Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/654

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
Elsegood, Mark R.J.
Keywords: natural products
heterocycles
lactams
asymmetric synthesis
Issue Date: 2005
Publisher: © Wiley-VCH Verlag
Citation: ALLIN, S.A., THOMAS, C.I., ALLARD, J.E., DOYLE, K. and ELSEGOOD, M.R.J., 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.A., THOMAS, C.I., ALLARD, J.E., DOYLE, K. and ELSEGOOD, M.R.J., 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: http://www.interscience.wiley.com/jpages/1434-193X.
URI: https://dspace.lboro.ac.uk/2134/654
ISSN: 1434-193X
Appears in Collections:Published Articles (Chemistry)

Files associated with this item:

File Description SizeFormat
SMAIR-1.pdf313.14 kBAdobe PDFView/Open

 

SFX Query

Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.