Catalytic reductive N-alkylation of anilines. Application to the synthesis of N-aryl aminoacid precursors

Autor:	Fabienne Fache, F. Valot, Marc Lemaire, Alexandra Milenkovic
Přispěvatelé:	Institut de recherches sur la catalyse (IRC), Centre National de la Recherche Scientifique (CNRS), IRCELYON, ProductionsScientifiques
Jazyk:	angličtina
Rok vydání:	1996
Předmět:	010405 organic chemistry Chemistry Aryl Organic Chemistry [CHIM.CATA] Chemical Sciences/Catalysis [CHIM.CATA]Chemical Sciences/Catalysis Alkylation 010402 general chemistry 01 natural sciences Biochemistry 0104 chemical sciences Catalysis chemistry.chemical_compound Drug Discovery Organic chemistry
Zdroj:	Tetrahedron Tetrahedron, Elsevier, 1996, 52, pp.9777-9784
ISSN:	0040-4020
Popis:	different anilines have been monoalkylated by reductive alkylation using ketones and α-ketoesters as alkylating agents with good isolated yields. This provided access to aminoacid derivatives. Diastereoselective experiments were also performed.
Databáze:	OpenAIRE
Externí odkaz:	https://explore.openaire.eu/search/publication?articleId=doi_dedup___::39caaa30d50fe13ff37915900d3c2734 https://hal.archives-ouvertes.fr/hal-00006421 Zobrazit plný text záznamu Full Text from ScienceDirect