A nitrogen-ligated nickel-catalyst enables selective intermolecular cyclisation of β- and γ-amino alcohols with ketones: access to five and six-membered N-heterocycles. Issue 10 (23rd April 2018)

• Record Type: Journal Article
• Authors: Singh, Khushboo; Vellakkaran, Mari; Banerjee, Debasis
• Is Part Of: Green chemistry. Volume 20:Issue 10(2018)
• Page Start: 2250
• Page End: 2256
• Publication Date: 2018-04-23
• Subjects: Environmental chemistry -- Industrial applications -- Periodicals; Environmental management -- Periodicals; 660
• DOI: 10.1039/c8gc00318a
• Languages: English
• ISSNs: 1463-9262

Abstract

Abstract : Nickel-catalysed conversion of β- and γ-amino alcohols with ketones enables selective construction of pyrroles, pyridines and quinolines by liberation of hydrogen gas and water as sole by-products. Abstract : Owing to the great demand for the synthesis of N-heterocycles, development of new reactions that utilise renewable resources and convert them into key chemicals using non-precious base metal-catalysts is highly desirable. Herein, we demonstrated a sustainable Ni-catalysed dehydrogenative approach for the synthesis of pyrroles, pyridines, and quinolines by the reaction of β- and γ-amino alcohols with ketones via C–N and C–C bond formations in a tandem fashion. A variety of aryl, hetero-aryl, and alkyl ketones having free amine, halide, alkyl, alkoxy, alkene, activated benzyl, and pyridine moieties were converted into synthetically interesting 2, 3 and 2, 3, 5-substituted bicyclic as well as tricyclic N-heterocycles with up to 90% yields. As a highlight, we demonstrated the synthesis of an interesting pyrrole derivative by intermolecular cyclisation of a steroid hormone with phenylalaninol.