Palladium-catalyzed N1-selective allylation of indoles with allylic alcohols promoted by titanium tetraisopropoxide. Issue 8 (9th January 2019)

• Record Type: Journal Article
• Authors: Chang, Chieh-Yu; Lin, Yu-Huan; Wu, Yen-Ku
• Is Part Of: Chemical communications. Volume 55:Issue 8(2019)
• Page Start: 1116
• Page End: 1119
• Publication Date: 2019-01-09
• Subjects: Chemistry -- Periodicals; 540
• DOI: 10.1039/c8cc09817d
• Languages: English
• ISSNs: 1359-7345

Abstract

Abstract : The N1-selective allylation of indoles with allylic alcohols has been accomplished by synergistic functions of palladium catalysts and titanium tetraisopropoxide. Abstract : The direct N1-selective allylation of indoles with allylic alcohols has been accomplished by synergistic functions of palladium catalysts and titanium tetraisopropoxide. The site selectivity is notably different from that observed in other related transition metal-catalyzed approaches. This chemistry provides a facile route to a variety of allylated indoles in synthetically useful yields. The utility of this simple allylation reaction was demonstrated with the first total synthesis of (+)- N -(4′-hydroxyprenyl)-cyclo(alanyltryptophyl), which was completed in five steps, starting froml -tryptophan methyl ester hydrochloride.