From Simple Furans to Complex Nitrogen‐Bearing Aromatic Polycycles by Means of a Flexible and General Reaction Sequence Initiated by Singlet Oxygen
Open Access
- 14 June 2013
- journal article
- Published by Wiley in Chemistry – A European Journal
- Vol. 19 (31), 10119-10123
- https://doi.org/10.1002/chem.201301571
Abstract
A new and general one-pot reaction sequence initiated by singlet oxygen that transforms simple furan substrates into complex nitrogen-bearing aromatic polycycles having all the structural features of a number of important natural products is reported. The reaction sequence itself uses mild conditions and has wide functional group toleranceFunding Information
- European Research Council (277588)
This publication has 64 references indexed in Scilit:
- N-Acyliminium Cyclization as an Approach for an Asymmetric Synthesis of the Pyrrolo[2,1-a]benzazepine Ring SystemSynthetic Communications, 2011
- Cascade polycyclisations in natural product synthesisOrganic & Biomolecular Chemistry, 2011
- Kaskadenreaktionen in der TotalsyntheseAngewandte Chemie, 2006
- Cascade Reactions in Total SynthesisAngewandte Chemie, 2006
- Cyclizations of N-Acyliminium IonsChemical Reviews, 2004
- Stereoselective synthesis of the pyrroloisoquinoline ring systemTetrahedron Letters, 2001
- Domino Reactions in Organic SynthesisChemical Reviews, 1996
- The Pictet-Spengler condensation: a new direction for an old reactionChemical Reviews, 1995
- Intramolecular reactions of N-acyliminium intermediatesTetrahedron, 1985
- Über die Bildung von Isochinolin‐derivaten durch Einwirkung von Methylal auf Phenyl‐äthylamin, Phenyl‐alanin und TyrosinEuropean Journal of Inorganic Chemistry, 1911