Regioselective Olefination of 3‐Substituted Five‐Membered Heteroarenes

Five‐membered heteroarenes constitute ubiquitous moieties in bioactive compounds and materials. It is thus not surprising that a direct and selective access to multiply substituted heteroarenes is considered as a highly attractive synthetic target. The direct olefination of such substrates, also known as cross‐dehydrogenative coupling has raised significant interest in this context. However, achieving site‐selectivity remains challenging with some substitution patterns such as 3‐substituted heteroarenes. Suitable catalyst systems and reaction conditions have to be identified, which enable the differentiation between the competing C2‐ and C5‐position. Over the last few years, substantial progress has been made to overcome this selectivity challenge mainly based on the use of novel ligand systems, which will be described herein.

Location
Deutsche Nationalbibliothek Frankfurt am Main
Extent
Online-Ressource
Language
Englisch

Bibliographic citation
Regioselective Olefination of 3‐Substituted Five‐Membered Heteroarenes ; volume:2020 ; number:40 ; year:2020 ; pages:6318-6327 ; extent:10
European journal of organic chemistry ; 2020, Heft 40 (2020), 6318-6327 (gesamt 10)

Creator

DOI
10.1002/ejoc.202000659
URN
urn:nbn:de:101:1-2022062411130698766406
Rights
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
Last update
15.08.2025, 7:27 AM CEST

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