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Arylidene Derivatives as Synthons in Heterocyclic Synthesis

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DOI: 10.4236/oalib.1100367    2,929 Downloads   4,931 Views   Citations
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ABSTRACT

This review describes the synthetic procedures for the preparation of arylideneacetophenones, arylidenecycloalkanones, 2-arylidene-1-indanones, 2-arylidene-1-tetralones, 2-arylidene-1-benzosuberones, aurones, 1-thioaurones, 3-arylidene-4-chromanones, 3-arylidene-1-thio-4-chromanones, 3-arylideneflavanones, 3-arylidene-1-thioflavanones, arylideneanilines, arylidenemalononitriles, diethylarylidenemalonates, ethylarylidenecyanoacetates, arylidenecyanoacetamides, 5-arylidene derivatives of barbituric and thiobarbituric acids, arylidene derivatives of Meldrum’s acid and arylidene derivatives of dimedone. Also, it demonstrates the reactivity of these arylidene derivatives in heterocyclic synthesis with emphasis on the most recent findings. Some of these are the α,β-enones, víz. aurones and 3-arylidene-4-chromanones belong to the natural products. The others are synthetic substances which are convenient and important intermediates for the synthesis of a variety of useful and novel heterocyclic systems.

Conflicts of Interest

The authors declare no conflicts of interest.

Cite this paper

El-Gohary, N. (2014) Arylidene Derivatives as Synthons in Heterocyclic Synthesis. Open Access Library Journal, 1, 1-47. doi: 10.4236/oalib.1100367.

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