The Intramolecular Cycloadditon Reaction of N'-Alkyl-N3-[[(2-cyanophenyl)imino](phenyl)methyl]thioureas
Authors | |
---|---|
Year of publication | 2001 |
Type | Article in Proceedings |
Conference | Sborník príspevkov 53. zjazd Chemických spoločností |
MU Faculty or unit | |
Citation | |
Field | Organic chemistry |
Keywords | Quinazolines; thioureas; domino-reactions |
Description | The intramolecular cycloaddition reaction of N1-R- or N1,N1-Di-R-N3-[[(2-cyanophenyl)imino](phenyl)-methyl]thioureas formed in situ by addition of amines to N2-(2-cyanophenyl)-N1-thioxo-methylidenebenzene-1-carboximidamide 1 were investigated. These thioureas undergo cyclization folowed by Dimroth rearrangement and quinazolin-4-yl or quinazolin-4-ylidene thioureas were identified. |
Related projects: |