Pyrrolidine and iodine catalyzed domino aldol-Michael-dehydrogenative synthesis of flavones

Naik, Mayuri M.; Tilve, S.G.; Kamat, V.P.

dc.contributor.author	Naik, Mayuri M.
dc.contributor.author	Tilve, S.G.
dc.contributor.author	Kamat, V.P.
dc.date.accessioned	2015-06-04T04:22:27Z
dc.date.available	2015-06-04T04:22:27Z
dc.date.issued	2014
dc.identifier.citation	Tetrahedron Letters. 55(22); 2014; 3340-3343.	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2014.04.051
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/3058
dc.description.abstract	A one pot synthesis of flavones is established from 2'-hydroxyacetophenones and substituted aromatic aldehydes. The method uses domino aldol-Michael-oxidation reaction catalyzed by pyrrolidine as a base and iodine as an oxidant in dimethyl sulfoxide.	en_US
dc.publisher	Elsevier	en_US
dc.subject	Chemistry	en_US
dc.title	Pyrrolidine and iodine catalyzed domino aldol-Michael-dehydrogenative synthesis of flavones	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y