{"id":20,"date":"2015-01-14T00:39:04","date_gmt":"2015-01-14T00:39:04","guid":{"rendered":"http:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/?page_id=20"},"modified":"2024-03-20T10:51:01","modified_gmt":"2024-03-20T10:51:01","slug":"publications","status":"publish","type":"page","link":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"

Independent and Collaborative Publications (Cardiff University):<\/h3>\n
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  1. “Accessing Highly Substituted Indoles via B(C6<\/sub>F5<\/sub>)3<\/sub>-Catalyzed Secondary Alkyl Group Transfer”<\/em>, S. A. Elsherbeni, R. L. Melen,* A. P. Pulis* and L. C. Morrill*,\u00a0J. Org. Chem.<\/em>, 2024,\u00a089<\/strong>, 4244-4248. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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    1. “Recent Advances in Catalysis using Organoborane Mediated Hydride Abstraction”<\/em>, J. P. Gillions, S. A. Elsherbeni, L. Winfrey, L. Yun, R. L. Melen*, L. C. Morrill* and A. P. Pulis*,\u00a0Synlett<\/em>, 2023,\u00a034<\/strong>, 2117-2128. [link<\/a><\/span>] [Invited contribution to celebrate the 60th anniversary of the Matteson homologation] [Highlighted in the 14th EuCheMS Young Investigators Workshop Special Issue]<\/span><\/strong><\/li>\n<\/ol>\n

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      1. “Nickel-Catalyzed Intramolecular Alkene Difunctionalization by Ball-Milling”<\/em>, M. T. J. Williams, L. C. Morrill* and D. L. Browne*,\u00a0Adv. Synth. Catal.<\/em>, 2023,\u00a0365<\/strong>, 1477-1484. [link<\/a><\/span>] [Hot Topic: Earth-Abundant Transition Metal Catalysis]<\/span><\/strong><\/li>\n<\/ol>\n

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        1. “Electrochemical Generation and Utilization of Alkoxy Radicals”<\/em>, A. A. M. A. El Gehani, H. A. Maashi, J. Harnedy and L. C. Morrill*, Chem. Commun.<\/i>, 2023,\u00a059<\/strong>, 3655-3664. [link<\/span><\/a>] [Part of themed collection:\u00a0Chemical Communications Hot Articles 2023]<\/span><\/strong><\/span><\/li>\n<\/ol>\n

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          1. “Deconstructive Functionalization of Unstrained Cycloalkanols via Electrochemically-Generated Aromatic Radical Cations”<\/em>, J. Harnedy, H. A. Maashi, A. A. M. A. El Gehani, M. Burns and L. C. Morrill*, Org. Lett<\/em>., 2023,\u00a025<\/strong>, 1486-1490. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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            1. “One-Pot Synthesis of Styrene Derivaties from Allyl Silanes via B(C6<\/sub>F5<\/sub>)3<\/sub>-Catalyzed Isomerization – Hiyama Coupling”<\/em>, B. A. Kustiana, R. L. Melen, and L. C. Morrill*, Org. Lett<\/em>., 2022,\u00a024<\/strong>, 8694-8697. [link<\/a><\/span>] [Highlighted in Chemistry Views<\/span><\/strong>]<\/span> <\/strong><\/span>[link<\/a><\/span>] [Highlighted in\u00a0Organic Chemistry Portal<\/em><\/span><\/strong>]<\/span><\/strong> [link]<\/a><\/span><\/span><\/li>\n<\/ol>\n

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              1. “Mechanical Activation of Zero-Valent Metal Reductants for Nickel-Catalyzed Cross-Electrophile Coupling”<\/em>, A. C. Jones\u2020, M. T. J. Williams\u2020, L. C. Morrill*, and D. L. Browne*, ACS Catal.<\/em>, 2022,\u00a012<\/strong>, 13681-13689. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                1. “B(C6<\/sub>F5<\/sub>)3<\/sub>-Catalyzed (E)-Selective Isomerization of Alkenes”<\/em>, B. A. Kustiana, S. A. Elsherbeni, T. G. Linford-Wood, R. L. Melen, M. N. Grayson and L. C. Morrill*, Chem. Eur. J.<\/em>, 2022,\u00a028<\/strong>, e202202454. [link<\/span><\/a>]<\/li>\n<\/ol>\n

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                  1. “Electrochemical Alkene Azidocyanation via 1,4-Nitrile Migration”<\/em>, A. C. Seastram, M. D. Hareram, T. M. B. Knight and L. C. Morrill*, Chem. Commun.<\/em>, 2022, 58<\/strong>, 8658-8662. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                    1. “Electrochemical Deconstructive Functionalization of Cycloalkanols via Alkoxy Radicals Enabled by Proton-Coupled Electron Transfer”<\/em>, M. Deepak Hareram, A. A. M. A. El Gehani, J. Harnedy, A. C. Seastram, A. C. Jones, M. Burns, T. Wirth, D. L. Browne and L. C. Morrill*, Org. Lett<\/em>, 2022,\u00a024<\/strong>, 3890-3895. [link<\/span><\/a>]<\/li>\n<\/ol>\n

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                      1. “Mechanochemical Organocatalysis: Do High Enantioselectivities Contradict what we Might Expect?”<\/em>, M. T. J. Williams, L. C. Morrill* and D. L. Browne*,\u00a0ChemSusChem<\/em>, 2022,\u00a015<\/strong>, e202102157. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                        1. “The Role of Streptavidin and its Variants in Catalysis by Biotinylated Secondary Amines”<\/em>, A. R. N\u00f6dling, N. Santi, R. Castillo, M. Lipka-Lloyd, Y. Jin, L. C. Morrill, K. Swiderek*, V. Moliner* and L. Y. P. Luk*, Org. Biomol. Chem.<\/em>, 2021,\u00a019<\/strong>, 10424-10431.\u00a0[link<\/a><\/span>]<\/li>\n<\/ol>\n

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                          1. “Electrochemical oxidative Z-selective C(sp2)-H chlorination of acrylamides”<\/em>, J. Harnedy, M. D. Hareram, G. J. Tizzard, S. J. Coles and L. C. Morrill*, Chem. Commun.<\/em>, 2021,\u00a057<\/strong>, 12643-12646.\u00a0<\/em>[link<\/span><\/a>] [Invited contribution to the 2021 Emerging Investigators themed collection]<\/span><\/strong><\/li>\n<\/ol>\n

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                            1. “Ball Milling Enabled Reactivity of Manganese Metal<\/i>“, W. I. Nicholson, J. L. Howard, G. Magri, A. C. Seastram, A. Khan, R. R. A. Bolt, L. C. Morrill, E. Richards and D. L. Browne*,\u00a0Angew. Chem. Int. Ed.<\/em>, 2021,\u00a060<\/strong>, 23128-23133. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                              1. “Borrowing Hydrogen for Organic Synthesis”, <\/em>B. G. Reed-Berendt,\u2020 D. E. Latham,\u2020 M. B. Dambatta and L. C. Morrill*,\u00a0ACS Cent. Sci.<\/em>, 2021,\u00a07<\/strong>, 570-585. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                1. “Electron deficient borane-mediated hydride abstraction in amines: stoichiometric and catalytic processes”,<\/em> S. Basak, L. Winfrey, B. A. Kustiana, R. L. Melen*, L. C. Morrill* and A. P. Pulis*, Chem. Soc. Rev.<\/em>, 2021,\u00a050<\/strong>, 3720-3737. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                  1. “Transfer Hydrogenations Catalyzed by Steptavidin-hosted Secondary Amine Organocatalyst<\/i>“, N. Santi, L. C. Morrill, K. Swiderek, V. Moliner and L. Y. P. Luk*,\u00a0Chem. Commun<\/em>., 2021,\u00a057<\/strong>, 1919-1922. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                    1. “Expedient Organocatalytic Aza-Morita-Baylis-Hillman Reaction Through Ball-Milling<\/i>“, M. T. J. Williams, L. C. Morrill* and D. L. Browne*,\u00a0ACS Sustainable Chem. Eng.<\/em>, 2020,\u00a08<\/strong>, 17876-17881. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                      1. “Transition Metal Free \u03b1-C-Alkylation of Ketones Using Secondary Alcohols<\/i>“, M. B. Dambatta, J. Santos, R. R. A. Bolt and L. C. Morrill*, Tetrahedron<\/em>, 2020, 76<\/strong>, 131571. [link<\/a><\/span>] [Invited contribution to the Special Issue on Strategies for Efficient Organic Synthesis Dedicated to the Achievements of Prof. Jonathan Williams]<\/span><\/strong><\/li>\n<\/ol>\n

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                                        1. “Streptavidin-hosted Organocatalytic Aldol Addition<\/em>“<\/em>, N. Santi, L. C. Morrill and L. Y. P. Luk*,\u00a0Molecules<\/em>, <\/em>2020, 25<\/strong>, 2457. [link<\/span><\/a>] [Invited contribution to the Hybrid Catalysts for Asymmetric Catalysis Special Issue]\u00a0<\/span><\/strong><\/li>\n<\/ol>\n

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                                          1. “B(C6<\/sub>F5<\/sub>)3<\/sub>-Catalyzed Direct C3 Alkylation of Indoles and Oxindoles”<\/em>, S. Basak, A. Alvarez-Montoya, L. Winfrey, R. L. Melen*, L. C. Morrill* and A. P. Pulis*, ACS Catal.,<\/em> 2020, 10<\/strong>, 4835-4840. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                            1. “Manganese-Catalyzed One-Pot Conversion of Nitroarenes into N-Methylarylamines Using Methanol<\/em>“, B. G. Reed-Berendt, N. Mast and L. C. Morrill*, Eur. J. Org. Chem.<\/em>, 2020, 1136-1140. [link<\/span><\/a>]<\/span> [Invited contribution to the YourJOC Talents Special Issue]\u00a0<\/span><\/strong><\/li>\n<\/ol>\n

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                                              1. “N-Heterocyclic Carbene Acyl Anion Organocatalysis by Ball-Milling<\/em>“, W. I. Nicholson, A. C. Seastram, S. A. Iqbal, B. G. Reed-Berendt, L. C. Morrill* and D. L. Browne*,\u00a0ChemSusChem<\/em>, 2020,\u00a013<\/strong>, 131-135. [link<\/a><\/span>] [Hot Topic: Organocatalysis]<\/span><\/strong><\/li>\n<\/ol>\n

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                                                1. “Manganese-Catalyzed Electrochemical Deconstructive Chlorination of Cycloalkanols via Alkoxy<\/em> Radicals”, B. D. W. Allen,\u2020 M. D. Hareram,\u2020 A. C. Seastram, T. McBride, T. Wirth, D. L. Browne* and L. C. Morrill*,\u00a0Org. Lett<\/em>., 2019, 21<\/strong>, 9241-9246. [link<\/a><\/span>] [Associated correction to citations]\u00a0<\/span><\/strong>[link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                                  1. “One-Pot Conversion of Allylic Alcohols to\u00a0<\/em>\u03b1-Methyl Ketones via Iron-Catalyzed Isomerization-Methylation<\/em>“, D. E. Latham, K. Polidano, J. M. J. Williams and L. C. Morrill*, Org. Lett.<\/em>, 2019, 21<\/strong>, 7914-7918. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                                    1. “Iron-Catalyzed Borrowing Hydrogen \u03b2-C(sp3<\/sup>)-Methylation of<\/em> Alcohols<\/em>“, K. Polidano, J. M. J. Williams and L. C. Morrill*, ACS Catal<\/em>., 2019,\u00a09<\/strong>, 8575-8580. [link<\/span><\/a>] [Highlighted in\u00a0Synfacts<\/em>, 2019,\u00a015<\/span><\/strong>, 1280]<\/span><\/strong> [link]<\/a><\/span><\/span><\/li>\n<\/ol>\n

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                                                      1. “Iron-Catalyzed Borrowing Hydrogen C-Alkylation of Oxindoles Using<\/em> Alcohols<\/em>“, M. B. Dambatta,\u00a0K. Polidano, A. D. Northey, J. M. J. Williams and L. C. Morrill*,\u00a0ChemSusChem<\/em>, 2019,\u00a012<\/strong>, 2345-2349. [link<\/span><\/a>]<\/li>\n<\/ol>\n

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                                                        1. “Manganese-Catalyzed N-Alkylation of Sulfonamides Using Alcohols<\/em>“, B. G. Reed-Berendt and L. C. Morrill*, J.\u00a0<\/em>Org. Chem.<\/em>, 2019,\u00a084<\/strong>, 3715-3724. [link<\/a><\/span>] [Highlighted in\u00a0Organic Chemistry Portal<\/em><\/span><\/strong>]<\/span><\/strong> [link]<\/a><\/span><\/span><\/li>\n<\/ol>\n

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                                                          1. “Recent Advances in Homogeneous Borrowing Hydrogen Catalysis using Earth-Abundant First Row Transition Metals”<\/em>, B. G. Reed-Berendt, K. Polidano and L. C. Morrill*,\u00a0Org. Biomol. Chem.<\/em>, 2019,\u00a017<\/strong>, 1595-1607. [link<\/a><\/span>]\u00a0[Invited contribution to the New Talent Special Issue]<\/span><\/strong><\/li>\n<\/ol>\n

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                                                            1. “FLP-Catalyzed Transfer Hydrogenation of Silyl Enol Ethers”<\/em>, I. Khan, B. G. Reed-Berendt, R. L. Melen* and L. C. Morrill*,\u00a0Angew. Chem. Int. Ed.<\/em>, 2018, 57<\/strong>, 12356-12359. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                                              1. “Synthesis and Reactivity of N-Allenyl Cyanamides”,<\/em>\u00a0J. N. Ayres, M. T. J. Williams, G. J. Tizzard, S. J. Coles, K. B. Ling and L. C. Morrill*, Org. Lett<\/em>., 2018,\u00a020<\/strong>, 5282-5285. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                                                1. “Reactivity and Selectivity of Iminium Organocatalysis Improved by a Protein Host”,<\/em>\u00a0A. R. N\u00f6dling, K. Swiderek, R. Castillo, J. W. Hall, A. Angelastro, L. C. Morrill, Y. Jin, Y-H. Tsai, V. Moliner* and L. Y. P. Luk*,\u00a0Angew. Chem. Int. Ed.<\/em>, 2018, 57<\/strong>, 12478-12482. [link<\/a><\/span>]<\/li>\n<\/ol>\n

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                                                                  1. \u201cIron-Catalyzed Methylation using the Borrowing Hydrogen Approach<\/em>\u201d, K. Polidano, B. D. W. Allen, J. M. J. Williams and L. C. Morrill*,\u00a0ACS Catal<\/em>.<\/em>, 2018,\u00a08<\/strong>, 6440-6445. [link<\/a>]<\/span><\/li>\n<\/ol>\n

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                                                                    1. \u201cExploring Tandem Ruthenium-Catalyzed Hydrogen Transfer and SNAr Chemistry<\/em>\u201d, K. Polidano, B. G. Reed-Berendt, A. Basset, A. J. A. Watson, J. M. J. Williams and L. C. Morrill*,\u00a0Org. Lett.<\/em>, 2017,\u00a019<\/strong>, 6716-6719. [link<\/span><\/a>]<\/li>\n<\/ol>\n

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                                                                      1. \u201cFrustrated Lewis Pair (FLP)-Catalyzed Hydrogenation of Aza-Morita-Baylis-Hillman Adducts and Sequential Organo-FLP Catalysis<\/em>\u201d, I. Khan, M. Manzotti, G. J. Tizzard, S. J. Coles, R. L. Melen* and L. C. Morrill*,\u00a0ACS Catal.<\/em>, 2017,\u00a07<\/strong>, 7748-7752. [link<\/span><\/a><\/span>]<\/li>\n<\/ol>\n

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                                                                        1. “Deoxycyanamidation of Alcohols with N-Cyano-N-Phenyl-p-Methylbenzenesulfonamide (NCTS)”,\u00a0<\/em>J. N. Ayres, M. W. Ashford, Y. St\u00f6ckl, V. Prudhomme, K. B. Ling, J. A. Platts and L. C. Morrill*,\u00a0Org. Lett.<\/em>, 2017,\u00a019<\/strong>, 3835-3838.\u00a0[link]<\/span><\/a><\/li>\n<\/ol>\n

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                                                                          1. “N-Cyanation of Secondary Amines using Trichloroacetonitrile”<\/em>,\u00a0J. N. Ayres, K. B. Ling* and L. C. Morrill*,\u00a0Org. Lett.<\/em>, 2016,\u00a018<\/strong>, 5528-5531. [link]<\/a><\/span><\/li>\n<\/ol>\n

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                                                                            Postdoctoral Publications (UC Berkeley with Prof. Richmond Sarpong):<\/h3>\n
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                                                                            1. “A Benzyne-Insertion Approach to Hetisine-Type Diterpenoid Alkaloids: Synthesis of Cossonidine (Davisine)”<\/em>, K. G. M. Kou, J. J. Pflueger, T. Kiho, L. C. Morrill<\/span>, E. L. Fisher, K. Clagg, T. P. Lebold, J. K. Kisunzu* and R. Sarpong*,\u00a0J. Am. Chem. Soc.<\/em>, 2018,\u00a0140<\/strong>, 8105-8109. [link<\/a><\/span>]\u00a0[Highlighted in\u00a0Synfacts<\/em>,\u00a02018, 14<\/i><\/span><\/strong>, 890]<\/span><\/strong> [link]<\/a><\/span><\/span><\/li>\n
                                                                            2. “A Magnesiate Addition\/Ring-Expansion Strategy to Access the 6-7-6 Tricyclic Core of Hetisine-type C20-Diterpenoid Alkaloids”,\u00a0<\/em>J. J. Pflueger, L. C. Morrill<\/span>, J. N. deGruyter, M. A. Perea and R. Sarpong*,\u00a0Org. Lett.<\/em>, 2017,\u00a019<\/strong>, 4632-4635. [link<\/span><\/a><\/span>]<\/li>\n
                                                                            3. \u201cPalladium-catalyzed \u03b2-Selective C(sp3)-H Arylation of N-Boc-Piperidines”,<\/em>\u00a0A. Millet and O. Baudoin*; checked by\u00a0<\/em>L. C. Morrill<\/span> and R. Sarpong,\u00a0Org. Synth.<\/em>, 2015, 92<\/b>, 76-90.\u00a0[link]<\/span><\/a><\/span><\/li>\n<\/ol>\n

                                                                              Postgraduate Publications (University of St Andrews with Prof. Andrew D. Smith):<\/h3>\n
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                                                                              1. “Catalytic Generation of Ammonium Enolates and Related Tertiary Amine-Derived Intermediates: Applications, Mechanism and Stereochemical Models (n\u2192\u03c0*)”,\u00a0<\/em>K. N. Van, L. C. Morrill<\/span>, A. D. Smith and D. Romo,\u00a0Book Chapter within “Lewis Base Catalysis in Organic Synthesis”,\u00a0<\/em>ed. E. Vedejs and S. E. Denmark, Wiley, Weinheim, 2016. [link]<\/a><\/span><\/i><\/li>\n
                                                                              2. “Enantioselective Synthesis of 3,5,6-Substituted Dihydropyranones and Dihydropyridinones using Isothiourea-Mediated Catalysis”,<\/i> D. G. Stark, L. C. Morrill<\/span>, D. B. Cordes, A. M. Z. Slawin, T. J. C. O’Riordan and A. D. Smith*,\u00a0Chem. Asian J.<\/em>, 2016, 11<\/strong>, 395-400.\u00a0[link]<\/a><\/span>\u00a0[Special Issue: Catalysis and Transformation of Complex Molecules]<\/span><\/strong><\/li>\n
                                                                              3. “Asymmetric Isothiourea-Catalysed Formal [3+2] Cycloadditions of Ammonium Enolates with Oxaziridines”<\/span><\/em>,\u00a0<\/span><\/span>S. R. Smith,\u00a0C. Fallan, J. E. Taylor,\u00a0R. McLennan,\u00a0D. S. B. Daniels,\u00a0L. C. Morrill<\/span>,\u00a0A. M. Z. Slawin and\u00a0A. D. Smith*,\u00a0Chem. Eur. J<\/em>., 2015, 21<\/strong>, 10530-10536.\u00a0[link]<\/span><\/a><\/span><\/span><\/li>\n
                                                                              4. \u201cOrganocatalytic Michael Addition-Lactonisation of Carboxylic Acids using \u03b1,\u03b2-Unsaturated Trichloromethyl Ketones as \u03b1,\u03b2-Unsaturated Ester Equivalents\u201d<\/em>, L. C. Morrill<\/span>, D. G. Stark, J. E. Taylor, S. R. Smith, J. A. Squires, A. C. A. D\u2019Hollander, C. Simal, P. Shapland, T. J. C. O\u2019Riordan and A. D. Smith*, Org. Biomol. Chem<\/em>., 2014, 12<\/strong>, 9016-9027. [link]<\/span><\/a>\u00a0[Highlighted in\u00a0Synfacts<\/em>,\u00a02015, 11<\/i><\/span><\/strong>, 315]<\/span><\/strong> [link]<\/a>\u00a0[Part of themed collection: 2014 Hot Articles in Organic and Biological Chemistry] <\/span><\/strong><\/span><\/span><\/span><\/span><\/li>\n
                                                                              5. \u201cOrganocatalytic Lewis base functionalisation of carboxylic acids and esters via ammonium\/azolium enolates\u201d<\/em>, L. C. Morrill<\/span> and A. D. Smith*, Chem. Soc. Rev.<\/em>, 2014, 43<\/strong>, 6214-6226.\u00a0[link]<\/a><\/span>\u00a0[One of the most accessed articles in Chem. Soc. Rev.<\/em> during June 2014]<\/span><\/strong><\/li>\n
                                                                              6. \u201cLewis Base Catalysed Asymmetric [2+2] Cycloadditions\u201d,\u00a0<\/em>A. D. Smith, J. Douglas, L. C. Morrill<\/span> and E. Richmond,\u00a0<\/span>Book Chapter within \u201cMethods and Applications of Cycloaddition Reactions in Organic Synthesis\u201d\u00a0<\/em>, ed. N. Nishiwaki, Wiley, New York, 2014.\u00a0[link]<\/a><\/span><\/li>\n
                                                                              7. \u201cIsothiourea-Mediated Asymmetric Functionalization of 3-Alkenoic Acids\u201d<\/em>, L. C. Morrill<\/span>, S. M. Smith, A. M. Z. Slawin and A. D. Smith*, J. Org. Chem.<\/em>, 2014, 79<\/strong>, 1640-1655.\u00a0<\/em>[link]<\/span><\/a><\/span><\/li>\n
                                                                              8. \u201c2-Arylacetic anhydrides as ammonium enolate precursors\u201d<\/em>, L. C. Morrill<\/span>, L. A. Ledingham, J-P. Couturier, J. Bickel, A. Harper, C. Fallan and A. D. Smith*, Org. Biomol. Chem.<\/em>, 2014, 12<\/strong>, 624-636. [link]<\/span><\/a><\/span><\/li>\n
                                                                              9. \u201cIsothiourea-Mediated One-Pot Synthesis of Functionalized Pyridines\u201d<\/em>, D. G. Stark, L. C. Morrill<\/span>, P-P. Yeh, A. M. Z. Slawin, T. J. C. O\u2019Riordan and A. D. Smith*, Angew. Chem. Int. Ed.<\/em>, 2013, 52<\/strong>, 11642-11646.\u00a0[link]<\/a><\/span>\u00a0<\/span>[Selected as a Hot Paper] [Highlighted in Synfacts<\/em>, 2013, 9<\/em>, 1344]<\/span><\/strong> [link]<\/span><\/a> <\/span>[Highlighted in Org. Chem. Highlights<\/em>, 2014, June 23]<\/span><\/strong>\u00a0[link]<\/span><\/a><\/span><\/span><\/li>\n
                                                                              10. \u201cStereospecific Asymmetric N-Heterocyclic Carbene (NHC)-Catalyzed Redox Synthesis of Trifluoromethyl Dihydropyranones and Mechanistic Insights\u201d<\/em>, A. T. Davies, J. E. Taylor, J. Douglas, C. J. Collett, L. C. Morrill<\/span>, C. Fallan, A. M. Z. Slawin and A. D. Smith*, J. Org. Chem.<\/em>, 2013, 78<\/strong>, 9243-9257. [link]<\/span><\/a><\/span><\/li>\n
                                                                              11. \u201cIsothiourea-mediated asymmetric Michael-lactonisation of trifluoromethylenones: a synthetic and mechanistic study\u201d<\/em>, L. C. Morrill<\/span>, J. Douglas, T. Lebl, D. J. Fox, A. M. Z. Slawin and A. D. Smith*, Chem. Sci.<\/em>, 2013,4<\/strong>, 4146-4155. [link]<\/a>\u00a0<\/span><\/span>[One of the most accessed articles in Chem. Sci.<\/em> during August 2013]\u00a0[Part of themed collection: Celebrating the 2014 RSC Prize and Award Winners] <\/strong><\/span><\/li>\n
                                                                              12. \u201cCatalytic asymmetric \u03b1<\/em>-amination of carboxylic acids using isothioureas\u201d<\/em>, L. C. Morrill<\/span>, T. Lebl, A. M. Z. Slawin and A. D. Smith*, Chem. Sci.<\/em>, 2012, 3<\/strong>, 2088-2093. [link]<\/span><\/a><\/span><\/li>\n
                                                                              13. \u201cOrganocatalytic Functionalisation of Carboxylic Acids: Isothiourea-Catalysed Asymmetric Intra- and Intermolecular Michael Addition-Lactonisations\u201d<\/em>, D. Belmessieri, L. C. Morrill<\/span>, C. Simal, A. M. Z. Slawin and A. D. Smith*, J. Am. Chem. Soc<\/em>., 2011, 133<\/strong>, 2714-2720. [link]<\/span><\/a><\/span>\u00a0[Highlighted in Synfacts<\/em>, 2011, 4<\/em>, 436]<\/span><\/strong>\u00a0[link]<\/span><\/a><\/span><\/span><\/li>\n<\/ol>\n

                                                                                Undergraduate Publications (University of St Andrews):<\/h3>\n
                                                                                  \n
                                                                                1. \u201cRegiodivergent Lewis base-promoted O- to C-carboxyl transfer of furanyl carbonates\u201d<\/em>, C. D. Campbell, C. Joannesse, L. C. Morrill<\/span>, D. Philp and A. D. Smith*, Org. Biomol. Chem.,\u00a0<\/em>2015, 13<\/strong>, 2895-2900. [link]<\/a>\u00a0[Part of themed collection: 2015 Hot Articles in Organic and Biomolecular Chemistry] <\/span><\/strong><\/span><\/span><\/li>\n
                                                                                2. \u201cEfficacious, inhaled PDE4 inhibitors with low emetic potential and long duration of action, for the treatment of COPD\u201d,<\/em> C. De Savi*, R. J. Cox*, D. Warner, A. R. Cook, M. R. Dickinson, A. McDonough, L. C. Morrill<\/span>, B. Parker, G. Andrews, S. Young, P. S. Gilmour, R. Riley and M. S. Dearman, J. Med. Chem.<\/em>, 2014, 57<\/strong>, 4661-4676.\u00a0<\/em>[link]<\/span><\/a><\/span><\/li>\n
                                                                                3. \u201cIsothiourea-Mediated Asymmetric O- to C-Carboxyl Transfer of Oxazoyl Carbonates: Structure-Selectivity Profiles and Mechanistic Studies\u201d<\/em>, C. Joannesse, C. P. Johnston, L. C. Morrill<\/span>, P. A. Woods, M. Kieffer, T. A. Nigst, H. Mayr, T. Lebl, D. Philp, R. A. Bragg and A. D. Smith*, Chem. Eur. J.<\/em>, 2012, 18<\/strong>, 2398-2408. [link]<\/span><\/a><\/span><\/li>\n
                                                                                4. \u201cIsothiourea-Catalyzed Asymmetric C-Acylation of Silyl Ketene Acetals\u201d<\/em>, P. A. Woods, L. C. Morrill<\/span>, R. A. Bragg and A. D. Smith*, Chem. Eur. J.<\/em>, 2011, 17<\/strong>, 11060-11067. [link]<\/span><\/a><\/span><\/li>\n
                                                                                5. \u201cIsothiourea-catalyzed asymmetric O- to C-carboxyl transfer of furanyl carbonates\u201d<\/em>, C. Joannesse, L. C. Morrill<\/span>, C. D. Campbell, A. M. Z. Slawin and A. D. Smith*, Synthesis<\/em>, 2011, 1865-1879. [link]<\/span><\/a><\/span><\/li>\n
                                                                                6. \u201cIsothiourea-Mediated Stereoselective C-acylation of Silyl Ketene Acetals\u201d<\/em>, P. A. Woods, L. C. Morrill<\/span>, T Lebl, A. M. Z. Slawin, R. A. Bragg and A. D. Smith*, Org. Lett<\/em>., 2010, 12<\/strong>, 2660-2663. [link]<\/span><\/a><\/span><\/li>\n
                                                                                7. \u201cUnexpected Rearrangement Leading to Formation of a 1,3-Bis(triphenylphosponio)prop-1-en-3-idyl Carboxylate\u201d<\/em>, R. A. Aitken*, L. P. Cleghorn, R. M. Leitch, L. C. Morrill<\/span> and A. M. Z. Slawin, Eur. J. Org. Chem<\/em>., 2010,\u00a03211-3214. [link]<\/span><\/a><\/span><\/li>\n
                                                                                8. \u201cN-heterocyclic carbene catalysed O- to C-carboxyl transfer of indolyl and benzofuranyl carbonates\u201d<\/em>, J. E. Thomson, A. F. Kyle, C. Concell\u00f3n, K. A. Gallagher, P. Lenden, L. C. Morrill<\/span>, A. J. Miller, C. Joannesse, A. M. Z. Slawin and A. D. Smith*, Synthesis<\/em>, 2008, 2805-2818. [link]<\/span><\/a><\/span><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"

                                                                                  Independent and Collaborative Publications (Cardiff University): “Accessing Highly Substituted Indoles via B(C6F5)3-Catalyzed Secondary Alkyl Group Transfer”, S. A. Elsherbeni, R. L. Melen,* A. P. Pulis* and L. C. Morrill*,\u00a0J. Org. Chem., 2024,\u00a089, 4244-4248. [link] “Recent Advances in Catalysis using Organoborane Mediated Hydride Abstraction”, J. P. Gillions, S. A. Elsherbeni, L. Winfrey, L. Yun, R. L. […]<\/p>\n","protected":false},"author":623,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-20","page","type-page","status-publish","hentry"],"jetpack_sharing_enabled":true,"meta_box":[],"_links":{"self":[{"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/pages\/20","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/users\/623"}],"replies":[{"embeddable":true,"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/comments?post=20"}],"version-history":[{"count":243,"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/pages\/20\/revisions"}],"predecessor-version":[{"id":2408,"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/pages\/20\/revisions\/2408"}],"wp:attachment":[{"href":"https:\/\/blogs.cardiff.ac.uk\/themorrillgroup\/wp-json\/wp\/v2\/media?parent=20"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}