Total Syntheses of Dihydroindole Aspidosperma Alkaloids: Reductive Interrupted Fischer Indolization Followed by Redox Diversification
Author:
Affiliation:
1. Institute of Organic Chemistry, Research Centre for Natural Sciences, 2 Magyar tudósok krt., Budapest, H-1117, Hungary
2. Instrumentation Center, Research Centre for Natural Sciences, 2 Magyar tudósok krt., Budapest, H-1117, Hungary
Funder
Nemzeti Kutat?si Fejleszt?si ?s Innov?ci?s Hivatal
Publisher
American Chemical Society (ACS)
Subject
Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry
Link
http://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c01472
Reference95 articles.
1. Reviews on synthesis of Aspidosperma and related alkaloids: aSaxton, J. E. In The Alkaloids: Chemistry and Biology; Cordell, G. A., Eds. Academic Press: San Diego, CA, 1998; Vol. 50, pp 343–376.
2. bLopchuk, J. M. In Progress in Heterocyclic Chemistry; Gribble, G. W., Joule, J. A., Eds. Elsevier: Oxford, U.K., 2011; Vol. 23, pp 1–25.
3. A Review on Recent Developments in Syntheses of the Post-Secodine Indole Alkaloids. Part I: The Primary Alkaloid Types
4. A Review on Recent Developments in Syntheses of the post-Secodine Indole Alkaloids. Part II: Modified Alkaloid Types
5. Enantioselective palladium-catalyzed allylic alkylation reactions in the synthesis of Aspidosperma and structurally related monoterpene indole alkaloids
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