A rapid assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig Diels-Alder Reaction

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

dc.contributor.author	Torney, P.S.
dc.contributor.author	Patre, R.E.
dc.contributor.author	Tilve, S.G.
dc.date.accessioned	2015-06-04T03:08:12Z
dc.date.available	2015-06-04T03:08:12Z
dc.date.issued	2011
dc.identifier.citation	Synlett. (5); 2011; 639-642.	en_US
dc.identifier.uri	http://dx.doi.org/10.1055/s-0030-1259695
dc.identifier.uri	http://irgu.unigoa.ac.in/drs/handle/unigoa/2561
dc.description.abstract	Regioisomeric hexahydrofuro[3,4-b]carbazol-1-ones, hexahydropyrrolo[3,4-b] carbazol-1-ones, hexahydrofuro[3,4-b]carbazol-3-ones and hexahydropyrrolo[3,4-b] carbazol-3-ones were synthesized in 59 percent to 62 percent yields by domino Wittig Diels-Alder reactions from indole-3-carboxaldehyde and indole-2-carboxaldehyde and Wittig reagents. Further the corresponding carbazolelactones and carbazolelactams were obtained by oxidation with DDQ.	en_US
dc.publisher	Thieme Publishing	en_US
dc.subject	Chemistry	en_US
dc.title	A rapid assembly of Furo[3,4-b]- and Pyrrolo[3,4-b]carbazolones by Domino Wittig Diels-Alder Reaction	en_US
dc.type	Journal article	en_US
dc.identifier.impf	y