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

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DC Field	Value	Language
dc.contributor.author	Shukla, Matsyendranath	-
dc.contributor.author	Dorai, K.	-
dc.date.accessioned	2020-12-10T07:24:47Z	-
dc.date.available	2020-12-10T07:24:47Z	-
dc.date.issued	2013	-
dc.identifier.citation	Tetrahedron, 69(9), pp.2142-2149.	en_US
dc.identifier.other	https://doi.org/10.1016/j.tet.2013.01.002	-
dc.identifier.uri	https://www.sciencedirect.com/science/article/pii/S0040402013000203	-
dc.identifier.uri	http://hdl.handle.net/123456789/2963	-
dc.description	Only IISERM authors are available in the record.	-
dc.description.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.	en_US
dc.language.iso	en	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chromeno-2,6,9-trioxabicyclo[3.3.1]nonadienes	en_US
dc.subject	4-Chloro-3-formylcoumarin	en_US
dc.subject	o-Hydroxyacetophenones	en_US
dc.subject	DFT	en_US
dc.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	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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