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- Artemisinic acid: A promising molecule potentially suitable for the semi-synthesis of artemisinin. Jianqiang Kong, Yan Yang, Wei Wang, Kedi Cheng, Ping Zhu
, RSC Adv.
, 2013
, 3
, 7622
- A short synthesis of the 6-epi-arteannuin B skeleton. John R. Williams, Thomas P. Cleary
, J. Chem. Soc., Chem. Commun.
, 1982
, 626
- Recent advances in the synthesis of natural multifunctionalized decalins. S. Dhambri, S. Mohammad, O. Nguyen Van Buu, G. Galvani, Y. Meyer, M.-I. Lannou, G. Sorin, J. Ardisson
, Nat. Prod. Rep.
, 2015
, 32
, 841
- Future antimalarials from Artemisia? A rationale for natural product mining against drug-refractory Plasmodium stages. Alexandre Maciuk, Dominique Mazier, Romain Duval
, Nat. Prod. Rep.
, 2023
, 40
, 1130
- Artemisinin as a therapeutic vs. its more complex Artemisia source material. Pamela J. Weathers
, Nat. Prod. Rep.
, 2023
, 40
, 1158
- Synergy and antagonism in natural product extracts: when 1 + 1 does not equal 2. Lindsay K. Caesar, Nadja B. Cech
, Nat. Prod. Rep.
, 2019
, 36
, 869
- Thermal and Lewis acid promoted intramolecular Diels–Alder reaction of furanose tethered 1,3,9-decatriene systems: a synthetic and computational investigation. Hanuman P. Kalmode, Dilip K. Maity, Prakash M. Bhate
, RSC Adv.
, 2016
, 6
, 63445
- Synthesis of artemisinic acid derived glycoconjugates and their anticancer studies. Tharun K. Kotammagari, Sayantan Paul, Ganesh K. Barik, Manas K. Santra, Asish K. Bhattacharya
, Org. Biomol. Chem.
, 2020
, 18
, 2252
- Selective Reduction of the Exomethylene Group of α-Methylene γ- or δ-Lactones with CdCl2–Mg–MeOH–H2O‡. Asish K. Bhattacharya, Dharam C. Jain, Ram P. Sharma
, J. Chem. Res. (S)
, 1998
, 768
- The biosynthesis of C5–C25 terpenoid compounds. Paul M. Dewick
, Nat. Prod. Rep.
, 1997
, 14
, 111