Hilton, ST;
Jones, K;
(2007)
The tandem radical route to indole alkaloids: an unusual rearrangement reaction.
Arkivoc
, 2007
(XI)
120 - 128.
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Abstract
Cyclisation of the precursor 6 under standard radical conditions yields the tetracyclic structure 7 which represents the core of a number of indole alkaloids along with the novel tetracycle 13.
| Type: | Article |
|---|---|
| Title: | The tandem radical route to indole alkaloids: an unusual rearrangement reaction |
| Open access status: | An open access version is available from UCL Discovery |
| Publisher version: | http://www.arkat-usa.org/get-file/23095/ |
| Language: | English |
| Additional information: | Copyright is held by the authors and ARKAT USA, Inc. |
| Keywords: | Indoles, radical cyclisation, rearrangement, alkaloids |
| UCL classification: | UCL UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy UCL > Provost and Vice Provost Offices > School of Life and Medical Sciences > Faculty of Life Sciences > UCL School of Pharmacy > Pharma and Bio Chemistry |
| URI: | https://discovery.ucl.ac.uk/id/eprint/1353074 |
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