Synthesis of heterocyclic compounds through nucleophilic phosphine catalysis
Chemical Communications2020Vol. 56(97), pp. 15235–15281
Citations Over TimeTop 10% of 2020 papers
Abstract
Nucleophilic phosphine catalysis is a practical and powerful tool for the synthesis of various heterocyclic compounds with the advantages of environmentally friendly, metal-free, and mild reaction conditions. The present report summarizes the construction of four to eight-membered heterocyclic compounds containing nitrogen, oxygen and sulphur atoms through phosphine-catalyzed intramolecular annulations and intermolecular [2+2], [3+2], [4+1], [3+1+1], [5+1], [4+2], [2+2+2], [3+3], [4+3] and [3+2+3] annulations of electron-deficient alkenes, allenes, alkynes and Morita-Baylis-Hillman carbonates.
Related Papers
- → Comprehensive Study of the Reactions Between Chelating Phosphines and Ni(cod)2(2018)41 cited
- → 31P NMR studies of cis-[RhCl(CO)(bis-phosphine)] complexes(1987)14 cited
- → Reaction of secondary phosphine chalcogenides with diallylamine(2014)2 cited
- Phosphine oxides, sulphides, selenides and tellurides(1992)
- → Nucleophilic Additions to Alkynes and Reactions via Vinylidene Intermediates(2004)19 cited