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First syntheses of two quinoline alkaloids from the medicinal herb Ruta Chalepensisvia cyclization of an o-iodoaniline with an acetylenic sulfone†
Thomas G. Back,Jeremy E. Wulff
Chemical Communications Pub Date : 07/08/2002 00:00:00 , DOI:10.1039/B205408F
Abstract

The first syntheses of two quinoline alkaloids found in the medicinal herb Ruta chalepensis are reported via the conjugate addition of an o-iodoaniline to an acetylenic sulfone, followed by Pd-catalyzed carbonylation, intramolecular acylation of the coresponding sulfone-stabilized carbanion, and reductive desulfonylation.

Graphical abstract: First syntheses of two quinoline alkaloids from the medicinal herb Ruta Chalepensisvia cyclization of an o-iodoaniline with an acetylenic sulfone
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