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A facile one-pot regioselective synthesis of functionalized novel benzo[f] chromeno[4,3-b][1,7]naphthyridines and benzo[f][1,7]naphthyridines via an imino Diels-Alder reaction

Authors
Arepalli, Sateesh KumarPark, ByeongwooJung, Jae-KyungLee, KihoLee, Heesoon
Issue Date
1-Feb-2017
Publisher
PERGAMON-ELSEVIER SCIENCE LTD
Keywords
13H-Benzo[f]chromeno[4,3-b]; [1,7]naphthyridines; 1,3-Diphenylbenzo[f][1,7]naphthyridines; Imino Diels-Alder reaction; Atom economy; One-pot multicomponent reaction
Citation
TETRAHEDRON LETTERS, v.58, no.5, pp.449 - 454
Indexed
SCIE
SCOPUS
Journal Title
TETRAHEDRON LETTERS
Volume
58
Number
5
Start Page
449
End Page
454
URI
https://scholar.korea.ac.kr/handle/2021.sw.korea/84498
DOI
10.1016/j.tetlet.2016.12.050
ISSN
0040-4039
Abstract
A novel series of functionalized 13H-benzo[f]chromeno[4,3-b][1,7]naphthyridines and 1,3-diphenylA-benzo[f][1,7]naphthyridines have been synthesized by an efficient regioselective one -pot multicomponent synthesis through intra and intermolecular imino Diels-Alder reaction. In this method, we have achieved complete regioselectivity and atom economy with polysubstituted core motifs in moderate to good yields. The proposed mechanism of this reaction has also discussed. (C) 2016 Elsevier Ltd. All rights reserved.
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