Projects per year
Abstract
Despite the enormous developments in the asymmetric transformations of indole imine methides (IIMs), the remote asymmetric induction involving IIMs remains challenging due to the spatial interaction requirement between the substrate and catalyst. Herein we report the first catalytic asymmetric nucleophilic addition to indole imine 5-methide (5-IIM), the only topological isomer of IIMs whose asymmetric addition remains unknown. Despite the challenging remote stereocontrol, high efficiency and respectable enantioselectivity were achieved to provide access to a range of enantioenriched indole-containing triaryl alkanes.
| Original language | English |
|---|---|
| Pages (from-to) | 396-400 |
| Number of pages | 5 |
| Journal | Organic Letters |
| Volume | 26 |
| Issue number | 1 |
| DOIs | |
| Publication status | Published - 12 Jan 2024 |
Bibliographical note
Publisher Copyright:© 2024 American Chemical Society.
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Dive into the research topics of 'Organocatalytic Enantioselective Nucleophilic Addition of Indole Imine 5-Methides'. Together they form a unique fingerprint.Projects
- 5 Finished
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Organocatalytic Asymmetric Construction of All-Carbon Quaternary Stereocenters in Congested Systems
SUN, J. (PI)
1/01/23 → 31/12/25
Project: Research
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Chiral Phosphoric Acid-Catalyzed Asymmetric Electrochemical Transformations
SUN, J. (PI) & TAN, X. (CoI)
1/07/22 → 30/06/25
Project: Research
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Development of a New Generation of Privileged Chiral Catalysts for Asymmetric Synthesis
LIN, Z. (CoPI), CHIU, P. (CoPI) & SUN, J. (PI)
RGC - Collaborative Research Fund
30/06/22 → 29/06/25
Project: Research