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A nickel catalyzed acceptorless dehydrogenative approach to quinolines
Parua Seuli, Sikari Rina, Sinha Suman, Das Siuli, , Paul D. Nanda
Published in
2018
Volume: 16
   
Issue: 2
Pages: 274 - 284
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.
About the journal
JournalOrganic and Biomolecular Chemistry
ISSN14770520
Open AccessNo