Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2963
Title: Facile access to novel chromeno-2,6,9-trioxabicyclo[3.3.1]nonadienes via tandem nucleophilic substitution and [4+2] hetero Diels–Alder reaction: experimental and theoretical study
Authors: Shukla, Matsyendranath
Dorai, K.
Keywords: Chromeno-2,6,9-trioxabicyclo[3.3.1]nonadienes
4-Chloro-3-formylcoumarin
o-Hydroxyacetophenones
DFT
Issue Date: 2013
Publisher: Elsevier
Citation: Tetrahedron, 69(9), pp.2142-2149.
Abstract: An efficient synthesis of novel chromeno-2,6,9-trioxabicyclo-[3.3.1]nonadienes (CTOBN) scaffolds was achieved by mild base mediated reaction of 4-chloro-3-formylcoumarin and o-hydroxyacetophenones. The structure of the product was confirmed by X-ray analysis and the proposed mechanism was validated computationally at B3LYP/6-31G(d) level.
Description: Only IISERM authors are available in the record.
URI: https://www.sciencedirect.com/science/article/pii/S0040402013000203
http://hdl.handle.net/123456789/2963
Appears in Collections:Research Articles

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