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Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/13935

Title: An Au(I)-catalysed allenamide cyclisation giving access to an α-vinyl-substituted tetrahydroisoquinoline building block
Authors: Singh, Sanjitpal
Elsegood, Mark R.J.
Kimber, Marc C.
Keywords: Alkaloids
Allenamide
Tetrahydroisoquinoline
Au(I) catalysis
Diastereoselective
Issue Date: 2012
Publisher: © Georg Thieme Verlag
Citation: SINGH, S., ELSEGOOD, M.R.J. and KIMBER, M.C., 2012. An Au(I)-catalysed allenamide cyclisation giving access to an α-vinyl-substituted tetrahydroisoquinoline building block. Synlett, 23 (4), pp. 565 - 568
Abstract: An Au(I)-catalysed intramolecular hydroarylation of an enantiopure allenamide has been achieved and has given access to a key α-vinyl- substititued tetrahydroisoquinoline. Additionally this has been accomplished in very high yield and high diastereoselectivity. © Georg Thieme Verlag Stuttgart · New York.
Description: This article was published in the journal, Synlett [© Georg Thieme Verlag]. The definitive version is available at: http://dx.doi.org/10.1055/s-0031-1290335
Version: Accepted for publication
DOI: 10.1055/s-0031-1290335
URI: https://dspace.lboro.ac.uk/2134/13935
Publisher Link: http://www.thieme-connect.com
ISSN: 0936-5214
Appears in Collections:Published Articles (Chemistry)

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