Concise approach to 1,4-dioxygenated xanthones via novel application of the Moore rearrangement-Reference-Cited by-同舟云学术

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Concise approach to 1,4-dioxygenated xanthones via novel application of the Moore rearrangement

Published:2012-09 Issue:37 Volume:68 Page:7591-7597
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Nichols Alexander L.,Zhang Patricia,Martin Stephen F.

Funder

National Institutes of Health

Robert A. Welch Foundation

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference33 articles.

1. Inhibitors of bone resorption from Halenia corniculata

2. A xanthone from Garcinia atroviridis

3. Total synthesis of atroviridin

4. Xanthone Natural Products via N-Heterocyclic Carbene Catalysis: Total Synthesis of Atroviridin

5. Structure of cervinomycin, a novel antianaerobic antibiotic

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1. Chemistry and biosynthesis of bacterial polycyclic xanthone natural products;Natural Product Reports;2022

2. Toward the total synthesis of citreamicin η: Synthesis of the pentacyclic core and GAB-ring annelation model studies;Tetrahedron;2018-09

3. A Thermally Induced Hydride Transfer from an Amine to an Allene Triggers an Annulation Reaction, Giving Dihydrofuropyridinones;Organic Letters;2018-07-03

4. Syntheses of Asymmetrically Substituted Pyrans of Natural Origin;Natural Products as Source of Molecules with Therapeutic Potential;2018

5. Natural Products and Their Mimics as Targets of Opportunity for Discovery;The Journal of Organic Chemistry;2017-09-15

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