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- Bio-inspired construction of a tetracyclic ring system with an avarane skeleton: total synthesis of dactyloquinone A. Yumeng Wu, Xuanxuan Du, Xianyang Wang, Hainan Liu, Luning Zhou, Yu Tang, Dehai Li
, Org. Chem. Front.
, 2022
, 9
, 4705
- Natural 6-hydroxy-chromanols and -chromenols: structural diversity, biosynthetic pathways and health implications. Marc Birringer, Karsten Siems, Alexander Maxones, Jan Frank, Stefan Lorkowski
, RSC Adv.
, 2018
, 8
, 4803
- Natural sesquiterpenoids. Braulio M. Fraga
, Nat. Prod. Rep.
, 2003
, 20
, 392
- Isoflavonoids of the Leguminosae. Nigel C. Veitch
, Nat. Prod. Rep.
, 2009
, 26
, 776
- Antifungal mono- and dimeric nitrogenous bisabolene derivatives from a sponge in the order Bubarida from Futuna Islands. Maria Miguel-Gordo, Maggie M. Reddy, Pilar Sánchez, Jordan J. Buckley, Thomas A. Mackenzie, Laurence K. Jennings, Fernando Reyes, Kevin Calabro, Olivier P. Thomas
, Org. Biomol. Chem.
, 2022
, 20
, 1031
- Marine organisms as potential sources of natural products for the prevention and treatment of malaria. Walaa A. Negm, Shahira M. Ezzat, Ahmed Zayed
, RSC Adv.
, 2023
, 13
, 4436
- Natural sesquiterpene quinone/quinols: chemistry, biological activity, and synthesis. Xin-Hui Tian, Li-Li Hong, Wei-Hua Jiao, Hou-Wen Lin
, Nat. Prod. Rep.
, 2023
, 40
, 718
- An invocation for computational evaluation of isomerization transforms: cationic skeletal reorganizations as a case study. Alexander W. Schuppe, Yannan Liu, Timothy R. Newhouse
, Nat. Prod. Rep.
, 2021
, 38
, 510
- Copper-catalyzed intramolecular cross dehydrogenative coupling approach to coumestans from 2′-hydroxyl-3-arylcoumarins. Xianheng Song, Xiang Luo, Jianfei Sheng, Jianheng Li, Zefeng Zhu, Zhibo Du, Hui Miao, Meng Yan, Mingkang Li, Yong Zou
, RSC Adv.
, 2019
, 9
, 17391
- Marine natural products from sponges (Porifera) of the order Dictyoceratida (2013 to 2019); a promising source for drug discovery. Enas Reda Abdelaleem, Mamdouh Nabil Samy, Samar Yehia Desoukey, Miaomiao Liu, Ronald J. Quinn, Usama Ramadan Abdelmohsen
, RSC Adv.
, 2020
, 10
, 34959