Domino Wittig Diels-Alder reaction: An expeditious entry into the AB ring system of furanosesquiterpenes
dc.contributor.author | Patre, R.E. | |
dc.contributor.author | Gawas, S. | |
dc.contributor.author | Sen, S. | |
dc.contributor.author | Parameswaran, P.S. | |
dc.contributor.author | Tilve, S.G. | |
dc.date.accessioned | 2008-01-30T12:41:27Z | |
dc.date.available | 2008-01-30T12:41:27Z | |
dc.date.issued | 2007 | |
dc.identifier.citation | Tetrahedron letters, Vol.48; 3517-3520p. | |
dc.identifier.uri | http://drs.nio.org/drs/handle/2264/668 | |
dc.description.abstract | A domino Wittig Diels - Alder reaction has been employed in delineating a short and flexible synthetic stratagem for ready access to the AB ring system and the tricyclic framework of furanosesquiterpenes, such as the bioactive natural products, furodysin and furodysinin. | |
dc.language.iso | en | |
dc.publisher | Elsevier | |
dc.subject | bioactive compounds | |
dc.subject | molecular structure | |
dc.subject | chemical reaction | |
dc.title | Domino Wittig Diels-Alder reaction: An expeditious entry into the AB ring system of furanosesquiterpenes | |
dc.type | Journal Article |
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