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A nickel catalyzed acceptorless dehydrogenative approach to quinolines†
Seuli Parua,Rina Sikari,Suman Sinha,Siuli Das,Gargi Chakraborty,Nanda D. Paul
Organic & Biomolecular Chemistry Pub Date : 12/05/2017 00:00:00 , DOI:10.1039/C7OB02670F
Abstract

A general, efficient and environmentally benign, one-step synthesis of substituted quinoline derivatives was achieved by acceptorless dehydrogenative coupling of o-aminobenzylalcohols with ketones and secondary alcohols catalyzed by a cheap, earth abundant and easy to prepare nickel catalyst [Ni(MeTAA)], featuring a tetraaza macrocyclic ligand (tetramethyltetraaza[14]annulene (MeTAA)). A wide variety of substituted quinolines were synthesized in high yields starting from readily available o-aminobenzylalcohols and ketones or secondary alcohols. A few controlled reactions were carried out to establish the acceptorless dehydrogenative nature of the reactions.

Graphical abstract: A nickel catalyzed acceptorless dehydrogenative approach to quinolines
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