Bioinspired synthesis and biological evaluation of <i>ent</i>-protulactones A and B-Reference-Cited by-同舟云学术

Bioinspired synthesis and biological evaluation of ent-protulactones A and B

Published:2024 Issue:1 Volume:22 Page:175-183
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Liang Changxu¹²,Hu Chao¹,Nie Pengpeng¹²,Liu Yuanfang¹²,Liu Jun¹²³^ORCID,Du Yuguo¹²³

Affiliation:

1. State Key Laboratory of Environmental Chemistry and Eco-toxicology, Research Center for Eco-Environmental Sciences, Chinese Academy of Sciences, Beijing 100085, China

2. School of Chemical Sciences, University of Chinese Academy of Sciences, Beijing 100049, China

3. Binzhou Institute of Technology, Weiqiao-UCAS Science and Technology Park, Binzhou 256606, Shandong Province, China

Abstract

The bioinspired and stereoselective synthesis of the furo[3,2-b] furan lactone (−)-protulactone A and the dioxabicyclo[3.3.1]nonane lactone (+)-protulactone B has been achieved based on the chiron approach.

Funder

Chinese Academy of Sciences

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2024/OB/D3OB01708G

Reference17 articles.

1. Polyketides as Secondary Metabolites from the Genus Aspergillus

2. Protulactones A and B: Two New Polyketides from the Marine-derived Fungus Aspergillus sp. SF-5044

3. Novel bioactive styryl-lactones: goniofufurone, goniopypyrone, and 8-acetylgoniotriol from Goniothalamus giganteus(annonaceae). X-Ray molecular structure of goniofufurone and of goniopypyrone

4. Total Synthesis, Configuration Assignment, and Cytotoxic Activity Evaluation of Protulactone A

5. Stereoselective synthesis of (−)-protulactone A