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Synthesis of prenylated indoles

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This article is published in Journal of Organic Chemistry.The article was published on 1986-06-01. It has received 65 citations till now. The article focuses on the topics: Bicyclic molecule & Acylation.

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Catalytic Functionalization of Indoles in a New Dimension

TL;DR: This Review emphasizes the achievements in the selective catalytic functionalization of indoles (C-C bond-forming processes) over the last four years.
Journal ArticleDOI

Pd-catalyzed C3-selective allylation of indoles with allyl alcohols promoted by triethylborane.

TL;DR: Under palladium catalysis, Et3B nicely promotes allyl alcohols to undergo C3-selective allylation of indoles and tryptophan; the yields range 75-95%.
Journal ArticleDOI

Katalytische Funktionalisierung von Indolen in einer neuen Dimension

TL;DR: In this paper, the Fortschritte hinsichtlich der selektiven katalytischen Funktionalisierung von Indolen (durch C-C-Kupplung) aus den vergangenen vier Jahre zusammen.
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Palladium(0)-Catalyzed Heteroarylation of 2- and 3-Indolylzinc Derivatives. An Efficient General Method for the Preparation of (2-Pyridyl)indoles and Their Application to Indole Alkaloid Synthesis.

TL;DR: From 2-(2-pyridyl)indole 4b, a new synthetic entry to the indolo[2,3-a]quinolizidine system, involving stereoselective hydrogenation of the pyridine ring with subsequent electrophilic cyclization upon the indole 3-position from an appropriately N(b)-substituted 2-piperidyl-indole, is reported.
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