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Search for "α-carboline" in Full Text gives 3 result(s) in Beilstein Journal of Organic Chemistry.
Recent advances and perspectives in ruthenium-catalyzed cyanation reactions
Beilstein J. Org. Chem. 2022, 18, 37–52, doi:10.3762/bjoc.18.4
- investigated the cyanation of differently substituted 7-azaindoles and achieved excellent results. They also succeeded in applying this strategy to N-aryl-α-carbolines to synthesize the respective cyanated N-aryl-α-carboline products. 3 Photocatalyzed cyanation reactions Nowadays photocatalysis has emerged as
Recent advances on organic blue thermally activated delayed fluorescence (TADF) emitters for organic light-emitting diodes (OLEDs)
Beilstein J. Org. Chem. 2018, 14, 282–308, doi:10.3762/bjoc.14.18
An intramolecular inverse electron demand Diels–Alder approach to annulated α-carbolines
Beilstein J. Org. Chem. 2012, 8, 829–840, doi:10.3762/bjoc.8.93
- library of eighty-eight α-carbolines was prepared by using this robust methodology for biological evaluation. Keywords: α-carboline; chemical diversity; inverse electron demand Diels–Alder; isatin; pyrido[2,3-b]indole; 1,2,4-triazine; Introduction In comparison with the well-known β-carbolines, α
- -carboline alkaloids are quite rare, and only a few natural products isolated to date contain this pyrido[2,3-b]indole (α-carboline, 1, Figure 1) core. The most prominent examples are grossularine-1 (2) and grossularine-2 (3), which are marine cytotoxic agents that were isolated from the tunicate Dendrodoa
- the pyrolysis of proteins [10][11] as well as the pyrolysis of tryptophan [12]. Isoeudistomin U, isolated from the ascidian Lissoclinum fragile, was originally reported to have an α-carboline skeleton [13], but this assignment was later shown to be incorrect [14]. Given their isomeric relationship to
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