Synlett
DOI: 10.1055/a-2738-8420
Account

Selective Construction of Diverse Polycyclic Compounds by Electrophilic Cyclizations of Biaryl-Embedded 1,7-Enynes

Authors

  • Lucía Sánchez-Jiménez

    1   Instituto de Investigación Química “Andrés M. del Río” (IQAR), Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, Alcalá de Henares, Spain (Ringgold ID: RIN16720)
  • Patricia García-García

    1   Instituto de Investigación Química “Andrés M. del Río” (IQAR), Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, Alcalá de Henares, Spain (Ringgold ID: RIN16720)
  • Manuel Á. Fernández-Rodríguez

    1   Instituto de Investigación Química “Andrés M. del Río” (IQAR), Departamento de Química Orgánica y Química Inorgánica, Universidad de Alcalá, Alcalá de Henares, Spain (Ringgold ID: RIN16720)

Supported by: Instituto de Salud Carlos III RICORS2040 (RD24/0004/0008)
Supported by: Universidad de Alcalá predoctoral contract for L.S.-J.
We are grateful to MCIN/AEI/10.13039/501100011033 and European Union NextGeneration EU/PRTR for grant PID2023-146343NB-I00, to Instituto de Salud Carlos III (ISCIII) for grant RICORS2040 (RD24/0004/0008) co-funded by the European Union and to the University of Alcalá (predoctoral contract for L.S.-J.).


Graphical Abstract

Abstract

Electrophilic cyclizations of biaryl-embedded 1,7-enynes enable the selective synthesis of dibenzofused polycycles with diverse topologies. The outcome strongly depends on the promoter—gold(I) complexes, Brønsted acids, or electrophilic boron reagents—as well as the substitution pattern of the enyne. This Account highlights recent advances and establishes a basis for future developments through the controlled design of substrates and activation modes.



Publication History

Received: 30 September 2025

Accepted after revision: 04 November 2025

Article published online:
18 November 2025

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