Webb, NJ, Raw, SA and Marsden, SP orcid.org/0000-0002-2723-8954 (2018) Isoquinoline synthesis by C-H activation/annulation using vinyl acetate as an acetylene equivalent. Tetrahedron, 74 (38). pp. 5200-5205. ISSN 0040-4020
Abstract
Vinyl acetate is used as an acetylene equivalent in rhodium(III)-catalysed C-H activation/annulation with aryl ketoxime esters. Extension to an aldoxime ester allows for a concise formal synthesis of decumbenine B.
Metadata
| Item Type: | Article |
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| Authors/Creators: |
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| Copyright, Publisher and Additional Information: | (c) 2018, Elsevier Ltd. All rights reserved. This is an author produced version of a paper published in Tetrahedron. Uploaded in accordance with the publisher's self-archiving policy. |
| Keywords: | C-H activation; Heterocyclic synthesis; Isoquinoline; Alkaloid |
| Dates: |
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| Institution: | The University of Leeds |
| Academic Units: | The University of Leeds > Faculty of Engineering & Physical Sciences (Leeds) > School of Chemistry (Leeds) |
| Depositing User: | Symplectic Publications |
| Date Deposited: | 09 Jul 2018 16:22 |
| Last Modified: | 25 May 2019 00:41 |
| Status: | Published |
| Publisher: | Elsevier |
| Identification Number: | 10.1016/j.tet.2018.05.063 |
| Open Archives Initiative ID (OAI ID): | oai:eprints.whiterose.ac.uk:133029 |

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