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- Convenient source of ‘naked’ fluoride: tetra-n-butylammonium chloride and potassium fluoride dihydrate. Louis A. Carpino, Arjun C. Sau
, J. Chem. Soc., Chem. Commun.
, 1979
, 514
- Formation of methyl 2,6-anhydro-3,4-O-isopropylidene-α-and -β-D-talopyranosides by an intramolecular displacement in the methanolysis of 1,6-anhydro-3,4-O-isopropylidene-2-O-methylsulphonyl-β-D-galactopyranose. N. A. Hughes
, J. Chem. Soc. C
, 1969
, 2263
- Rapid spectrophotometric determination of cobalt in high-speed steels based on the formation of tricarbonatocobaltate(III). A. Sanz Medel, A. Cobo Guzmán, J. A. Pérez-Bustamante
, Analyst
, 1976
, 101
, 860
- Hollow hematite single crystals deposited with ultra-thin Al2O3 by atom layer deposition for improved photoelectrochemical performance. Wei Jiao, Jingrui Wu, Siwen Cui, Ning Wei, Zia Ur Rahman, Meiyan Yu, Shougang Chen, Yangtao Zhou, Daoai Wang
, Dalton Trans.
, 2017
, 46
, 10635
- Efficient synthesis of C15 fuel precursor by heterogeneously catalyzed aldol-condensation of furfural with cyclopentanone. Lei Ao, Wei Zhao, Yin-shuang Guan, Ding-kai Wang, Kai-shuai Liu, Tian-tian Guo, Xing Fan, Xian-yong Wei
, RSC Adv.
, 2019
, 9
, 3661
- Solvation spectra. Part 5.—Effect of pressure on the ultra-violet absorption spectrum of solvated iodide. M. J. Blandamer, T. E. Gough, M. C. R. Symons
, Trans. Faraday Soc.
, 1963
, 59
, 1748
- Alkyloxy modified pyrene fluorophores with tunable photophysical and crystalline properties. Andreas Kapf, Hassan Eslahi, Meik Blanke, Marco Saccone, Michael Giese, Marcel Albrecht
, New J. Chem.
, 2019
, 43
, 6361
- The synthesis of some thiophenophanes and attempted cyclisations to polycyclic thiophenium salts. R. Morrin Acheson, Gary C. M. Lee
, J. Chem. Soc., Perkin Trans. 1
, 1987
, 2321
- Core-mediated synthesis, growth mechanism and near-infrared luminescence enhancement of α-NaGdF4@β-NaLuF4:Nd3+ core–shell nanocrystals. Qinqin Shao, Chao Yang, Xiaoxu Chen, Hong Zhang, Guoying Feng, Shouhuan Zhou
, CrystEngComm
, 2020
, 22
, 1359
- Synthesis of solandelactone F, constanolactone A and an advanced intermediate towards solandelactone E from a common synthetic intermediate. Raju Yalla, Sadagopan Raghavan
, Org. Biomol. Chem.
, 2019
, 17
, 4572