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Portrait of Dr Wesley Moran Dr Wesley Moran

w.j.moran@hud.ac.uk | 01484 473741



Biography

Wes was born in Birmingham. He obtained his MChem and PhD (2004) under the supervision of Professor Joe Harrity at the University of Sheffield. He then spent two years at The University of North Carolina at Chapel Hill in Professor Jim Morken’s group followed by 17 months at The University of Manchester in Professor Jonathan Clayden’s group. He began his independent career in September 2007 as a Lecturer in Organic Chemistry at the University of Huddersfield and in August 2009 was promoted to Senior Lecturer.

Research & Scholarship

The Moran Group

We are based in the Department of Chemistry at the University of Huddersfield. Our research is in the field of synthetic organic chemistry and we are particularly interested in polyvalent iodine compounds, C-H activation and the synthesis of small molecules.

For further details, please see the Moran Group page

Publications and Other Research Outputs

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hindrance from relatively simple diyne and alkyne precursors. The diarylmethanes made in this way show no evidence in their NMR spectra, however, of rotational restriction.', 'creators_id' => 'w.j.moran@hud.ac.uk', 'contributors_name_lineage' => undef, 'userid' => '6', 'patent_applicant' => undef, 'monograph_type' => undef, 'datestamp_minute' => '9', 'lyricists_name_family' => undef, 'sword_slug' => undef, 'id_number' => 'doi:10.1039/b700353f', 'volume' => '5', 'gscholar_datestamp_month' => undef, 'conductors_id' => undef, 'suggestions' => undef, 'referencetext' => undef, 'date_year' => '2007', 'status_changed_hour' => '14', 'gscholar_cluster' => undef, 'producers_name_family' => undef }, '20364' => { 'funders' => undef, 'conductors_name_family' => undef, 'num_pieces' => undef, 'department' => undef, 'contributors_id' => undef, 'gscholar_datestamp_second' => undef, 'keywords' => undef, 'lyricists_name_lineage' => undef, 'lyricists_id' => undef, 'edit_lock_since' => '1409825824', 'creatorlist' => { '1' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Moran', 'eprintid' => '20364', 'creators_name_honourific' => '', 'pos' => '1', 'creators_name_given' => 'Wesley J.', 'creators_id' => 'w.j.moran@hud.ac.uk' }, '0' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Hamnett', 'eprintid' => '20364', 'creators_name_honourific' => '', 'pos' => '0', 'creators_name_given' => 'David J.', 'creators_id' => undef } }, 'exhibitors_id' => undef, 'latitude' => undef, 'replacedby' => undef, 'status_changed_month' => '5', 'editors_name_honourific' => undef, 'admin_note' => undef, 'event_title' => undef, 'date_type' => 'published', 'pres_type' => undef, 'longitude' => undef, 'creators_name_honourific' => '', 'include_in_hebci' => 'no', 'producers_name_honourific' => undef, 'scopus_citation_count' => undef, 'datestamp_year' => '2014', 'fileinfo' => '/style/images/fileicons/application_pdf.png;/20364/1/c4ob00556b.pdf', 'status_changed_second' => '33', 'exhibitors_name_honourific' => undef, 'editors_id' => undef, 'title' => 'Improving alkynyl(aryl)iodonium salts: 2-anisyl as a superior aryl group', 'corp_creators' => undef, 'contributors_name_given' => undef, 'alt_title' => undef, 'contributors_name_family' => undef, 'sponsors' => undef, 'output_media' => undef, 'editors_name_lineage' => undef, 'dir' => 'disk0/00/02/03/64', 'overlay_journal_id' => undef, 'gscholar_datestamp_year' => undef, 'ispublished' => 'pub', 'item_issues_count' => '0', 'conductors_name_given' => undef, 'sword_depositor' => undef, 'full_text_status' => 'public', 'lastmod_minute' => '18', 'refereed' => 'TRUE', 'contact_email' => 'w.j.moran@hud.ac.uk', 'copyright_holders' => undef, 'date_day' => undef, 'gscholar_impact' => undef, 'official_url' => 'http://dx.doi.org/10.1039/C4OB00556B', 'succeeds' => undef, 'datestamp_month' => '5', 'commentary' => undef, 'lastmod_day' => '4', 'publisher' => 'Royal Society of Chemistry', 'pagerange' => '4156-4162', 'include_in_pedagogical' => 'no', 'task_purpose' => undef, 'status_changed_year' => '2014', 'book_title' => undef, 'thesis_name' => undef, 'event_location' => undef, 'type' => 'article', 'publication' => 'Organic & Biomolecular Chemistry', 'lastmod_second' => '43', 'place_of_pub' => undef, 'contributors_name_honourific' => undef, 'gscholar_datestamp_day' => undef, 'issn' => '1477-0520', 'datestamp_hour' => '15', 'exhibitors_name_given' => undef, 'creators_name_family' => 'Moran', 'composition_type' => undef, 'producers_id' => undef, 'datestamp_second' => '33', 'note' => undef, 'edit_lock_until' => '0', 'editor_note' => undef, 'pedagogic_type' => undef, 'date_month' => 5, 'rights' => undef, 'contributors_type' => undef, 'scopus_id' => undef, 'eprintid' => '20364', 'producers_name_given' => undef, 'thesis_type' => undef, 'projects' => undef, 'lastmod_year' => '2014', 'data_type' => undef, 'gscholar_datestamp_minute' => undef, 'editors_name_given' => undef, 'isbn' => undef, 'include_in_cv' => 'yes', 'editors_name_family' => undef, 'lastmod_month' => '9', 'event_dates' => undef, 'fulltimestamp' => '20140500', 'learning_level' => undef, 'conductors_name_lineage' => undef, 'pages' => undef, 'source' => undef, 'lastmod_hour' => '10', 'number' => undef, 'rev_number' => '9', 'edit_lock_user' => '3483', 'series' => undef, 'creators_name_lineage' => '', 'pos' => '0', 'metadata_visibility' => 'show', 'eprint_status' => 'archive', 'creators_name_given' => 'Wesley J.', 'exhibitors_name_lineage' => undef, 'divisions' => 'sas', 'institution' => undef, 'subjects' => 'QD', 'gscholar_datestamp_hour' => undef, 'producers_name_lineage' => undef, 'lyricists_name_given' => undef, 'completion_time' => undef, 'status_changed_minute' => '22', 'conductors_name_honourific' => undef, 'exhibitors_name_family' => undef, 'lyricists_name_honourific' => undef, 'event_type' => undef, 'importid' => undef, 'status_changed_day' => '23', 'datestamp_day' => '23', 'abstract' => 'The majority of alkynyl(aryl)iodonium salts reported in the literature are derived from iodobenzene. This article describes the effects of varying this iodoarene building block on the synthesis, reactivity and stability of these salts. Two procedures to synthesize a variety of known and novel alkynyl(aryl)iodonium tosylates directly from the iodoarene are reported. In the reactions of these salts, those derived from 2-iodoanisole gave superior results than the others tested in every reaction. Isothermal microcalorimetry indicated that these novel salts were significantly more stable and less prone to decomposition than all of the other derivatives.', 'creators_id' => 'w.j.moran@hud.ac.uk', 'contributors_name_lineage' => undef, 'userid' => '3494', 'patent_applicant' => undef, 'monograph_type' => undef, 'datestamp_minute' => '22', 'lyricists_name_family' => undef, 'sword_slug' => undef, 'id_number' => 'doi:10.1039/C4OB00556B', 'volume' => '12', 'gscholar_datestamp_month' => undef, 'conductors_id' => undef, 'suggestions' => undef, 'referencetext' => undef, 'date_year' => '2014', 'status_changed_hour' => '15', 'gscholar_cluster' => undef, 'producers_name_family' => undef }, '19887' => { 'funders' => undef, 'conductors_name_family' => undef, 'num_pieces' => undef, 'department' => undef, 'contributors_id' => undef, 'gscholar_datestamp_second' => undef, 'keywords' => undef, 'lyricists_name_lineage' => undef, 'lyricists_id' => undef, 'edit_lock_since' => '1395932341', 'creatorlist' => { '1' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Moran', 'eprintid' => '19887', 'creators_name_honourific' => '', 'pos' => '1', 'creators_name_given' => 'Wesley J.', 'creators_id' => 'w.j.moran@hud.ac.uk' }, '0' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Aborways', 'eprintid' => '19887', 'creators_name_honourific' => '', 'pos' => '0', 'creators_name_given' => 'Marwa M.', 'creators_id' => 'U0863483@hud.ac.uk' } }, 'exhibitors_id' => undef, 'latitude' => undef, 'replacedby' => undef, 'status_changed_month' => '3', 'editors_name_honourific' => undef, 'admin_note' => undef, 'event_title' => undef, 'date_type' => undef, 'pres_type' => undef, 'longitude' => undef, 'creators_name_honourific' => '', 'include_in_hebci' => 'no', 'producers_name_honourific' => undef, 'scopus_citation_count' => undef, 'datestamp_year' => '2014', 'fileinfo' => '', 'status_changed_second' => '11', 'exhibitors_name_honourific' => undef, 'editors_id' => undef, 'title' => 'Reactions of tertiary propargyl alcohols with sodium halides under oxidative conditions ', 'corp_creators' => undef, 'contributors_name_given' => undef, 'alt_title' => undef, 'contributors_name_family' => undef, 'sponsors' => undef, 'output_media' => undef, 'editors_name_lineage' => undef, 'dir' => 'disk0/00/01/98/87', 'overlay_journal_id' => undef, 'gscholar_datestamp_year' => undef, 'ispublished' => 'pub', 'item_issues_count' => '0', 'conductors_name_given' => undef, 'sword_depositor' => undef, 'full_text_status' => 'none', 'lastmod_minute' => '59', 'refereed' => 'TRUE', 'contact_email' => 'w.j.moran@hud.ac.uk', 'copyright_holders' => undef, 'date_day' => 26, 'gscholar_impact' => undef, 'official_url' => 'http://dx.doi.org/10.1016/j.tetlet.2014.02.042', 'succeeds' => undef, 'datestamp_month' => '3', 'commentary' => undef, 'lastmod_day' => '27', 'publisher' => 'Elsevier', 'pagerange' => '2127-2129', 'include_in_pedagogical' => 'no', 'task_purpose' => undef, 'status_changed_year' => '2014', 'book_title' => undef, 'thesis_name' => undef, 'event_location' => undef, 'type' => 'article', 'publication' => 'Tetrahedron Letters', 'lastmod_second' => '11', 'place_of_pub' => undef, 'contributors_name_honourific' => undef, 'gscholar_datestamp_day' => undef, 'issn' => '0040-4039', 'datestamp_hour' => '14', 'exhibitors_name_given' => undef, 'creators_name_family' => 'Moran', 'composition_type' => undef, 'producers_id' => undef, 'datestamp_second' => '11', 'note' => undef, 'edit_lock_until' => '0', 'editor_note' => undef, 'pedagogic_type' => undef, 'date_month' => 3, 'rights' => undef, 'contributors_type' => undef, 'scopus_id' => undef, 'eprintid' => '19887', 'producers_name_given' => undef, 'thesis_type' => undef, 'projects' => undef, 'lastmod_year' => '2014', 'data_type' => undef, 'gscholar_datestamp_minute' => undef, 'editors_name_given' => undef, 'isbn' => undef, 'include_in_cv' => 'yes', 'editors_name_family' => undef, 'lastmod_month' => '3', 'event_dates' => undef, 'fulltimestamp' => '20140326', 'learning_level' => undef, 'conductors_name_lineage' => undef, 'pages' => undef, 'source' => undef, 'lastmod_hour' => '14', 'number' => '13', 'rev_number' => '6', 'edit_lock_user' => '6', 'series' => undef, 'creators_name_lineage' => '', 'pos' => '0', 'metadata_visibility' => 'show', 'eprint_status' => 'archive', 'creators_name_given' => 'Wesley J.', 'exhibitors_name_lineage' => undef, 'divisions' => 'sas', 'institution' => undef, 'subjects' => 'QD', 'gscholar_datestamp_hour' => undef, 'producers_name_lineage' => undef, 'lyricists_name_given' => undef, 'completion_time' => undef, 'status_changed_minute' => '59', 'conductors_name_honourific' => undef, 'exhibitors_name_family' => undef, 'lyricists_name_honourific' => undef, 'event_type' => undef, 'importid' => undef, 'status_changed_day' => '27', 'datestamp_day' => '27', 'abstract' => 'The study of the reactions of tertiary propargyl alcohols with sodium halides under oxidative conditions is presented. With sodium iodide, ?-iodoenones were formed, however, with sodium bromide or chloride the ?-haloenones were only formed in low yields under anhydrous conditions. Conversely, upon addition of water to the reaction mixtures, ?,?-dibromoketones and ?,?-dichloroketones were formed in good yields, but ?,?-diiodoketones were not observed', 'creators_id' => 'w.j.moran@hud.ac.uk', 'contributors_name_lineage' => undef, 'userid' => '918', 'patent_applicant' => undef, 'monograph_type' => undef, 'datestamp_minute' => '59', 'lyricists_name_family' => undef, 'sword_slug' => undef, 'id_number' => '10.1016/j.tetlet.2014.02.042', 'volume' => '55', 'gscholar_datestamp_month' => undef, 'conductors_id' => undef, 'suggestions' => undef, 'referencetext' => undef, 'date_year' => '2014', 'status_changed_hour' => '14', 'gscholar_cluster' => undef, 'producers_name_family' => undef }, '4037' => { 'funders' => undef, 'conductors_name_family' => undef, 'num_pieces' => undef, 'department' => undef, 'contributors_id' => undef, 'gscholar_datestamp_second' => undef, 'keywords' => undef, 'lyricists_name_lineage' => undef, 'lyricists_id' => undef, 'edit_lock_since' => undef, 'creatorlist' => { '1' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Moran', 'eprintid' => '4037', 'creators_name_honourific' => '', 'pos' => '1', 'creators_name_given' => 'Wesley J.', 'creators_id' => 'w.j.moran@hud.ac.uk' }, '0' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Hedley', 'eprintid' => '4037', 'creators_name_honourific' => '', 'pos' => '0', 'creators_name_given' => 'Simon J.', 'creators_id' => undef }, '3' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Harrity', 'eprintid' => '4037', 'creators_name_honourific' => '', 'pos' => '3', 'creators_name_given' => 'Joseph P. A.', 'creators_id' => undef }, '2' => { 'creators_name_lineage' => '', 'creators_name_family' => 'Price', 'eprintid' => '4037', 'creators_name_honourific' => '', 'pos' => '2', 'creators_name_given' => 'David A.', 'creators_id' => undef } }, 'exhibitors_id' => undef, 'latitude' => undef, 'replacedby' => undef, 'status_changed_month' => '4', 'editors_name_honourific' => undef, 'admin_note' => undef, 'event_title' => undef, 'date_type' => undef, 'pres_type' => undef, 'longitude' => undef, 'creators_name_honourific' => '', 'include_in_hebci' => 'no', 'producers_name_honourific' => undef, 'scopus_citation_count' => undef, 'datestamp_year' => '2009', 'fileinfo' => '', 'status_changed_second' => '24', 'exhibitors_name_honourific' => undef, 'editors_id' => undef, 'title' => 'Development of a [3+3] Cycloaddition Strategy toward Functionalized Piperidines', 'corp_creators' => undef, 'contributors_name_given' => undef, 'alt_title' => undef, 'contributors_name_family' => undef, 'sponsors' => undef, 'output_media' => undef, 'editors_name_lineage' => undef, 'dir' => 'disk0/00/00/40/37', 'overlay_journal_id' => undef, 'gscholar_datestamp_year' => undef, 'ispublished' => 'pub', 'item_issues_count' => '0', 'conductors_name_given' => undef, 'sword_depositor' => undef, 'full_text_status' => 'none', 'lastmod_minute' => '40', 'refereed' => 'TRUE', 'contact_email' => undef, 'copyright_holders' => undef, 'date_day' => undef, 'gscholar_impact' => undef, 'official_url' => 'http://dx.doi.org/10.1021/jo030002c', 'succeeds' => undef, 'datestamp_month' => '4', 'commentary' => undef, 'lastmod_day' => '2', 'publisher' => 'The American Chemical Society', 'pagerange' => '4286-4292', 'include_in_pedagogical' => 'no', 'task_purpose' => undef, 'status_changed_year' => '2009', 'book_title' => undef, 'thesis_name' => undef, 'event_location' => undef, 'type' => 'article', 'publication' => 'The Journal of Organic Chemistry', 'lastmod_second' => '26', 'place_of_pub' => undef, 'contributors_name_honourific' => undef, 'gscholar_datestamp_day' => undef, 'issn' => '00223263', 'datestamp_hour' => '10', 'exhibitors_name_given' => undef, 'creators_name_family' => 'Moran', 'composition_type' => undef, 'producers_id' => undef, 'datestamp_second' => '24', 'note' => undef, 'edit_lock_until' => undef, 'editor_note' => undef, 'pedagogic_type' => undef, 'date_month' => 5, 'rights' => undef, 'contributors_type' => undef, 'scopus_id' => undef, 'eprintid' => '4037', 'producers_name_given' => undef, 'thesis_type' => undef, 'projects' => undef, 'lastmod_year' => '2009', 'data_type' => undef, 'gscholar_datestamp_minute' => undef, 'editors_name_given' => undef, 'isbn' => undef, 'include_in_cv' => 'yes', 'editors_name_family' => undef, 'lastmod_month' => '6', 'event_dates' => undef, 'fulltimestamp' => '20030500', 'learning_level' => undef, 'conductors_name_lineage' => undef, 'pages' => undef, 'source' => undef, 'lastmod_hour' => '12', 'number' => '11', 'rev_number' => '9', 'edit_lock_user' => undef, 'series' => undef, 'creators_name_lineage' => '', 'pos' => '1', 'metadata_visibility' => 'show', 'eprint_status' => 'archive', 'creators_name_given' => 'Wesley J.', 'exhibitors_name_lineage' => undef, 'divisions' => 'sas', 'institution' => undef, 'subjects' => 'QD', 'gscholar_datestamp_hour' => undef, 'producers_name_lineage' => undef, 'lyricists_name_given' => undef, 'completion_time' => undef, 'status_changed_minute' => '34', 'conductors_name_honourific' => undef, 'exhibitors_name_family' => undef, 'lyricists_name_honourific' => undef, 'event_type' => undef, 'importid' => undef, 'status_changed_day' => '24', 'datestamp_day' => '24', 'abstract' => 'This paper describes a novel route to functionalized piperidines via a formal [3+3] cycloaddition reaction of activated aziridines and palladium?trimethylenemethane (Pd-TMM) complexes. The cycloaddition reaction generally proceeds enantiospecifically with ring opening at the least hindered site of the aziridine. Therefore, readily available enantiomerically pure 2-substituted aziridines can be utilized to prepare enantiomerically pure 2-substituted piperidines in good to excellent yield. The N-substituent on the aziridine proved to be crucial to the success of this reaction with only 4-toluenesulfonyl (Ts) and 4-methoxybenzenesulfonyl (PMBS) aziridines permitting smooth cycloaddition to take place. Additionally, spirocyclic aziridines have been found to participate in the [3+3] cycloaddition reaction, whereas 2,3-disubstituted aziridines can be applied to provide fused bicyclic piperidines, albeit in low yield.', 'creators_id' => 'w.j.moran@hud.ac.uk', 'contributors_name_lineage' => undef, 'userid' => '3494', 'patent_applicant' => undef, 'monograph_type' => undef, 'datestamp_minute' => '34', 'lyricists_name_family' => undef, 'sword_slug' => undef, 'id_number' => '10.1021/jo030002c', 'volume' => '68', 'gscholar_datestamp_month' => undef, 'conductors_id' => undef, 'suggestions' => undef, 'referencetext' => undef, 'date_year' => '2003', 'status_changed_hour' => '10', 'gscholar_cluster' => undef, 'producers_name_family' => undef } };

2014

Hamnett, D. and Moran, W. (2014) ‘Improving alkynyl(aryl)iodonium salts: 2-anisyl as a superior aryl groupOrganic & Biomolecular Chemistry , 12, pp. 4156-4162. ISSN 1477-0520

Aborways, M. and Moran, W. (2014) ‘Reactions of tertiary propargyl alcohols with sodium halides under oxidative conditions Tetrahedron Letters , 55 (13), pp. 2127-2129. ISSN 0040-4039

Alhalib, A. and Moran, W. (2014) ‘CuI-catalyzed cycloisomerization of propargyl amidesOrganic & Biomolecular Chemistry , 12 (5), pp. 795-800. ISSN 1477-0520

2013

Kayamba, F., Dunnill, C., Hamnett, D., Rodríguez, A., Georgopoulos, N. and Moran, W. (2013) ‘Piperolein B, isopiperolein B and piperamide C9:1(8E): total synthesis and cytotoxicitiesRSC Advances , 3 (37), pp. 16681-16685. ISSN 2046-2069

Rodríguez, A. and Moran, W. (2013) ‘Oxidative Rearrangement of Tertiary Propargylic AlcoholsSynlett , 24 (1), pp. 102-104. ISSN 0936-5214

2012

Moran, W. and Rodriguez, A. (2012) ‘Hypoiodous acid initiated rearrangement of tertiary propargylic alcohols to ?-iodoenonesOrganic & Biomolecular Chemistry , 10 (43), pp. 8590-8592. ISSN 1477-0520

Moran, W., MacRory, K. and Rodriguez, A. (2012) ‘Oxidative rearrangement of indoles to oxindolesRSC Advances , 2 (24), pp. 8962-8964. ISSN 2046-2069

Rodríguez, A. and Moran, W. (2012) ‘Chiral Aryl Iodide-Catalyzed Enantioselective ?-Oxidation of Ketones Synthesis , 44 (8), pp. 1178-1182. ISSN 00397881

Moran, W. and Rodríguez, A. (2012) ‘Metal-catalyzed Furan Synthesis. A ReviewOrganic Preparations and Procedures International , 44 (2), pp. 103-130. ISSN 0030-4948

2011

Moran, W. and Rodriguez, A. (2011) ‘An oxidative Hosomi-Sakurai strategy toward the synthesis of illioliganones B and CRSC Advances , 1 (1), p. 33. ISSN 2046-2069

Rodriguez, A. and Moran, W. (2011) ‘Iodobenzene-Catalyzed Intramolecular Oxidative Cyclization Reactions of ?-Alkynyl ?-KetoestersOrganic Letters , 13 (9), pp. 2220-2223. ISSN 15237060

Rodriguez, A. and Moran, W. (2011) ‘Furan synthesis through AuCl3-catalysed cycloisomerisation of ?-alkynyl ?-ketoestersTetrahedron Letters , 52 (20), pp. 2605-2607. ISSN 0040-4039

2010

Rodriguez, A. and Moran, W. (2010) ‘The Nitrile Functionality as a Directing Group in the Palladium-Catalysed Addition of Aryl Boronic Acids to Alkynes Letters in Organic Chemistry , 7 (1), pp. 7-10. ISSN 1570-1786

2009

Clayden, J., Moran, W., Edwards, P. and LaPlante, S. (2009) ‘The Challenge of Atropisomerism in Drug DiscoveryAngewandte Chemie International Edition , 48 (35), pp. 6398-6401. ISSN 14337851

Rodriguez, A., Fennessy, R. and Moran, W. (2009) ‘Palladium-catalysed direct alkenylation of sydnonesTetrahedron Letters , 50 (27), pp. 3942-3944. ISSN 0040-4039

Rodriguez, A. and Moran, W. (2009) ‘Palladium-Catalyzed Three-Component Coupling Reactions: 1,1-Difunctionalization of Activated Alkenes European Journal of Organic Chemistry , 2009 (9), pp. 1313-1316. ISSN 1434-193X

Rodriguez, A. and Moran, W. (2009) ‘Palladium-catalysed direct arylation of sydnonesSynthesis , 2009 (4), pp. 650-654. ISSN 00397881

2008

Clayden, J., Worrall, C., Moran, W. and Helliwell, M. (2008) ‘Enantioselective synthesis of an atropisomeric diaryl etherAngewandte Chemie International Edition , 47 (17), pp. 3234-3237. ISSN 14337851

2007

Clayden, J. and Moran, W. (2007) ‘Synthesis of densely functionalised arenes using [2 + 2 + 2] cycloaddition reactionsOrganic & Biomolecular Chemistry , 5 (7), p. 1028. ISSN 14770520

2006

Clayden, J. and Moran, W. (2006) ‘The Twisted Amide 2-Quinuclidone: 60 Years in the MakingAngewandte Chemie International Edition , 45 (43), pp. 7118-7120. ISSN 14337851

Moran, W. and Morken, J. (2006) ‘Rh-catalyzed enantioselective hydrogenation of vinyl boronates for the construction of secondary boronic estersOrganic Letters , 8 (11), pp. 2413-2419. ISSN 15237060

2005

Goodenough, K., Moran, W., Raubo, P. and Harrity, J. (2005) ‘Development of a Flexible Approach to Nuphar Alkaloids via Two Enantiospecific Piperidine-Forming ReactionsThe Journal of Organic Chemistry , 70 (1), pp. 207-213. ISSN 00223263

2003

Moran, W., Goodenough, K., Raubo, P. and Harrity, J. (2003) ‘A Concise Asymmetric Route to Nuphar Alkaloids. A Formal Synthesis of (?)-DeoxynupharidineOrganic Letters , 5 (19), pp. 3427-3429. ISSN 15237060

Hedley, S., Moran, W., Price, D. and Harrity, J. (2003) ‘Development of a [3+3] Cycloaddition Strategy toward Functionalized PiperidinesThe Journal of Organic Chemistry , 68 (11), pp. 4286-4292. ISSN 00223263

2002

Wybrow, R., Johnson, L., Auffray, B., Moran, W., Adams, H. and Harrity, J. (2002) ‘Unusual macrocyclic spirocycles from tandem metathesis reactions Tetrahedron Letters , 43 (44), pp. 7851-7854. ISSN 0040-4039

2001

Hedley, S., Moran, W., Prenzel, A., Price, D. and Harrity, J. (2001) ‘Synthesis of Functionalised Piperidines Through a [3 + 3] Cycloaddition StrategySynlett (10), pp. 1596-1598. ISSN 09365214

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Good
Satisfactory
Needs improvement

Excellent
Good
Satisfactory
Needs improvement

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