Palladium-Catalyzed Reactions on 1,2-Diazines

Bert U.W. Maes; Pal Tapolcsanyi; Caroline Meyers; Peter Matyus

doi:10.2174/138527206775473841

ISSN: 1385-2728
E-ISSN: 1875-5348

Palladium-Catalyzed Reactions on 1,2-Diazines
Authors: Bert U.W. Maes¹, Pal Tapolcsanyi², Caroline Meyers³ and Peter Matyus⁴
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¹ Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium. ² Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium. ³ Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium. ⁴ Department of Chemistry, University of Antwerp, Groenenborgerlaan 171, B-2020 Antwerp, Belgium.
Source: Current Organic Chemistry, Volume 10, Issue 3, Feb 2006, p. 377 - 417
DOI: https://doi.org/10.2174/138527206775473841
- Available online: 01 Feb 2006

Abstract

In this report, we review the C- and N-functionalization of the pyridazine nucleus via palladium-catalyzed reactions (Suzuki, Stille, Sonogashira, carbonylation, Heck, Buchwald-Hartwig) in which carbon atoms of the pyridazine nucleus are involved. The efficient use of these reactions in synthetic strategies to build up polycyclic 1,2-diazines is also included.

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2006-02-01

2025-05-19

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Article Type: Research Article

Keyword(s): brominated bicyclic fused system; Chloropyridazines; Negishi Reaction; Organometallic reagents; pyridazine nucleus

Palladium-Catalyzed Reactions on 1,2-Diazines

Abstract

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