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246Abdoulaye Gassama, Cédric Ernenwein and Norbert Hoffmann.
Synthesis of surfactants from furfural derived 2[5H]-furanone, Green Chem., 2010, 12, 859. M. MartÃnez-Palau, J. PuiggalÃ, X. Solans and L. UrpÃ.
Butane-1,4-diyl bis(bromoacetate), Acta Cryst. (2005). E61, o1028-o1031Â Â Â Â Chao Guo Yan, Xiao Kai Song, Qi Fang Wang, Jing Sun, Ulrich Siemeling and Clemens Bruhn.
One-step synthesis of polysubstituted benzene derivatives by multi-component cyclization of α-bromoacetate, malononitrile and aromatic aldehydes, Chem. Commun., 2008, 1440. Yu Sung Chun, Ki Kon Lee, Young Ok Ko, Hyunik Shin and Sang-gi Lee.
The first chemoselective tandem acylation of the Blaise reaction intermediate: a novel method for the synthesis of α-acyl-β-enamino esters, key intermediate for pyrazoles, Chem. Commun., 2008, 5098. Jitendra R. Harjani, Robert D. Singer, M. Teresa Garcia and Peter J. Scammells.
The design and synthesis of biodegradable pyridinium ionic liquids, Green Chem., 2008, 10, 436. Giona Kilcher, Daniela Delneri, Craig Duckham and Nicola Tirelli.
Probing (macro)molecular transport through cell walls, Faraday Discuss., 2008, 139, 199. Ivan I. Stoikov, Alena A. Yantemirova, Roman V. Nosov, Ildar Kh. Rizvanov, Ajdar R. Julmetov, Vladimir V. Klochkov, Igor S. Antipin, Alexander I. Konovalov and Ilya Zharov.
p-tert-Butyl thiacalix[4]arenes functionalized at the lower rim by amide, hydroxyl and ester groups as anion receptors, Org. Biomol. Chem., 2011, 9, 3225. Toni Moragas Solá, Ian Churcher, William Lewis and Robert A. Stockman.
Stereoselective aza-Darzens reactions of tert-butanesulfinimines: convenient access to chiral aziridines, Org. Biomol. Chem., 2011, 9, 5034. Muhammad Ashram, Shehadeh Mizyed and Paris E. Georghiou.
Ester derivatives of hexahomotrioxacalix[3]naphthalenes: conformational and binding properties with alkali metal cations, Org. Biomol. Chem., 2003, 1, 599. Lassaad Baklouti, Jamila Cherif, Rym Abidi, Françoise Arnaud-Neu, Jack Harrowfield and Jacques Vicens.
Synthesis and binding properties of calix[4]arenes with [2 + 2′] mixed ligating functional groups, Org. Biomol. Chem., 2004, 2, 2786.