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- A comparison of structural–functional equation models to identify fatty acids on three common gas chromatography columns. A. T. L. Wotherspoon, K. L. Reeves, J. Crawford
, Anal. Methods
, 2018
, 10
, 1747
- Synthesis of toluene-4-sulfonic acid 2-(2-thiophen-2-yl-phenanthro[9,10-d]imidazol-1-yl)-ethyl ester and its application for sensitive determination of free fatty acids in ginkgo nut and ginkgo leaf by high performance liquid chromatography with fluorescence detection. Xiuli Dong, Xueying Liu, Xiangming Chen
, RSC Adv.
, 2018
, 8
, 18549
- The biosynthesis of a graphene oxide-based zinc oxide nanocomposite using Dalbergia latifolia leaf extract and its biological applications. Elavarasan Nagaraj, Prakash Shanmugam, Kokila Karuppannan, Thirunavukkarasu Chinnasamy, Sujatha Venugopal
, New J. Chem.
, 2020
, 44
, 2166
- Efficient biomass transformations catalyzed by graphene-like nanoporous carbons functionalized with strong acid ionic liquids and sulfonic groups. Fujian Liu, Weiping Kong, Liang Wang, Xianfeng Yi, Iman Noshadi, Anmin Zheng, Chenze Qi
, Green Chem.
, 2015
, 17
, 480
- Synthesis of novel heterocyclic oleanolic acid derivatives with improved antiproliferative activity in solid tumor cells. Ana S. Leal, Rui Wang, Jorge A. R. Salvador, Yongkui Jing
, Org. Biomol. Chem.
, 2013
, 11
, 1726
- A review: the botany, ethnopharmacology, phytochemistry, pharmacology of Cinnamomi cortex. Songtao Liu, Liu Yang, Senwang Zheng, Ajiao Hou, Wenjing Man, Jiaxu Zhang, Song Wang, Xuejiao Wang, Huan Yu, Hai Jiang
, RSC Adv.
, 2021
, 11
, 27461
- Citrus limetta fruit waste management by liquefaction using hydrogen-donor solvent. Sneha Acharya, Nanda Kishore
, RSC Adv.
, 2022
, 12
, 32708
- The thermotropic phase behaviour of phyto-ceramide 1 as investigated by ATR-FTIR and DSC. Patrick Garidel
, Phys. Chem. Chem. Phys.
, 2002
, 4
, 2714
- The polarisabilities of bonds. Part II.—bond refractions in the alkanes. B. C. Vickery, K. G. Denbigh
, Trans. Faraday Soc.
, 1949
, 45
, 61
- The cathodic reduction of activated olefins. Experimental conditions allowing the specific hydrogenation of the enone derived from ergosterol. C. Brosa, C. Rodríguez-Santamarta, J. F. Pilard, J. Simonet
, Phys. Chem. Chem. Phys.
, 2001
, 3
, 2655