A Cobalt-Catalyzed Entry Into the Ergot Alkaloids: Total Syntheses of (±)-Lysergene and (±)-LSD
Carlos Saá, Dallas D. Crotts, Gishun Hsu, K. Peter C. Vollhardt
Study at a glance
AI-extracted from the abstract| Characteristics | Peer reviewed |
|---|---|
| Topics | LSD |
| Citations | 71 |
Abstract
All articles of this category Cocyclization of 4 -ethynyl-3-indoleacetonitriles with alkynes in the presence of CpCo(CO) 2 gives rise to the ergoline derivatives 6-9 , two of which were transformed into racemic lysergene and LSD, respectively.
Citations in the library
Cited by 3
- Synthetic Strategies toward Lysergic Acid Diethylamide: Ergoline Synthesis via α-Arylation, Borrowing Hydrogen Alkylation, and C-H Insertion. The Journal of Organic Chemistry October 6, 2023
- Solving a Mystery with Classical and Dual Photoredox Catalysis: Application of Nickel in the Synthesis of Ergot Alkaloids. Organic Letters May 24, 2024
- ChemInform Abstract: A Cobalt‐Catalyzed Entry into the Ergot Alkaloids: Total Syntheses of ( .+‐.)‐Lysergene (VII) and (.+‐.)‐LSD. ChemInform December 20, 1994