A highly selective synthesis of the indolo[2,3-a]quinolizine ring system and application to natural product synthesis
journal contribution
posted on 2006-01-06, 10:29 authored by Steven M. Allin, Christopher I. Thomas, James E. Allard, Kevin J. Doyle, Mark ElsegoodMark ElsegoodWe 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.
History
School
- Science
Department
- Chemistry
Pages
291914 bytesCitation
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.Publisher
© Wiley-VCH VerlagPublication date
2005Notes
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.ISSN
1434-193XPublisher version
Language
- en
