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Visible Light-Mediated Cyclisation Reaction for the Synthesis of Highly-Substituted Tetrahydroquinolines and Quinolines.

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Title: Visible Light-Mediated Cyclisation Reaction for the Synthesis of Highly-Substituted Tetrahydroquinolines and Quinolines.
Authors: Sherborne GJ; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK., Kemmitt P; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK., Prentice C; Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.; EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK., Zysman-Colman E; Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK., Smith AD; EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK., Fallan C; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK.
Source: Angewandte Chemie (International ed. in English) [Angew Chem Int Ed Engl] 2023 Jan 09; Vol. 62 (2), pp. e202207829. Date of Electronic Publication: 2022 Dec 07.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-VCH Country of Publication: Germany NLM ID: 0370543 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1521-3773 (Electronic) Linking ISSN: 14337851 NLM ISO Abbreviation: Angew Chem Int Ed Engl Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Visible Light-Mediated Cyclisation Reaction for the Synthesis of Highly-Substituted Tetrahydroquinolines and Quinolines.
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  Data: <searchLink fieldCode="AU" term="%22Sherborne+GJ%22">Sherborne GJ</searchLink>; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK.<br /><searchLink fieldCode="AU" term="%22Kemmitt+P%22">Kemmitt P</searchLink>; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK.<br /><searchLink fieldCode="AU" term="%22Prentice+C%22">Prentice C</searchLink>; Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.; EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.<br /><searchLink fieldCode="AU" term="%22Zysman-Colman+E%22">Zysman-Colman E</searchLink>; Organic Semiconductor Centre, EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.<br /><searchLink fieldCode="AU" term="%22Smith+AD%22">Smith AD</searchLink>; EaStCHEM School of Chemistry, University of St Andrews, St Andrews, Fife, KY16 9ST, UK.<br /><searchLink fieldCode="AU" term="%22Fallan+C%22">Fallan C</searchLink>; Medicinal Chemistry Oncology R&D, Research and Early Development, AstraZeneca, Cambridge Science Park, Unit 310, Darwin Building, Cambridge, CB4 0WG, UK.
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  Data: <searchLink fieldCode="JN" term="%220370543%22">Angewandte Chemie (International ed. in English)</searchLink> [Angew Chem Int Ed Engl] 2023 Jan 09; Vol. 62 (2), pp. e202207829. <i>Date of Electronic Publication: </i>2022 Dec 07.
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