Heterocyclic compounds based on the [2.2] paracyclophane substructure have been known
since the 1960s, but there has been an upsurge of interest in the past few years. The …

Two cascade reactions have been developed for the time-efficient preparation of a variety of
functionalized aromatic heterocyclic products exhibiting an isoquinoline core. The approach …

Two tandem processes involving the cycloaddition of benzynes have been developed for
the synthesis of polyaromatic hydrocarbons. Benzynes react with fluorene-derived alkenes …

With 2-(trimethylsilyl) aryl triflates as aryne precursors, an unprecedented three-component
carboarylation reaction of unactivated imines with arynes and carbon nucleophiles has been …

Pseudo-three-component reactions are described for the conversion of simple N-aryl imines
into 1, 2-dihydroisoquinoline-type products. The approach relies on a regioselective …

The transition-metal-free multicomponent coupling of arynes, anilines, and ethylglyoxylate,
proceeding via an inverse electron-demand aza Diels–Alder cycloaddition and N-arylation …

Two pseudo-para substituted bis-diimino [2.2] paracyclophane ligands (4, 16-bis
(picolinaldimine)-[2.2] paracyclophane (BPPc) and 4, 16-bis (methyl-picolinaldimine)-[2.2] …

5-Benzyl-1H-tetrazols from the reaction of 1-aryl-5-methyl-1H-tetrazoles with 1,2-dehydrobenzene
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Les diarylazines réagissent avec le 1, 2-dihydrobenzène (o-benzyne) pour conduire à la
formation des 10-amino-9 (10 H)-acridones substituées en position 3. Par ailleurs, le 1, 1, 2 …

A PVC membrane of azomethine of piperonylidine-4-[2.2] paracyclophanylamine reveals a
Nernstian potentiometric response (with slope of 19.3±0.3 mV/decade) for Ce (III) over a …