Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
5278920 | Tetrahedron Letters | 2011 | 5 Pages |
Abstract
A convenient and efficient procedure for the synthesis of 4-arylchromenes, thiochromenes, and related heterocycles via a four step-sequence has been developed. The first three steps, which involve hydration of alkynes, hydrazones formation, and their Pd-coupling with ortho substituted aryl halides, furnished stereoselectively Z-trisubstituted olefins without any purification of the intermediates generated in each stage. These latter proved to be suitable precursors, in the last step, for the synthesis of the desired heterocycles of biological interest.
Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Evelia Rasolofonjatovo, Bret Tréguier, Olivier Provot, Abdallah Hamze, Estelle Morvan, Jean-Daniel Brion, Mouad Alami,