Synthesis of Naturally Occurring Pyranonaphthoquinones: (±) 9-Demethoxyeleutherin, (±) 9-Demethoxyisoeleutherin, and Pentalongin via Nef Reaction
Author:
Affiliation:
1. a Postgraduate and Research Centre, Department of Chemistry , MES Abasaheb Garware College , Pune , India
Funder
The authors thank the Department of Science and Technology–Funding for Infrastructure in Science and Technology for an infrastructure grant. R. A. L. is thankful to the University Grants Commission for a senior research fellowship.
Publisher
Informa UK Limited
Subject
Organic Chemistry
Link
https://www.tandfonline.com/doi/pdf/10.1080/00397911.2014.905600
Reference16 articles.
1. Synthesis of deoxyfrenolicin and nanaomycin A
2. Pyranonaphthoquinone antibiotics—isolation, structure and biological activity
3. Pyranonaphthoquinone derivatives of eleutherin, ventiloquinone L, thysanone and nanaomycin A possessing a diverse topoisomerase II inhibition and cytotoxicity spectrum
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1. Pyranonaphthoquinones – isolation, biology and synthesis: an update;Natural Product Reports;2017
2. The Nitro to Carbonyl Conversion (Nef Reaction): New Perspectives for a Classical Transformation;Advanced Synthesis & Catalysis;2015-07-29
3. Expedient stereoselective synthesis of new dihydropyrano- and dihydrofuranonaphthoquinones;Tetrahedron Letters;2015-05
4. Convenient Syntheses of 3-Aryl-3,4-Dihydroisocoumarins;Journal of Chemical Research;2015-04
5. Convenient synthesis of Bioactive Pyranonaphthoquinones (±)9-Demethoxyeleutherin and (±)9-Demethoxyisoeleutherin;Journal of Chemical Research;2014-09
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