Please use this identifier to cite or link to this item: https://dspace.iiti.ac.in/handle/123456789/9380
Title: Cycloaddition of cyclohexa-2,4-dienones with β-nitroacrylates: A short and efficient entry into bicyclo[2.2.2]octanes endowed with β-nitro-ester and β-amino ester functionality
Authors: Mobin, Shaikh M.
Keywords: acrylic acid derivative;alkadiene;beta amino ester;beta nitro ester;beta nitroacrylate derivative;bicyclo[2.2.2]octane derivative;cyclohexa 2,4 dienone derivative;ester derivative;unclassified drug;absorption;Article;cycloaddition;Diels Alder reaction;stereochemistry;stereoisomerism;Alnus
Issue Date: 2014
Publisher: Elsevier Ltd
Citation: Behera, T. K., Nurul Islam, S., Mobin, S. M., & Singh, V. (2014). Cycloaddition of cyclohexa-2,4-dienones with β-nitroacrylates: A short and efficient entry into bicyclo[2.2.2]octanes endowed with β-nitro-ester and β-amino ester functionality. Tetrahedron Letters, 55(37), 5170-5173. doi:10.1016/j.tetlet.2014.07.097
Abstract: Regio- and stereoselective cycloaddition of β-nitroacrylates with electron deficient cyclohexa-2,4-dienones leading to highly functionalised bicyclo[2.2.2]octanes having the β-nitroester group and their transformation to bicyclo[2.2.2]octanes having β-aminoester functionality is described. © 2014 Elsevier Ltd. All rights reserved.
URI: https://doi.org/10.1016/j.tetlet.2014.07.097
https://dspace.iiti.ac.in/handle/123456789/9380
ISSN: 0040-4039
Type of Material: Journal Article
Appears in Collections:Department of Chemistry

Files in This Item:
There are no files associated with this item.


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

Altmetric Badge: