33553-22-9Relevant academic research and scientific papers
Tuneable access to indole, indolone, and cinnoline derivatives from a common 1,4-diketone Michael acceptor
Abdelli, Abderrahmen,Efrit, Mohamed Lotfi,El-Marrouki, Dalel,Gros, Philippe C.,M’Rabet, Hédi,Touchet, Sabrina
supporting information, p. 1722 - 1731 (2021/06/25)
A convergent strategy is reported for the construction of nitrogen-containing heterocycles from common substrates: 1,4-diketones and primary amines. Indeed, by just varying the substrates, the substituents, or the heating mode, it is possible to selectively synthesize indole, indolone (1,5,6,7-tetrahydroindol-4-one), or cinnoline (5,6,7,8-tetrahydrocinnoline) derivatives in moderate to excellent yields.
A NEW SYNTHESIS OF PHENYL KETONES BY INTRAMOLECULAR "DEOXYBENZOYLATION" OF ENOLS AND PHENOLS
Kay, I. Trevor,Glue, Stephen E. J.
, p. 113 - 116 (2007/10/02)
The phenylcyanocarbamoyl chloride 1 has been used as a benzoyl anion equivalent in an intramolecular process to effect the replacement of the hydroxyl group of enols and phenols by the benzoyl group.
