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- Ecotoxicological assessment of biomass-derived furan platform chemicals using aquatic and terrestrial bioassays. Stella Parmaki, Marlen I. Vasquez, Maria Patsalou, Rafael F. A. Gomes, Svilen P. Simeonov, Carlos A. M. Afonso, Michalis Koutinas
, Environ. Sci.: Processes Impacts
, 2024
, 26
, 686
- Characterization of grape seed residues from the ethanol-distillation industry. Ángela Peralbo-Molina, Feliciano Priego-Capote, María Dolores Luque de Castro
, Anal. Methods
, 2013
, 5
, 1922
- A diketopyrrolopyrrole molecule end-capped with a furan-2-carboxylate moiety: the planarity of molecular geometry and photovoltaic properties. Lei Fu, Weifei Fu, Pei Cheng, Zhixin Xie, Congcheng Fan, Minmin Shi, Jun Ling, Jianhui Hou, Xiaowei Zhan, Hongzheng Chen
, J. Mater. Chem. A
, 2014
, 2
, 6589
- An innovative catalytic pathway for the synthesis of acyl furans: the cross-ketonization of methyl 2-furoate with carboxylic acids. Jacopo De Maron, Davide Cesari, Sabra Banu Rameesdeen, Tommaso Tabanelli, Andrea Fasolini, Francesco Basile, Fabrizio Cavani
, Green Chem.
, 2023
, 25
, 7381
- Selective chemical adsorption of Cd(ii) on silica covalently decorated with a β-ketoenol-thiophene-furan receptor. Said Tighadouini, Smaail Radi, Yann Garcia
, Mol. Syst. Des. Eng.
, 2020
, 5
, 1037
- Infrared examination of rotational isomerism in alkyl furan-2-carboxylates : determination of thermodynamic parameters from infrared data. Derek J. Chadwick, John Chambers, Robert Macrae, G. Denis Meakins, Roger L. Snowden
, J. Chem. Soc., Perkin Trans. 2
, 1976
, 597
- Reductive silylation reactions of ethyl 2-furoates. Isao Kuwajima, Kunio Atsumi, Ichiro Azegami
, J. Chem. Soc., Chem. Commun.
, 1977
, 76
- UV/vis absorption and fluorescence spectroscopic study of some new 4-hydroxy-7-methoxycoumarin derivatives. Part I: Effect of substitution by a benzo-1,4-dioxanyl or an ethyl furoate group in the 3-position. Re′gine Dondon, Vladimir P. Khilya, Alexander D. Roshal, Suzanne Fery-Forgues
, New J. Chem.
, 1999
, 23
, 923
- Synthetic strategy and structure–activity relationship (SAR) studies of 3-(5′-hydroxymethyl-2′-furyl)-1-benzyl indazole (YC-1, Lificiguat): a review. Ko-Hua Yu, Hsin-Yi Hung
, RSC Adv.
, 2022
, 12
, 251
- Instances of non-electrolyte solvation leading to less pronounced rate enhancements of ester hydrolyses in dipolar aprotic solvents: the possibility of hydrolysis via conjugate base formation in the case of ethyl indole-2-carboxylate and methyl 4-pyridylacetate. G. Venkoba Rao, M. Balakrishnan, N. Venkatasubramanian, P. V. Subramanian, V. Subramanian
, J. Chem. Soc., Perkin Trans. 2
, 1978
, 8