| Literature DB >> 21301938 |
Raghunath B Toche1, Ravindra A Janrao, Sandeep M Bagul, Shivaraj P Patil, Balasaheb P Pagar, Prashant S Nikam.
Abstract
Suzuki-Miyaura cross coupling was successfully used for C5-arylation in 4-amino-2-chloroquinoline-3-carbaldehyde using arylbornic acid and tetrakistriphenylphosphine palladium catalyst in water. Friedländer condensation reaction on 4-amino-2-chloro/2-arylquinoline-3-carbaldehyde and aromatic ketones gave novel aryl and diarylbenzo[h] [1, 6]naphthyridines in good yields. Fluorescence quantum yields were increased by introducing C2 and C5 π donor aryl benzo[h][1, 6]naphthyridines derivatives. © Springer Science+Business Media, LLC 2011Entities:
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Year: 2011 PMID: 21301938 DOI: 10.1007/s10895-011-0850-2
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217