The first chemo- and regiospecific palladium-catalyzed enyne-diyne [4+2] intermolecular cross-benzannulation: an effective route to polysubstituted benzenes
- 8 December 1997
- journal article
- Published by Elsevier in Tetrahedron Letters
- Vol. 38 (49) , 8603-8604
- https://doi.org/10.1016/s0040-4039(97)10295-7
Abstract
No abstract availableThis publication has 3 references indexed in Scilit:
- A New Palladium-Catalyzed Benzannulation of Conjugated EnynesJournal of the American Chemical Society, 1996
- Strained Cyclic Cumulene Intermediates in Diels−Alder Cycloadditions of Enynes and DiynesJournal of the American Chemical Society, 1996
- Intramolecular [4+2] Cycloaddition Reactions of Conjugated EnynesThe Journal of Organic Chemistry, 1994