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426Sandra Gil, Marta Costas, Franciso Pena, Inmaculada De La Calle, Noelia Cabaleiro, Isela Lavilla and Carlos Bendicho.
On-line UV photoreduction in a flow-injection/stopped-flow manifold for determination of mercury by cold vapour-atomic absorption spectrometry, Anal. Methods, 2010, 2, 1798. M. Selvaraj and P. K. Sinha.
Highly selective and clean synthesis of nopol over well-ordered mesoporous tin silicate catalysts, New J. Chem., 2010, 34, 1921. Shaofeng Shao, Momtchil Dimitrov, Naijia Guan and Ralf Köhn.
Synthesis and characterization of highly organized mesoporous palladium-doped tin dioxide thin films for gas sensing, J. Mater. Chem., 2009, 19, 8411. Anderson S. Ribeiro, Mariana A. Vieira, Patricia Grinberg and Ralph E. Sturgeon.
Vapor generation coupled with furnace atomization plasma emission spectrometry for detection ofmercury, J. Anal. Atom. Spectrosc., 2009, 24, 689. Dorothee Irmgard Fried, Alesja Ivanova, Vesna Müller, Jiri Rathousky, Bernd M. Smarsly and Dina Fattakhova-Rohlfing.
A facile synthesis of mesoporous crystalline tin oxide films involving a base-triggered formation of sol–gel building blocks, Nanoscale, 2011, 3, 1234. John S. Carey, Somhairle MacCormick, Steven J. Stanway, Aphiwat Teerawutgulrag and Eric J. Thomas.
Effective 1,5-, 1,6- and 1,7-remote stereocontrol in reactions of alkoxy- and hydroxy-substituted allylstannanes with aldehydes, Org. Biomol. Chem., 2011, 9, 3896. Jamie F. Bickley, Adam T. Gillmore, Stanley M. Roberts, John Skidmore and Alexander Steiner.
Synthesis and reactions of some optically active epoxides formally derived from tertiary allylic alcohols, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 1109. Dan Farcasiu, Rodica Leu and Paula J. Ream.
The 1?:?1 and 2?:?1 complexes of diethyl ether with tin tetrachloride and their stability, studied by Sn NMR spectroscopy, J. Chem. Soc., Perkin Trans. 2, 2001, 0, 427. David J. Hallett, Nongluk Tanikkul and Eric J. Thomas.
Remote stereocontrol in reactions between 4- and 5-alkoxyalk-2-enylstannanes and 1-alkoxycarbonylimines and analogues: stereoselective approaches to novel a-amino acids, Org. Biomol. Chem., 2012, 10, 6130.