Kimber, MC and Lee, DS ORCID: https://orcid.org/0000-0002-8288-1838, 2024. The Kornblum DeLaMare rearrangement in natural product synthesis: 25 years of innovation. Natural Product Reports. ISSN 0265-0568
Full text not available from this repository.Abstract
Since its initial disclosure in 1951, the Kornblum DeLaMare rearrangement has proved an important synthetic transformation and has been widely adopted as a biomimetic step in natural product synthesis. Utilising the base catalysed decomposition of alkyl peroxides to yield a ketone and alcohol has found use in many syntheses as well as a key strategic step, including the unmasking of furans, as a biomimetic synthetic tool, and the use of the rearrangement to install oxygen enantioselectively. Since ca. 1998, its impact as a synthetic transformation has grown significantly, especially given the frequency of use in natural product syntheses, therefore this 25 year time period will be the focus of the review.
Item Type: | Journal article |
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Publication Title: | Natural Product Reports |
Creators: | Kimber, M.C. and Lee, D.S. |
Publisher: | Royal Society of Chemistry (RSC) |
Date: | 31 January 2024 |
ISSN: | 0265-0568 |
Identifiers: | Number Type 10.1039/d3np00058c DOI 1865568 Other |
Divisions: | Schools > School of Science and Technology |
Record created by: | Jeremy Silvester |
Date Added: | 22 Feb 2024 09:44 |
Last Modified: | 22 Feb 2024 09:44 |
URI: | https://irep.ntu.ac.uk/id/eprint/50915 |
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