Wacker oxidation methodology for the synthesis of the benzo-fused acetal core of marticin-Reference-Cited by-同舟云学术

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Wacker oxidation methodology for the synthesis of the benzo-fused acetal core of marticin

Published:2012-09 Issue:35 Volume:68 Page:7116-7121
ISSN:0040-4020
Container-title:Tetrahedron
language:en
Short-container-title:Tetrahedron

Author:

Pillay Adushan,Rousseau Amanda L.,Fernandes Manuel A.,de Koning Charles B.

Funder

SABINA

National Research Foundation

Pretoria

University of the Witwatersrand

Publisher

Elsevier BV

Subject

Organic Chemistry,Drug Discovery,Biochemistry

Reference14 articles.

1. The marticins: confirmation of structure, elucidation of biosynthetic origin by 13Cmr studies, and revision of stereochemical assignments

2. Pyranonaphthoquinone antibiotics—isolation, structure and biological activity

3. Averufin in the biosynthesis of aflatoxin B1

4. Isagarin, a New Type of Tetracyclic Naphthoquinone from the Roots of Pentas longiflora

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1. Quinacetophenone: A simple precursor to privileged organic motifs;Arabian Journal of Chemistry;2019-12

2. Palladium catalyzed C–H bond acetoxylation: isoxazolinyl as a directing group;RSC Advances;2016

3. Wacker Oxidation, The;Organic Reactions;2014-04-12

4. One-pot access to 2-naphthols and benzofurans via the aerobic Wacker-type oxidation/intramolecular aldol cyclization;Tetrahedron;2013-02

5. (Z)-Ethyl 2-hydroxy-4-oxo-4-(1,4,5,6,8-pentamethoxynaphthalen-2-yl)but-2-enoate;Acta Crystallographica Section E Structure Reports Online;2012-12-08

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