Synthesis of Tetrahydro-β-carbolines and Studies of the Pictet–Spengler Reaction
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference11 articles.
1. A new diastereoselective synthesis of (±) cis 1-aminoindoloquinolizidine
2. Stereospecific pictet-spengler reaction: synthesis of cis (+)-(1S, 12bR)-1-aminoindoloquinolizidine from a pure α-(S)-aminoaldehyde derivative
3. The Pictet-Spengler condensation: a new direction for an old reaction
4. I. Selective Protection of α- or Side-chain Carboxyl Groups of Aspartic and Glutamic Acid. A Facile Synthesis of β-Aspartyl and γ-Glutamyl Peptides
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1. Metal-free access to β-carbolines via single-electron transfer catalyzed by a triaryl carbenium ion pair;Cell Reports Physical Science;2023-02
2. Indolethylamine N-methyltransferase (INMT) is not essential for endogenous tryptamine-dependent methylation activity in rats;Scientific Reports;2023-01-06
3. References;Microbial Metabolism and Disease;2021
4. Inverted Binding of Non-natural Substrates in Strictosidine Synthase Leads to a Switch of Stereochemical Outcome in Enzyme-Catalyzed Pictet–Spengler Reactions;Journal of the American Chemical Society;2020-01-07
5. An overview on synthetic entries to tetrahydro-β-carbolines;Tetrahedron;2019-02
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