Rapid Synthesis of Functionalized Hydrocarbazolones via Indole C2−H Activation Using Enone Functionality as a Directing Group/Electrophilic Species
Author:
Affiliation:
1. Graduate School of Pharmaceutical Sciences Chiba University 1-8-1, Inohana, Chuo-ku Chiba 260-8675 Japan
2. Molecular Chirality Research Center Chiba University 1-33, Yayoi-cho, Inage-ku Chiba 263-8522 Japan
Funder
Novartis
Futaba Electronics Memorial Foundation
Chiba University
Publisher
Wiley
Subject
General Chemistry
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/adsc.202100098
Reference72 articles.
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2. Thiourea-Catalyzed Asymmetric Michael Addition of Carbazolones to 2-Chloroacrylonitrile: Total Synthesis of 5,22-Dioxokopsane, Kopsinidine C, and Demethoxycarbonylkopsin
3. Total synthesis of indole alkaloids. A new strategy for (.+-.)-19-oxoaspidospermidine and (.+-.)-19-oxoaspidofractinine
4. Reactivity of hexahydrocarbazol-4-ones in Michael reactions: stereocontrolled formation of decahydropyrido[2,3-d ]carbazoles
5. Concise total synthesis of (±)-aspidospermidine
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1. Advances in Transition-Metal-Catalyzed Keto Carbonyl-Directed C—H Bond Functionalization Reactions;Chinese Journal of Organic Chemistry;2023
2. Synthesis of Tetrahydrocarbazol-4-ones via Rh(III)-Catalyzed C–H Activation/Annulation of Arylhydrazines with Iodonium Ylides;The Journal of Organic Chemistry;2022-06-08
3. Transition‐Metal‐Catalyzed C−H Bond Functionalization of Arenes/Heteroarenes via Tandem C−H Activation and Subsequent Carbene Migratory Insertion Strategy;The Chemical Record;2021-10-14
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