Michael J Porter

University College London, London, United Kingdom 
Organic Synthesis
"Michael Porter"
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Jack E. Baldwin grad student 1992-1996 Oxford
Philip D. Magnus post-doc 1996-1998 UT Austin
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Coomber C, Porter M, Aliev A, et al. (2020) Tuning Reactivity in Pd‐catalysed C(sp3)‐H Arylations via Directing Group Modifications and Solvent Selection Advanced Synthesis & Catalysis
Laserna V, Porter MJ, Sheppard TD. (2019) Gold-Catalyzed Hydroamination of Propargylic Alcohols: Controlling Divergent Catalytic Reaction Pathways to Access 1,3-Aminoalcohols, 3-Hydroxyketones or 3-Aminoketones. The Journal of Organic Chemistry
Coomber CE, Laserna V, Martin LT, et al. (2019) Catalytic direct amidations in tert-butyl acetate using B(OCHCF). Organic & Biomolecular Chemistry
Gendron T, Sander K, Cybulska K, et al. (2018) Ring-Closing Synthesis of Dibenzothiophene Sulfonium Salts and Their Use as Leaving Groups for Aromatic F-Fluorination. Journal of the American Chemical Society
Coomber CE, Benhamou L, Bučar DK, et al. (2017) Silver-Free Palladium-Catalyzed C(sp3)-H Arylation of Saturated Bicyclic Amine Scaffolds. The Journal of Organic Chemistry
Foster RW, Benhamou L, Porter MJ, et al. (2015) Irreversible endo-selective diels-alder reactions of substituted alkoxyfurans: a general synthesis of endo-cantharimides. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 6107-14
Aliev AE, Arendorf JR, Pavlakos I, et al. (2015) Surfing π clouds for noncovalent interactions: arenes versus alkenes. Angewandte Chemie (International Ed. in English). 54: 551-5
Chavda JK, Procopiou PA, Horton PN, et al. (2014) Synthetic Studies Towards the Core Structure of Nakadomarin A by a Thioamide-Based Strategy. European Journal of Organic Chemistry. 2014: 129-139
Ellwood AR, Mortimer AJ, Goodman JM, et al. (2013) Reversal of facial selectivity in a thia-Claisen rearrangement by incorporation of a vinylic bromine substituent. Organic & Biomolecular Chemistry. 11: 7530-9
Anderson JC, Kalogirou AS, Porter MJ, et al. (2013) Synthesis of the reported structure of piperazirum using a nitro-Mannich reaction as the key stereochemical determining step. Beilstein Journal of Organic Chemistry. 9: 1737-44
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