Synthesis of 1,2-Dihydropyridines Catalyzed by Well-Defined Low-Valent Cobalt Complexes: C-H Activation Made Simple

Autor: Marc Petit, Jean-Baptiste Garsi, Etienne Derat, Brendan J. Fallon, Corinne Aubert, Muriel Amatore
Přispěvatelé: Méthodes et Application en Chimie Organique (MACO), Institut Parisien de Chimie Moléculaire (IPCM), Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Institut de Chimie du CNRS (INC)-Centre National de la Recherche Scientifique (CNRS), CNRS, MRES, UPMC, ANR [ANR-12-BS07-0031- 01COCACOLIGHT], Institut de Chimie du CNRS (INC)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)-Institut de Chimie du CNRS (INC)-Université Pierre et Marie Curie - Paris 6 (UPMC)-Centre National de la Recherche Scientifique (CNRS)
Jazyk: angličtina
Rok vydání: 2015
Předmět:
Zdroj: ACS Catalysis
ACS Catalysis, 2015, 5 (12), pp.7493-7497. ⟨10.1021/acscatal.5b02138⟩
ACS Catalysis, American Chemical Society, 2015, 5 (12), pp.7493-7497. ⟨10.1021/acscatal.5b02138⟩
ISSN: 2155-5435
DOI: 10.1021/acscatal.5b02138⟩
Popis: International audience; A convenient one-pot system has been developed, allowing the synthesis of highly substituted dihydropyridines via a C-H activation/6 pi-electrocyclization pathway. The reaction proceeds with high regioselectivity, and we disclose the first example of isolated dihydropyridines lacking substitution in the 2 position. Moreover, the use of a simple well-defined low-valent cobalt complex without the need for reducing agents or additives in combination with computational studies provides a clearer insight into the C-H activation pathway than was previously reported.
Databáze: OpenAIRE