Photochemical rearrangement of calix[4]arene-derived bis(spirodienones): Formation of a new macrocycle

dc.contributor.author	Luxmi Varma, R
dc.contributor.author	Ganga, V B
dc.contributor.author	Suresh, E
dc.date.accessioned	2014-04-17T11:19:38Z
dc.date.available	2014-04-17T11:19:38Z
dc.date.issued	2007
dc.identifier.citation	Journal of Organic Chemistry 72(3):1017-1019;2 Feb 2007	en_US
dc.identifier.issn	0022-3263
dc.identifier.uri	http://ir.niist.res.in:8080/jspui/handle/123456789/1338
dc.description.abstract	Bis(spirodienones) of calix[4]arene undergo a facile photochemical rearrangement leading to a new macrocycle having a spirocyclic cyclopentenone-THF unit, a trisubstituted phenol, and a benzofuran moiety. The macrocyclic ring system has a 14-membered irregular cavity and resembles a partial bowl in the solid state.	en_US
dc.language.iso	en	en_US
dc.publisher	American Chemical Society	en_US
dc.subject	Derivatives	en_US
dc.subject	Calix[4]arene	en_US
dc.subject	Cyclization	en_US
dc.title	Photochemical rearrangement of calix[4]arene-derived bis(spirodienones): Formation of a new macrocycle	en_US
dc.type	Article	en_US
niist.citation