Synthesis of the naturally occurring prenylated coumarins balsamiferone and cedrelopsin by domino reactions

Patre, R.E.; Parameswaran, P.S.; Tilve, S.G.

dc.contributor.author	Patre, R.E.
dc.contributor.author	Parameswaran, P.S.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T03:06:42Z
dc.date.available	2015-06-04T03:06:42Z
dc.date.issued	2011
dc.identifier.citation	Arkivoc. 9; 2011; 68-76.	en_US
dc.identifier.uri	http://www.arkat-usa.org/get-file/39013/
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2556
dc.description.abstract	Regioselective one step synthesis of naturally occurring prenyl coumann balsamiferone is described using domino Wittig reaction, 3,3-sigmatropic rearrangements and deprenylation, while regioselective synthesis of cedrelopsin is described via domino Wittig reaction, prenylation and deprenylation.	en_US
dc.publisher	Michigan Publishing	en_US
dc.subject	Chemistry	en_US
dc.title	Synthesis of the naturally occurring prenylated coumarins balsamiferone and cedrelopsin by domino reactions	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y