Light/inductive effect induced isomerization of chromeno-5-methyl-2,6,9-trioxabicyclo[3.3.1]nonadienes-Reference-Cited by-同舟云学术

Light/inductive effect induced isomerization of chromeno-5-methyl-2,6,9-trioxabicyclo[3.3.1]nonadienes

Published:2020 Issue:25 Volume:44 Page:10195-10198
ISSN:1144-0546
Container-title:New Journal of Chemistry
language:en
Short-container-title:New J. Chem.

Author:

Vyasamudri Sameer¹²³^ORCID,Yang Ding-Yah¹²³⁴²^ORCID

Affiliation:

1. Department of Chemistry

2. Tunghai University

3. Taiwan

4. Graduate Program for Biomedical and Materials Science

Abstract

An efficient rearrangement of coumarin-based trioxabicycles and the effect of UV light and electron-withdrawing substituents on this transformation are reported.

Funder

Ministry of Science and Technology, Taiwan

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,General Chemistry,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2020/NJ/D0NJ02288H

Reference22 articles.

1. Structure of preussomerin A: an unusual new antifungal metabolite from the coprophilous fungus Preussia isomera

2. The preussomerins: novel antifungal metabolites from the coprophilous fungus Preussia isomera Cain

3. Preussomerin D from the Endophyte Hormonema Dematioides

4. Preussomerins and Deoxypreussomerins: Novel Inhibitors of Ras Farnesyl-Protein Transferase

5. Sporovexins A−C and a New Preussomerin Analog: Antibacterial and Antifungal Metabolites from the Coprophilous Fungus Sporormiella vexans

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