Mark G McLaughlin
Affiliations: | Manchester Metropolitan University, Manchester, England, United Kingdom |
Area:
Synthetic Methodology, Medicinal ChemistryGoogle:
"Mark McLaughlin"Mean distance: (not calculated yet)
Parents
Sign in to add mentor| Matthew J Cook | grad student | ||
| Julian Blagg | post-doc | ||
| Paul E. Brennan | post-doc |
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Publications
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| Roberts DD, McLaughlin MG. (2022) Diastereoselective access to substituted oxetanes hydrosilylation-iodocyclisation of homopropargylic alcohols. Chemical Communications (Cambridge, England) |
| Basson AJ, Halcovitch NR, McLaughlin MG. (2022) Unified Approach to Diverse Fused Fragments via Catalytic Dehydrative Cyclization. Chemistry (Weinheim An Der Bergstrasse, Germany) |
| Roberts DD, McLaughlin MG. (2021) Regioselective Synthesis of Multifunctional Allylic Amines; Access to Ambiphilic Aziridine Scaffolds. Organic Letters. 23: 4463-4467 |
| Basson AJ, McLaughlin MG. (2021) Sustainable Access to 5-Amino-Oxazoles and Thiazoles via Calcium-Catalyzed Elimination-Cyclization with Isocyanides. Chemsuschem |
| Patel NR, Nawrat CC, McLaughlin M, et al. (2020) Synthesis of Islatravir Enabled by a Catalytic, Enantioselective Alkynylation of a Ketone. Organic Letters |
| Basson AJ, McLaughlin MG. (2020) Synthesis of Functionalized Isoindolinones via Calcium Catalyzed Generation and Trapping of -Acyliminium Ions. The Journal of Organic Chemistry. 85: 5615-5628 |
| Britten TK, McLaughlin MG. (2020) Brønsted Acid Catalyzed Peterson Olefinations. The Journal of Organic Chemistry. 85: 301-305 |
| Basson AJ, McLaughlin MG. (2019) Functionalisation of isoindolinones via a calcium catalysed Hosomi-Sakurai allylation. Chemical Communications (Cambridge, England). 55: 8317-8320 |
| Le Bihan YV, Lanigan RM, Atrash B, et al. (2019) C8-substituted pyrido[3,4-d]pyrimidin-4(3H)-ones: Studies towards the identification of potent, cell penetrant Jumonji C domain containing histone lysine demethylase 4 subfamily (KDM4) inhibitors, compound profiling in cell-based target engagement assays. European Journal of Medicinal Chemistry. 177: 316-337 |
| Kiely-Collins HJ, Sechi I, Brennan PE, et al. (2018) Mild, calcium catalysed Beckmann rearrangements. Chemical Communications (Cambridge, England). 54: 654-657 |