Synthetic Efforts toward Lannotinidine G Based on an Aziridinium-Mediated Ring Contraction and Dienyne Metathesis-Reference-Cited by-同舟云学术

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Synthetic Efforts toward Lannotinidine G Based on an Aziridinium-Mediated Ring Contraction and Dienyne Metathesis

Published:2024-04-02 Issue:15 Volume:26 Page:3184-3188
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Peitsinis Zisis¹,Trauner Dirk¹²^ORCID

Affiliation:

1. Department of Chemistry, New York University, New York, New York 10003, United States

2. Department of Chemistry and Department of Systems Pharmacology and Translational Therapeutics, University of Pennsylvania, Philadelphia, Pennsylvania 19104, United States

Funder

Division of Chemistry

New York University

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.4c00791

Reference26 articles.

1. Lannotinidines A–G, new alkaloids from two species of Lycopodium

2. Lycopodin, das erste Alkaloïd der Gefässkryptogamen

3. Protecting Group-Free Total Synthesis of (−)-Lannotinidine B

4. Synthesis of Optically Active 5-(tert-Butyldimethylsiloxy)-2-cyclohexenone and Its 6-Substituted Derivatives as Useful Chiral Building Blocks for the Synthesis of Cyclohexane Rings. Syntheses of Carvone, Penienone, and Penihydrone

5. Enantiomerically pure β,γ-epoxyesters from β-hydroxylactones: synthesis of β-hydroxyesters and (-)-GABOB

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