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Synthesis of novel 2-aryl-3-benzoyl-1H-benzo[f]indole-4,9-diones using a domino reaction

Nguyen, T.Q. and Le Nhat, T.G. and Vu Ngoc, D. and Dang Thi, T.A. and Nguyen, H.T. and Hoang Thi, P. and Nguyen, H.H. and Cao, H.T. and Abbaspour Tehrani, K. and Nguyen, T.V. (2016) Synthesis of novel 2-aryl-3-benzoyl-1H-benzo[f]indole-4,9-diones using a domino reaction. Tetrahedron Letters, 57 (39). pp. 4352-4355. ISSN 404039

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Abstract

A convenient one-pot multicomponent synthetic approach was developed for the synthesis of novel 2-aryl-3-benzoyl-1H-benzo[f]indole-4,9-diones using 2-amino-1,4-naphthoquinone, N-acylmethylpyridinium bromides, and a variety of aromatic aldehydes. © 2016 Elsevier Ltd

Item Type: Article
Divisions: Faculties > Faculty of Physical and Chemical Engineering
Identification Number: 10.1016/j.tetlet.2016.08.042
Uncontrolled Keywords: 1,4 naphthoquinone; aldehyde derivative; bromine derivative; indole derivative; pyridinium derivative; Article; biological activity; carbon nuclear magnetic resonance; catalyst; chemical reaction; column chromatography; cyclization; domino reaction; Knoevenagel condensation; Michael addition; nucleophilicity; one pot synthesis; proton nuclear magnetic resonance; purification; structure activity relation; tautomerization; X ray analysis
Additional Information: Language of original document: English. All Open Access, Green.
URI: http://eprints.lqdtu.edu.vn/id/eprint/9872

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