, Quayle P. (2018) Azo-Dyes: New Palladium and Copper Catalysed Coupling Reactions on an Old Template Synthesis. 50: 2608-2616 |
| Tabatabaei Dakhili SY, Caslin SA, Faponle AS, et al. (2017) Recombinant silicateins as model biocatalysts in organosiloxane chemistry. Proceedings of the National Academy of Sciences of the United States of America |
| Price GA, Brisdon AK, Randall S, et al. (2017) Some insights into the gold-catalysed A 3 -coupling reaction Journal of Organometallic Chemistry. 846: 251-262 |
| Rasheed OK, Bawn C, Davies D, et al. (2017) The Synthesis of Group 10 and 11 Metal Complexes of 3,6,9‐Trithia‐1‐(2,6)‐pyridinacyclodecaphane and Their Use in A3‐Coupling Reactions European Journal of Organic Chemistry. 2017: 5252-5261 |
| Little MS, Yeates SG, Alwattar AA, et al. (2017) Front Cover: Insights into the Scholl Coupling Reaction: A Key Transformation of Relevance to the Synthesis of Graphenes and Related Systems (Eur. J. Org. Chem. 13/2017) European Journal of Organic Chemistry. 2017: 1674-1674 |
| Little MS, Yeates SG, Alwattar AA, et al. (2017) Insights into the Scholl Coupling Reaction: A Key Transformation of Relevance to the Synthesis of Graphenes and Related Systems European Journal of Organic Chemistry. 2017: 1694-1703 |
| Rasheed OK, Lawrence A, Quayle P, et al. (2016) A Modular Approach to Functionalised Dyes Synlett. 27: 905-911 |
| Christou S, Edwards AC, Pritchard RG, et al. (2016) Synthesis of hybrid natural product analogues with anti-tumour properties Tetrahedron. 72: 5433-5443 |
| Rasheed OK, Hardcastle IR, Raftery J, et al. (2015) Aryne generation vs. Truce-Smiles and fries rearrangements during the Kobayashi fragmentation reaction: a new bi-aryl synthesis. Organic & Biomolecular Chemistry. 13: 8048-52 |