Photoisomerisation of dibenzobarrelenes - a facile route to polycyclic synthons

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DC Field	Value	Language
dc.contributor.author	Ramaiah, D	-
dc.contributor.author	Sajimon, M C	-
dc.contributor.author	Joshy Joseph	-
dc.contributor.author	George, M V	-
dc.date.accessioned	2015-10-01T04:39:01Z	-
dc.date.available	2015-10-01T04:39:01Z	-
dc.date.issued	2005	-
dc.identifier.citation	Chemical Society Reviews 34(1):48-57;Jan 2005	en_US
dc.identifier.issn	0306-0012	-
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/2069	-
dc.description.abstract	Triplet state mediated di-pi-methane rearrangements of dibenzobarrelenes give a variety of interesting synthons, formed as primary and secondary photoproducts. These synthons could find use for the synthesis of complex synthetic targets. This tutorial review highlights the photoisomerisation of some bridgehead substituted dibenzobarrelenes and the products derived from them. Selected examples of photoisomerisations proceeding through a tri-pi-methane pathway are also included.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Dibenzobarrelenes	en_US
dc.subject	Polycyclic synthons	en_US
dc.subject	Di-pi-methane	en_US
dc.subject	Photoisomerisation	en_US
dc.title	Photoisomerisation of dibenzobarrelenes - a facile route to polycyclic synthons	en_US
dc.type	Article	en_US
Appears in Collections:	2005

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