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Title: A highly selective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis
Authors: Allin, Steven M.
Thomas, Christopher I.
Allard, James E.
Doyle, Kevin J.
Elsegood, Mark R.J.
Keywords: Natural products
Heterocycles
Lactams
Asymmetric synthesis
Issue Date: 2005
Publisher: © Wiley-VCH Verlag
Citation: ALLIN, S. et al., 2005. A highly selective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis. European Journal of Organic Chemistry, 19, pp.4179-4186.
Abstract: We present a facile and highly stereoselective approach to the indolo[2,3-a]quinolizine ring system from a readily available, non-racemic chiral template. We demonstrate the potential for application of this methodology to natural product synthesis through conversion of the template to some representative indole alkaloids with high enantiomeric purity in both enantiomeric series.
Description: This article has been published in the journal, European Journal of Organic Chemistry [© Wiley-VCH Verlag]. The definitive version, ALLIN, S. et al., 2005. A highly selective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis. European Journal of Organic Chemistry, 19, pp.4179-4186, is available at: https://doi.org/10.1002/ejoc.200500412.
URI: https://dspace.lboro.ac.uk/2134/654
Publisher Link: https://doi.org/10.1002/ejoc.200500412
ISSN: 1434-193X
Appears in Collections:Published Articles (Chemistry)

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