We found a match
Your institution may have rights to this item. Sign in to continue.
- Title
Suzuki-Miyaura Reactions of Halospirooxindole Derivatives.
- Authors
El Bouakher, Abderrahman; Allouchi, Hassan; Abrunhosa‐Thomas, Isabelle; Troin, Yves; Guillaumet, Gérald
- Abstract
Starting from 5,5′-dihalo-1′-pentyl-2 H-spiro[furo[2,3- b]pyridine-3,3′-indolin]-2′-one, various 5,5′-di(het)aryl-1′-pentyl-2 H-spiro[furo[2,3- b]pyridine-3,3′-indolin]-2′-ones were synthesized through palladium-catalysed cross-coupling reactions. A large panel of boronic acids (aryl or heteroaryl) could easily be introduced, leading to a library of new 5- or 5′-monosubstituted and 5,5′-disubstituted 1′-pentyl-2 H-spiro[furo[2,3- b]pyridine-3,3′-indolin]-2′-ones.
- Subjects
SUZUKI reaction; PALLADIUM; OXINDOLES; CATALYSIS synthesis; PYRIDINE
- Publication
European Journal of Organic Chemistry, 2015, Vol 2015, Issue 16, p3450
- ISSN
1434-193X
- Publication type
Article
- DOI
10.1002/ejoc.201500268