1131341-99-5Relevant academic research and scientific papers
Domino rhodium(I)-catalysed reactions for the efficient synthesis of substituted benzofurans and indoles
Boyer, Alistair,Isono, Naohiro,Lackner, Sebastian,Lautens, Mark
experimental part, p. 6468 - 6482 (2010/10/03)
Rhodium(I) catalysts promote the transformation of o-alkynyl phenols and anilines to the corresponding benzo[b]furans and indoles. The reaction is postulated to proceed via a transient 3-rhodium heterocycle intermediate, which can be trapped with suitable electrophiles to give poly-substituted heterocycles. In the case of mono-substituted electron-withdrawn electrophiles, excellent yield and selectivity for conjugate addition versus Heck-Mizoroki reaction can be achieved. In the case of 2-alkynyl pyridine electrophiles, novel 2-(benzofuran-3-yl)vinylpyridines are formed.
Rhodium(I)-catalyzed cyclization reaction of o-alkynyl phenols and anilines. Domino approach to 2,3-disubstituted benzofurans and indoles
Isono, Naohiro,Lautens, Mark
supporting information; experimental part, p. 1329 - 1331 (2009/10/02)
A rhodium-catalyzed cyclization of o-alkynylphenols and anilines followed by intermolecular conjugate addition that succeeds with alkyl and aryl alkynes is reported. In this reaction, 2,3-disubstituted benzofurans or indoles are obtained in one pot in good to excellent yields.
