Stereocontrolled Total Synthesis of (−)-Isocelorbicol and Its Elaboration to Natural Dihydro-β-agarofuran Esters-Reference-Cited by-同舟云学术

Stereocontrolled Total Synthesis of (−)-Isocelorbicol and Its Elaboration to Natural Dihydro-β-agarofuran Esters

Published:2020-11-23 Issue:23 Volume:22 Page:9234-9238
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Mohri Tomoyo¹,Takahashi Yusuke¹,Kwon Eunsang²,Kuwahara Shigefumi¹,Ogura Yusuke¹³^ORCID

Affiliation:

1. Graduate School of Agricultural Science, Tohoku University, Sendai 980-8572, Japan

2. Research and Analytical Center for Giant Molecules, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

3. Department of Applied Biological Chemistry, Graduate School of Agricultural and Life Sciences, The University of Tokyo, 1-1-1 Yayoi, Bunkyo-ku, Tokyo 113-8657, Japan

Funder

Kato Memorial Bioscience Foundation

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.0c03419

Reference26 articles.

1. Celastraceae sesquiterpenoids: biological activity and synthesis

2. The dihydro-β-agarofuran sesquiterpenoids

3. Medicinal chemistry and pharmacology of genus Tripterygium (Celastraceae)

4. Übersicht über die celastraceen-inhaltsstoffe: Chemie, chemotaxonomie, biosynthese, pharmakologie

5. Total Synthesis of the Sesquiterpenoid Polyols (±)-Euonyminol and (±)-3,4-Dideoxymaytol, Core Constituents of Esters of the Celastraceae

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