Photoisomerisation of dibenzobarrelenes - a facile route to polycyclic synthons

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