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Deconstructive annulation mediated one-pot synthesis of xanthene derivatives.

Balasubramaniyam ManikandanSubbiah ThamotharanOlivier BlacqueSubramaniapillai Selva Ganesan
Published in: Organic & biomolecular chemistry (2024)
Direct conversion of naphthoxazines to diverse xanthene derivatives was achieved under one-pot operation through deconstructive annulation methodology. Sequential oxidative C(sp 3 )-O/C(sp 3 )-N cleavage followed by intramolecular/intermolecular annulation reaction was carried out under aerobic reaction conditions. Mechanistic analyses performed on the substrate revealed that the C(sp 3 )-O bond cleavage supersedes the C(sp 3 )-N bond scission. The in situ generated Betti base intermediate through the C(sp 3 )-O cleavage was successfully isolated. Based on a molecular docking investigation, the intermolecular annulated products demonstrated good α-glucosidase inhibitory properties.
Keyphrases
  • molecular docking
  • dna binding
  • molecular dynamics simulations
  • energy transfer
  • structure activity relationship