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Methods for the synthesis of annulated pyrroles via cyclisation strategies
Citation
Olivier, WJ and Smith, JA and Bissember, AC, Methods for the synthesis of annulated pyrroles via cyclisation strategies, Organic and Biomolecular Chemistry, 16, (8) pp. 1216-1226. ISSN 1477-0520 (2018) [Refereed Article]
Copyright Statement
© The Royal Society of Chemistry 2018
Abstract
Pyrrole, pyrrolidine, and indolizidine alkaloids represent important classes of natural products. Historically, these heterocycles and their derivatives have been the focus of significant interest in organic synthesis. In this report, we review the methods that have been employed to synthesise annulated pyrroles via transformations that include: Friedel–Crafts acylations and alkylations, Michael additions, Heck couplings, hydroarylations, carbenoid insertions, and radical cyclisations.
Item Details
Item Type: | Refereed Article |
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Keywords: | pyrrole, organic synthesis, methodology, heterocyclic chemistry |
Research Division: | Chemical Sciences |
Research Group: | Organic chemistry |
Research Field: | Organic chemical synthesis |
Objective Division: | Expanding Knowledge |
Objective Group: | Expanding knowledge |
Objective Field: | Expanding knowledge in the chemical sciences |
UTAS Author: | Olivier, WJ (Mr Wesley Olivier) |
UTAS Author: | Smith, JA (Associate Professor Jason Smith) |
UTAS Author: | Bissember, AC (Associate Professor Alex Bissember) |
ID Code: | 124510 |
Year Published: | 2018 |
Web of Science® Times Cited: | 35 |
Deposited By: | Chemistry |
Deposited On: | 2018-02-23 |
Last Modified: | 2019-12-03 |
Downloads: | 0 |
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