Synthesis of Macrolactone Core of <i>ent</i>-Formosalide A via Regioselective Ether Cyclization-Reference-Cited by-同舟云学术

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Synthesis of Macrolactone Core of ent-Formosalide A via Regioselective Ether Cyclization

Published:2024-05-07 Issue:11 Volume:89 Page:7991-8004
ISSN:0022-3263
Container-title:The Journal of Organic Chemistry
language:en
Short-container-title:J. Org. Chem.

Author:

Mozumi Risa¹,Fukaya Keisuke¹^ORCID,Ito Hina¹,Komatsu Tomomi¹,Urabe Daisuke¹^ORCID

Affiliation:

1. Biotechnology Research Center and Department of Biotechnology, Toyama Prefectural University 5180 Kurokawa, Imizu, Toyama 939-0398, Japan

Funder

Ministry of Education, Culture, Sports, Science and Technology

NOVARTIS Foundation (Japan) for the Promotion of Science

Japan Society for the Promotion of Science

Publisher

American Chemical Society (ACS)

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.joc.4c00633

Reference38 articles.

1. Tetrahydrofuran-Containing Macrolides: A Fascinating Gift from the Deep Sea

2. Formosalides A and B, cytotoxic 17-membered ring macrolides from a marine dinoflagellate Prorocentrum sp.

3. The Formosalides: Structure Determination by Total Synthesis

4. Stereoselective Synthesis of the C1–C16 Fragment of the Purported Structure of Formosalide B

5. Computational Prediction of 1H and 13C Chemical Shifts: A Useful Tool for Natural Product, Mechanistic, and Synthetic Organic Chemistry

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