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Participation of compact planar 1,3,5-tri(buta-2,3-dien-1-yl)-1,3,5- triazinane-2,4,6-trione in Pd(0) catalysed seven component cascade reactions delivers novel tunable molecular architecture

Gültekin, Zeynep, Elboray, Elghareeb E., Aly, Moustafa F., Abbas-Temirek, Hussien H., Shepherd, Helena J., Grigg, Ronald (2014) Participation of compact planar 1,3,5-tri(buta-2,3-dien-1-yl)-1,3,5- triazinane-2,4,6-trione in Pd(0) catalysed seven component cascade reactions delivers novel tunable molecular architecture. Tetrahedron, 70 (33). pp. 4934-4941. ISSN 0040-4020. (doi:10.1016/j.tet.2014.05.025) (The full text of this publication is not currently available from this repository. You may be able to access a copy if URLs are provided)

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Official URL
http://www.dx.doi.org/10.1016/j.tet.2014.05.025

Abstract

We report the spatially controlled, protecting group free, catalytic assembly of a library of nineteen 7-component cascade products generated from a novel planar trisallenyl 1,3,5-triazinane-2,4,6-trione core in combination with aryl iodides and amines with excellent regio and good stereoaselectivity for Z,Z,Z-isomers. © 2014 Elsevier Ltd. All rights reserved.

Item Type: Article
DOI/Identification number: 10.1016/j.tet.2014.05.025
Uncontrolled keywords: Palladium, stereoselective, tunable, multidirectional, peptides
Subjects: Q Science > QD Chemistry > QD478 Solid State Chemistry
Q Science > QD Chemistry > QD473 Physical properties in relation to structure
Divisions: Faculties > Sciences > School of Physical Sciences > Functional Materials Group
Depositing User: Giles Tarver
Date Deposited: 19 Oct 2015 08:08 UTC
Last Modified: 29 May 2019 16:06 UTC
Resource URI: https://kar.kent.ac.uk/id/eprint/50813 (The current URI for this page, for reference purposes)
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