ChemInform Abstract: Observations Concerning the Synthesis of Tryptamine Homologues and Branched Tryptamine Derivatives via the Borrowing Hydrogen Process: Synthesis of Psilocin, Bufotenin, and Serotonin.
Silvia Bartolucci, Michele Mari, Giovanni Di Gregorio, Giovanni Piersanti
ChemInform July 1, 2016 DOI: 10.1002/chin.201633131
Summary
AI-generated from the abstractA new chemical method for selective indole alkylation uses iridium catalysis and a borrowing hydrogen strategy with amino alcohols as nitrogen-containing electrophiles. The reaction produces alkylated indole products, offering a synthetic route that avoids pre-functionalized starting materials.
Study at a glance
| Characteristics | Experimental study Peer reviewed |
|---|---|
| Key finding | Ir-catalyzed borrowing hydrogen methodology enables selective indole alkylation using amino alcohols as nitrogen-containing electrophiles. |
Abstract
AbstractThe selective indole alkylation reaction applying the Ir‐catalyzed‐borrowing hydrogen methodology and using amino alcohols (II), (V), (VII) as suitable nitrogen‐containing electrophiles is reported.