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   <subfield code="a">The Behavior of Phosphorus Reagents Towards Substituted Diazine and Hydrazine Derivatives</subfield>
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   <subfield code="c">[Mona H. N. Arsanious, Leila S. Boulos]</subfield>
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   <subfield code="a">Summary.: The reaction of dibenzoyldiazine with phosphorus ylides afforded the new 2-[(benzoylhydrazono)phenylalkyl]but-2-enedioic acid dialkylesters. Moreover, ethyl-2(triphenylphosphoranylidene)propionate reacts with dibenzoyldiazine to give the olefinic compound and triphenylphosphine oxide. On the other hand, oxovinylidene-triphenylphosphorane reacts with dibenzoyldiazine to give a new phosphorane adduct. Trialkyl phosphites react with dibenzoyldiazine to yield the dialkyl phosphonate products. The reaction of dibenzoylhydrazide with Wittig reagents gave rise to the new 3,7-diphenylpyrazolo[1,2-α]pyrazole-1,5-diones. Possible reaction mechanisms are considered, and the structural assignments are based on analytical and spectroscopic results.</subfield>
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   <subfield code="a">Keywords. Ylides</subfield>
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   <subfield code="a">Trialkyl phosphites</subfield>
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   <subfield code="a">Diazines</subfield>
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   <subfield code="t">Monatshefte für Chemie / Chemical Monthly</subfield>
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