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perimidine

Known as: 1H-perimidine, peri-naphthimidazole 
National Institutes of Health

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Broader (1)

Quinazolines

Papers overview

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2018
2018
Perimidine-based synthetic receptors for determination of copper(II) in water solution
Abstract Perimidine-based chelators 1 and 2 were prepared, and their structures were confirmed by 1H and 13C NMR, MS spectroscopy… 
2017
2017
Cu(OAc)2-Catalyzed Aerobic Oxidative Dehydrogenation Coupling: Synthesis of Heptacyclic Quinolizino[3,4,5,6-kla]perimidines.
A Cu(OAc)2-catalyzed domino tricyclization between naphthalene-1,8-diamine and 2-(phenylethynyl)benzaldehyde is described… 
2014
2014
Crystal structure of (E)-2-(4-methoxystyryl)-2,3-dihydro-1H-perimidine acetonitrile monosolvate
The title compound, C20H18N2O·CH3CN, a perimidine derivative, crystallized as an acetonitrile monosolvate. The planes of the… 
2013
2013
2,2-Dimethyl-2,3-dihydro-1H-perimidine
The title compound, C13H14N2, was obtained from reaction of diaminonaphthalene with acetone. In both independent molecules in the… 
2013
2013
Naphthalene-1,8-diamine–2-(pyrimidin-2-yl)-1H-perimidine (2/1)
In the title adduct, C15H10N4·2C10H10N2, the pyrimidine ring is nearly co-planar with the heteroatomic perimidine ring, as… 
2011
2011
Synthesis and structure of 2-pyransoylperimidines.
2008
2008
Cytotoxic Effects of Some Perimidine Derivatives on F2408 and 5Rp7 Cell Lines
Summary In this study twenty perimidine derivatives were prepared in order to seek their cytotoxic and antiproliferative effects… 
2007
2007
Modulation of unconventional fluorescence of novel photochromic perimidine spirodimers.
Fluorescence modulation by a class of photochromic perimidine spirodimers, which exhibit a characteristic fluorescence associated… 
Highly Cited
2006
Highly Cited
2006
N-salicylideneanilines: tautomers for formation of hydrogen-bonded capsules, clefts, and chains.
[structure: see text] The synthesis, characterization, and solid-state structures of new salicylaldimines are reported. Bis(N… 
1976
1976
Vinyl derivatives of perimidine
In distinction from the procedure of [6], the condensation of the starting 1,2-dimethylperimidine with aromatic or heterocyclic… 
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