Tsavoenones A–C: unprecedented polyketides with a 1,7-dioxadispiro[4.0.4.4]tetradecane core from the lichen Parmotrema tsavoense-Reference-Cited by-同舟云学术

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Tsavoenones A–C: unprecedented polyketides with a 1,7-dioxadispiro[4.0.4.4]tetradecane core from the lichen Parmotrema tsavoense

Published:2018 Issue:32 Volume:16 Page:5913-5919
ISSN:1477-0520
Container-title:Organic & Biomolecular Chemistry
language:en
Short-container-title:Org. Biomol. Chem.

Author:

Duong Thuc-Huy¹²³⁴⁵,Beniddir Mehdi A.⁶⁷⁸⁹¹⁰^ORCID,Genta-Jouve Grégory¹¹¹²¹³¹⁴^ORCID,Aree Thammarat¹⁵¹⁶¹⁷¹⁸¹⁹^ORCID,Chollet-Krugler Marylène²⁰⁹²¹²²¹⁴,Boustie Joël²⁰⁹²¹²²¹⁴,Ferron Solenn²⁰⁹²¹²²¹⁴,Sauvager Aurélie²⁰⁹²¹²²¹⁴,Nguyen Huu-Hung²³²⁴²⁵⁴,Nguyen Kim-Phi-Phung²⁶²⁷²⁸²⁵⁴,Chavasiri Warinthorn¹⁵¹⁶¹⁷¹⁸¹⁹,Le Pogam Pierre⁶⁷⁸⁹¹⁰^ORCID

Affiliation:

1. Department for Management of Science and Technology Development

2. Ton Duc Thang University

3. Ho Chi Minh City

4. Vietnam

5. Faculty of Applied Sciences

6. Équipe “Pharmacognosie-Chimie des Substances Naturelles”

7. BioCIS

8. Univ. Paris-Sud

9. CNRS

10. Université Paris-Saclay

11. Équipe C-TAC

12. UMR CNRS 8638 COMETE – Université Paris Descartes

13. 75006 Paris

14. France

15. Natural Products Research Unit

16. Department of Chemistry

17. Faculty of Science

18. Chulalongkorn University

19. Bangkok 10330

20. Univ Rennes

21. ISCR (Institut des Sciences Chimiques de Rennes) – UMR 6226

22. F-35000 Rennes

23. Faculty of Biotechnology and environment

24. Nguyen Tat Thanh University

25. Ho Chi Minh City 748355

26. Department of Organic Chemistry

27. University of Science

28. National University – Ho Chi Minh City

Abstract

Three racemic polyketides with a novel scaffold are reported from the lichen Parmotrema tsavoense.

Funder

Chulalongkorn University

Université de Rennes 1

Publisher

Royal Society of Chemistry (RSC)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2018/OB/C8OB01280F

Reference25 articles.

1. Lichens—a promising source of bioactive secondary metabolites

2. A new depside and two new diphenyl ether compounds from the lichen Ramalina farinacea (L.) Ach

3. New erythritol derivatives from the fertile form of Roccella montagnei

4. Sanctis A-C: Three Racemic Procyanidin Analogues from The Lichen Parmotrema sancti-angelii

5. New meta -depsidones and diphenyl ethers from the lichen Parmotrema tsavoense (Krog & Swinscow) Krog & Swinscow, Parmeliaceae

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2. Two New α‐Glucosidase Inhibitory Depsidones from the Lichen Parmotrema cristiferum (Taylor) Hale;Chemistry & Biodiversity;2023-03

3. Lichens in Pharmacological Action: What Happened in the Last Decade?;The Eurasian Journal of Medicine;2023-01-18

4. Myrrhalindenane C, a New Eudesmane Sesquiterpenoid From Lindera Myrrha Roots;Records of Natural Products;2023-01-01

5. Demystifying racemic natural products in the homochiral world;Nature Reviews Chemistry;2022-10-14

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