A Raney Cobalt Mediated Reductive Cyclization Route to the Uleine Alkaloid Gilbertine
Author:
Affiliation:
1. Research School of Chemistry, Institute of Advanced Studies, The Australian National University, Canberra, ACT 2601, Australia
Funder
Australian Research Council
Institute of Advanced Studies
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry
Link
https://pubs.acs.org/doi/pdf/10.1021/acs.joc.6b01424
Reference24 articles.
1. Gilbertin, ein neuer indolalkaloidtyp
2. Palladium-Catalyzed Ullmann Cross-Coupling/Tandem Reductive Cyclization Route to Key Members of the Uleine Alkaloid Family
3. Alkaloids from alstonia undulifolia
4. Alstilobanines A–E, new indole alkaloids from Alstonia angustiloba
5. Enantioselective Synthesis of (−)-Gilbertine via a Cationic Cascade Cyclization
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1. Total Synthesis of (+)-Gilbertine: A Cyclopentanone-Based Approach;Organic Letters;2022-10-03
2. Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H;Angewandte Chemie International Edition;2021-04-23
3. Enantioselective Total Synthesis of (+)‐Alstilobanine C, (+)‐Undulifoline, and (−)‐Alpneumine H;Angewandte Chemie;2021-04-23
4. The Palladium-Catalyzed Ullmann Cross-Coupling Reaction: A Modern Variant on a Time-Honored Process;Accounts of Chemical Research;2018-07-16
5. Palladium-Catalyzed Ullmann Cross-Coupling of β-Iodoenones and β-Iodoacrylates with o-Halonitroarenes or o-Iodobenzonitriles and Reductive Cyclization of the Resulting Products To Give Diverse Heterocyclic Systems;Organic Letters;2018-04-20
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