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Asymmetric Total Syntheses of (-)-Ervatamine and (+)-19,20-Dehydroervatamine via Late-Stage Directed Indolization
- Authors
- Chen, Qinyang; Jeon, Da-Yun; Cho, Cheon-Gyu
- Issue Date
- Jul-2025
- Publisher
- American Chemical Society
- Citation
- Organic Letters, v.27, no.29, pp 7744 - 7749
- Pages
- 6
- Indexed
- SCIE
SCOPUS
- Journal Title
- Organic Letters
- Volume
- 27
- Number
- 29
- Start Page
- 7744
- End Page
- 7749
- ISSN
- 1523-7060
1523-7052
- Abstract
- Asymmetric total syntheses of (-)-ervatamine and (+)-19,20-dehydroervatamine are described. The key is the directed, late-stage implementation of the indole unit, enabled by the strategically installed ketone group in the central cycloheptene ring.
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Related Researcher
- Cho, Cheon Gyu
- COLLEGE OF NATURAL SCIENCES (DEPARTMENT OF CHEMISTRY)