A Concise Construction of Polycyclic Quinolines via Annulation of ω-Cyano-1-alkynes with Diaryliodonium Salts
Organic Letters2013Vol. 15(18), pp. 4794–4797
Citations Over TimeTop 10% of 2013 papers
Abstract
A concise construction of polycyclic quinolines via intramolecular [2 + 2 + 2] annulation of ω-cyano-1-alkynes with diaryliodonium salts was realized. The process produced polycyclic quinolines in high yields with readily available staring materials and was tolerated with halogen substituents.
Related Papers
- → Synthesis of Natural Products, Carbocycles, and Heterocycles by Hauser–Kraus Annulation(2023)13 cited
- → [3 + 2] Annulation of Allylidenetriphenylphosphorane with 1,2-Diacylethylenes and 1,2-Diacylacetylenes: A One-Step Synthesis of Tri- and Tetrasubstituted Cyclopentadienes and Fulvenes(1997)38 cited
- → π-Conjugated carbocycles and heterocycles via annulation through C-H and X-Y activation across CC triple bonds(2015)4 cited
- → [4 + 2] Annulation of Activated o-Toluate/o-Tolualdehyde Donors (Hauser-Leusen Annulation)(2018)1 cited
- → [4 + 2] Annulation With Nonactivated o-Toluate Donors (Staunton-Weinreb-Myers Annulation)(2018)