Asymmetric synthesis of the perhydroepoxyethanoindole core <i>via</i> sequential [4 + 2]-addition/reduction/fluoroannulation reactions-Reference-Cited by-同舟云学术

Asymmetric synthesis of the perhydroepoxyethanoindole core via sequential [4 + 2]-addition/reduction/fluoroannulation reactions

Published:2023 Issue:2 Volume:21 Page:339-344
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Prasad Madavi S.¹^ORCID,Sivaprakash Murugesan¹

Affiliation:

1. Asymmetric synthesis and catalysis laboratory, Department of Chemistry, Central University of Tamil Nadu (CUTN), Tiruvarur-610 005, India

Abstract

Asymmetric synthesis of fluoro-perhydroepoxyethanoindole was achieved through a sequential aminocatalytic [4 + 2]-addition/reduction/fluoroannulation reactions.

Funder

Science and Engineering Research Board

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2023/OB/D2OB02058K

Reference55 articles.

1. J. E.Saxton , Alkaloids of the Aspidospermine Group , in The Alkaloids, Chemistry and Biology , ed. G. A. Cordell , Academic Press , San Diego , 1998 , vol. 51 , pp. 1–197

2. S. E.O'Connor , Alkaloids , in Comprehensive Natural Products II , Elsevier , Amsterdam , 2010 , vol. 1 , pp. 977–1007

3. Alkaloid studies XLII. The structures of dichotamine, 1-acetyl-aspidoalbidine and 1-acetyl-17-hydroxyaspidoalbidine: three new alkaloids from ruiz et pav

4. Alkaloid-Studien LII. Die Alkaloide ausVallesia dichotoma RUIZet PAV

5. The total synthesis of the alkaloid (±)-1-acetylaspidoalbidine

Cited by 6 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Developments in Organocatalysis Transformations of Unsaturated Pyrazolones;Current Organic Synthesis;2024-06-21

2. Amine Catalyzed Remote [4+2]‐annulation Of Indole Tethered Enal And Oxindole Olefin To Access Optically Pure Hydrocarbazole Spirooxindole Scaffolds;Asian Journal of Organic Chemistry;2024-03-06

3. Enantioselective Synthesis of Octahydrofuranoindole Core of Aspidosperma Alkaloids via a Diels‐Alder/Reduction/Fluoroetherification Reaction Sequence;Chemistry – An Asian Journal;2023-07-20

4. Blossoming of Polyenamine Catalysis in Asymmetric Synthesis: Scope and Future Applications;Chemistry – An Asian Journal;2023-05-25

5. N-2,2,2-Trifluoroethylisatin ketimine as a 1,2-dipolarophile for [3 + 2]-addition to access optically pure spirothiazolidine oxindoles;Organic & Biomolecular Chemistry;2023