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   <subfield code="a">Synthesis of 2-hetaryl-2-(tetrahydrofuran-2-ylidene)acetonitriles</subfield>
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   <subfield code="c">[O. Khilya, T. Volovnenko, A. Turov, R. Zubatyuk, O. Shishkin, Yu. Volovenko]</subfield>
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   <subfield code="a">The reaction of azolylacetonitriles with γ-chlorobutyryl chlorides gave the corresponding 2-(1-R-1,3-di- hydro-2H-benzimidazol-2-ylidene)-, 2-(1,3-benzothiazol-2-ylidene)-, and 6-chloro-2-(4-methylthiazol-2-ylidene)-3-oxohexanenitriles. A study of the intramolecular cyclization of 2-(quinazolin-2-ylidene)-3-oxo-6-hexanenitriles and -heptanenitriles has led to the development of an efficient method for the preparation of 2-(quinazolin-2-yl)-2-(tetrahydrofuran-2-ylidene)acetonitriles. The (Z,E)-isomerism of the synthesized 2-hetaryl-2-(tetrahydrofuran-2-ylidene)acetonitriles was studied.</subfield>
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