Incorporation of pyridazine rings in the structure of functionalized π-conjugated materials
S Achelle, N Ple, A Turck - RSC advances, 2011 - pubs.rsc.org
Throughout the past few decades, the development of new π-conjugated organic
compounds has received a lot of attention due to their potential applications ranging from …
compounds has received a lot of attention due to their potential applications ranging from …
Recent achievements in the chemistry of 1, 2-diazines
II Mangalagiu - Current Organic Chemistry, 2011 - ingentaconnect.com
Recent studies have centred on 1, 2-diazines derivatives, which proved to be invaluable
materials in the fields of medicine, opto-electronics and agriculture. 1, 2-diazines were found …
materials in the fields of medicine, opto-electronics and agriculture. 1, 2-diazines were found …
Efficient synthesis of indolizines and new imidazo [1, 2-a] pyridines via the expected cyclization of aromatic cycloimmonium ylides with electron deficient alkynes and …
C Sandeep, B Padmashali, RS Kulkarni - Tetrahedron Letters, 2013 - Elsevier
Aromatic cycloimmonium ylides underwent smooth cyclization with electron deficient
alkynes in presence of anhydrous K 2 CO 3 in DMF solvent at room temperature to afford …
alkynes in presence of anhydrous K 2 CO 3 in DMF solvent at room temperature to afford …
Pyrrolopyridazine derivatives as blue organic luminophores: synthesis and properties. Part 2
G Zbancioc, II Mangalagiu - Tetrahedron, 2010 - Elsevier
Two environmentally friendly methods, one in liquid and other in solid phase, for preparation
of highly fluorescent pyrrolopyridazine (PP) derivatives under microwave (MW) irradiation is …
of highly fluorescent pyrrolopyridazine (PP) derivatives under microwave (MW) irradiation is …
Pyrrolodiazine derivatives as blue organic luminophores: Synthesis and properties. Part 3
GN Zbancioc, T Huhn, U Groth, C Deleanu… - Tetrahedron, 2010 - Elsevier
A fast, efficient, general and environmentally friendly method for preparation of highly
fluorescent derivatives containing the pyrrolodiazine moiety using microwave (MW) …
fluorescent derivatives containing the pyrrolodiazine moiety using microwave (MW) …
Conformational effects on the lowest excited states of benzoyl-pyrrolopyridazine: Insights from PCM time-dependent DFT
Time-dependent density functional theory (TD-DFT) computations and steady-state
electronic spectroscopy measurements are performed on two recently synthesized …
electronic spectroscopy measurements are performed on two recently synthesized …
A novel approach for the synthesis of N-arylpyrroles
F Dumitrascu, E Georgescu, MR Caira, F Georgescu… - Synlett, 2009 - thieme-connect.com
Abstract Treatment of quinazolin-4 (3H)-one bromides with acetylenic dipolarophiles in 1, 2-
epoxybutane medium gave, in good yields, N-arylpyrroles instead of the corresponding …
epoxybutane medium gave, in good yields, N-arylpyrroles instead of the corresponding …
[HTML][HTML] Synthesis and fluorescence of new 3-biphenylpyrrolo [1, 2-c] pyrimidines
ML Tatu, E Georgescu, C Boscornea, MM Popa… - Arabian Journal of …, 2017 - Elsevier
Abstract New pyrrolo [1, 2-c] pyrimidines derivates having a biphenyl moiety at position 3
have been synthesized by 1, 3-dipolar cycloaddition of their corresponding N-ylides with …
have been synthesized by 1, 3-dipolar cycloaddition of their corresponding N-ylides with …
Coumarin substituted pyrrolo-fused heterocyclic systems by 1, 3-dipolar cycloadditon reactions
MM Popa, E Georgescu, C Draghici… - Monatshefte für Chemie …, 2015 - Springer
A variety of new pyrrolo-fused heterocyclic systems bearing a 3-carbonylchromen-2-one
moiety on the pyrrole rings was obtained based on 1, 3-dipolar cycloaddition reactions of …
moiety on the pyrrole rings was obtained based on 1, 3-dipolar cycloaddition reactions of …
Synthesis, ABTS-Radical Scavenging Activity, and Antiproliferative and Molecular Docking Studies of Novel Pyrrolo[1,2-a]quinoline Derivatives
C Nanjappa, SKT Hanumanthappa… - Synthetic …, 2015 - Taylor & Francis
Abstract A new 2, 2′-azinobis-(3-ethylbenzothiazoline-6-sulfonic acid)(ABTS)-radical
scavenging and antiproliferative agents of pyrrolo [1, 2-a] quinoline derivatives have been …
scavenging and antiproliferative agents of pyrrolo [1, 2-a] quinoline derivatives have been …