Journal ArticleDOI
Samarium triiodide-catalyzed conjugate addition of indoles with electron-deficient olefins
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In this article, it was shown that the substitution on the indole nucleus occurred exclusively at the 3-position and N -alkylation products have not been observed at the other positions.About:
This article is published in Tetrahedron Letters.The article was published on 2005-05-30. It has received 96 citations till now. The article focuses on the topics: Triiodide & Michael reaction.read more
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Catalytic Functionalization of Indoles in a New Dimension
Marco Bandini,Astrid Eichholzer +1 more
TL;DR: This Review emphasizes the achievements in the selective catalytic functionalization of indoles (C-C bond-forming processes) over the last four years.
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Katalytische Funktionalisierung von Indolen in einer neuen Dimension
Marco Bandini,Astrid Eichholzer +1 more
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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Synthetic approaches to 3-(2-nitroalkyl) indoles and their use to access tryptamines and related bioactive compounds.
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Glycerol as An Efficient Promoting Medium for Organic Reactions
TL;DR: In this article, the use of glycerol as solvent was shown to accelerate the reaction rate of an organic reaction even starting from more hydrophobic substrates than those usually used on water.
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Sulfamic acid-catalyzed Michael addition of indoles and pyrrole to electron-deficient nitroolefins under solvent-free condition
TL;DR: Sulfamic acid (SA) effectively catalyzes the Michael addition of indoles and pyrrole to nitroolefins under solvent-free condition to afford the corresponding Michael adducts in good to excellent yields as discussed by the authors.
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