An Enantiospecific Synthesis of Isoneoamphilectane Confirms Its Strained Tricyclic Structure-Reference-Cited by-同舟云学术

An Enantiospecific Synthesis of Isoneoamphilectane Confirms Its Strained Tricyclic Structure

Published:2023-02-02 Issue:6 Volume:145 Page:3716-3726
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Dwulet Natalie C.¹,Chahine Zeinab²,Le Roch Karine G.²,Vanderwal Christopher D.¹³^ORCID

Affiliation:

1. Department of Chemistry, University of California, Irvine, California 92697-2025, United States

2. Institute for Integrative Genome Biology, Center for Infectious Disease and Vector Research, 900 University Avenue, Department of Molecular, Cell, and Systems Biology, University of California, Riverside, California 92521, United States

3. Department of Pharmaceutical Sciences, 101 Theory, University of California, Irvine, California 92697, United States

Funder

National Institute of Allergy and Infectious Diseases

Division of Graduate Education

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/jacs.2c13137

Reference58 articles.

1. Syntheses and biological studies of marine terpenoids derived from inorganic cyanide

2. Novel Potent Antimalarial Diterpene Isocyanates, Isothiocyanates, and Isonitriles from the Tropical Marine Sponge Cymbastela hooperi

3. Antimalarial Activity: The Search for Marine-Derived Natural Products with Selective Antimalarial Activity

4. Antimalarial Activity of Sesquiterpenes from the Marine Sponge Acanthella klethra

5. Two Rare-Class Tricyclic Diterpenes with Antitubercular Activity from the Caribbean Sponge Svenzea flava. Application of Vibrational Circular Dichroism Spectroscopy for Determining Absolute Configuration

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