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Acid-catalysed intramolecular Friedel-Crafts annulation of hetero-atom-functionalized para-quinone methides: access to O-, S- and N-based heterocycles.
Sharma, Sonam; Singh, Gurdeep; Kumar, Munnu; Vijaya Anand, Ramasamy.
Afiliación
  • Sharma S; Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S. A. S. Nagar, Manauli (PO), Punjab - 140306, India. rvijayan@iisermohali.ac.in.
  • Singh G; Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S. A. S. Nagar, Manauli (PO), Punjab - 140306, India. rvijayan@iisermohali.ac.in.
  • Rekha; Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S. A. S. Nagar, Manauli (PO), Punjab - 140306, India. rvijayan@iisermohali.ac.in.
  • Kumar M; Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S. A. S. Nagar, Manauli (PO), Punjab - 140306, India. rvijayan@iisermohali.ac.in.
  • Vijaya Anand R; Department of Chemical Sciences, Indian Institute of Science Education and Research (IISER) Mohali, Sector 81, S. A. S. Nagar, Manauli (PO), Punjab - 140306, India. rvijayan@iisermohali.ac.in.
Org Biomol Chem ; 21(24): 5072-5078, 2023 Jun 21.
Article en En | MEDLINE | ID: mdl-37273009
ABSTRACT
We describe here an acid-mediated one-pot approach to access substituted xanthene and thioxanthane derivatives from ortho-heteroaryl phenyl-substituted para-quinone methides via 1,6 intramolecular arylation. The scope of this work was further elaborated to the synthesis of 10H-indolo[1,2-a]indole-based heterocyclic systems using indole based para-quinone methides.

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: India

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Idioma: En Revista: Org Biomol Chem Asunto de la revista: BIOQUIMICA / QUIMICA Año: 2023 Tipo del documento: Article País de afiliación: India