A metal-free approach towards synthesis of β-carboline C1 substituted Pyrido(2,3-c)carbazole derivatives (nitramarine analogues) through A3-coupling and estimation of their light emitting properties

被引:10
|
作者
Singh, Manpreet [1 ]
Vaishali [1 ]
Kumar, Sunit [1 ]
Jamra, Rahul [1 ]
Pandey, Satyendra K. [2 ]
Singh, Virender [1 ,3 ]
机构
[1] Dr BR Ambedkar Natl Inst Technol NIT Jalandhar, Dept Chem, Jalandhar 144011, Punjab, India
[2] Banaras Hindu Univ, Dept Chem, Varanasi 221005, Uttar Pradesh, India
[3] Cent Univ Punjab, Dept Chem, Bathinda 151001, Punjab, India
关键词
Nitramarine; beta-Carboline; A3; coupling; Povarov; Quinoline; LAVENDAMYCIN METHYL-ESTER; BIOLOGICAL EVALUATION; PHOTOPHYSICAL PROPERTIES; IRIDIUM(III) COMPLEXES; REVERSE-TRANSCRIPTASE; ANTIMALARIAL ACTIVITY; STRUCTURAL DIVERSITY; HIGHLY EFFICIENT; ANTICANCER; QUINOLINE;
D O I
10.1016/j.tet.2020.131640
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A simple and efficient metal-free methodology is presented to access fluorescent beta-carboline tethered pyrido(2,3-c)carbazole derivatives (Nitramarine analogues) via A(3)-coupling of 1-formyl-9H-beta-carbolines, 3-amino-9-ethylcarbazole, and terminal alkynes. The advantages of this approach are operationally simple procedure, use of non-toxic and inexpensive catalyst (I-2), broad substrate scope, and good yields of products. Moreover, these products showed excellent luminescent properties with quantum yield (Phi(F)) up to 60%. (C) 2020 Elsevier Ltd. All rights reserved.
引用
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页数:12
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