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DMSO-assisted environmentally benign synthesis of benzo[ c ]-chromeno[4,3,2- gh ]phenanthridines by remote oxidative hetero cross-coupling cyclization and aromatization reaction.

Sabina YashminRashid AliSanta MondalAbu Taleb Khan
Published in: Chemical communications (Cambridge, England) (2022)
An unprecedented metal-free and catalyst-free synthesis of benzo[ c ]chromeno[4,3,2- gh ]phenanthridine derivatives, a class of 1,6-diheterophenalenoid heterocycle, is reported for the first time. The oxidative cross-coupling reaction for the remote cyclization is achieved through the in situ generated o -quinone methide intermediate followed by an electrocyclic ring closure reaction. The aromatization of the cyclohexane ring is achieved by sequential H shift, hydroxylation, and elimination reaction. DMSO-assisted concomitant cyclization and aromatization reactions are also disclosed for the first time.
Keyphrases
  • growth hormone
  • ionic liquid
  • reduced graphene oxide