2014
DOI: 10.1002/jhet.1821
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Recent Heterocyclic Compounds from (1,3‐Dioxo‐2,3‐dihydro‐1H‐inden‐2‐ylidene)propanedinitrile

Abstract: This review summarizes the literatures dealing with the synthesis of some important nitrogen or nitrogen/sulfur heterocyclic, spiroheterocyclic, and fused heterocyclic compounds.

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Cited by 2 publications
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“…The mechanism was described as due to nucleophilic attacked of 54a–d , j to the C═C double bond of 44 followed by elimination of a molecule of malononitrile to form first intermediate 203a–e (Scheme ). Then intramolecular nucleophilic attack of NH to the carbonyl group to give second intermediate 204a–e was followed by elimination of H 2 O to provide thioxoindenotriazines 205a–e (Scheme ) .…”
Section: Thiosemicarbazidesmentioning
confidence: 99%
“…The mechanism was described as due to nucleophilic attacked of 54a–d , j to the C═C double bond of 44 followed by elimination of a molecule of malononitrile to form first intermediate 203a–e (Scheme ). Then intramolecular nucleophilic attack of NH to the carbonyl group to give second intermediate 204a–e was followed by elimination of H 2 O to provide thioxoindenotriazines 205a–e (Scheme ) .…”
Section: Thiosemicarbazidesmentioning
confidence: 99%