FeCl3 promoted cycloisomerization of 1,6-dienes

Release time:2025-02-04 Hits:

DOI number:10.1039/d4qo02201g

Journal:Org. Chem. Front.

Abstract:A highly selective cycloisomerization of 1,6-dienes by FeCl3 catalysis has been developed. Both symmetric and unsymmetric dienes could undergo this cycloisomerization through a carbocation pathway activated by Lewis acid FeCl3. This protocol offers a green approach to access α-alkenyl-tetrahydropyridine compounds with high yields and good selectivity.

Indexed by:Journal paper

Translation or Not:no

Date of Publication:2025-02-04

Included Journals:SCI

Links to published journals:https://pubs.rsc.org/en/content/articlepdf/2025/qo/d4qo02201g