An efficient, rapid, and regioselective bromination of anilines and phenols with 1-butyl-3-methylpyridinium tribromide as a new reagent/solvent under mild conditions-Reference-Cited by-同舟云学术

An efficient, rapid, and regioselective bromination of anilines and phenols with 1-butyl-3-methylpyridinium tribromide as a new reagent/solvent under mild conditions

Published:2009-03 Issue:9 Volume:50 Page:1007-1009
ISSN:0040-4039
Container-title:Tetrahedron Letters
language:en
Short-container-title:Tetrahedron Letters

Author:

Borikar Sanjay P.,Daniel Thomas,Paul Vincent

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference34 articles.

1. Palladium-Catalyzed Tetrakis(dimethylamino)ethylene-Promoted Reductive Coupling of Aryl Halides

2. Ligand-Free Heck Reaction: Pd(OAc)2 as an Active Catalyst Revisited

3. A highly efficient catalytic system for cross-coupling of aryl chlorides and bromides with malononitrile anion by palladium carbene complexesElectronic supplementary information (ESI) available: experimental details. See http://www.rsc.org/suppdata/cc/b3/b302890a/

4. Monomeric (dialkylamino)boranes: a new and efficient boron source in palladium catalyzed C–B bond formation with aryl halides

5. Brominations with Pyridine Hydrobromide Perbromide

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