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396Pieter Levecque, David W. Gammon, Pierre Jacobs, Dirk De Vos and Bert Sels.
The use of ultrastable Y zeolites in the Ferrier rearrangement of acetylated and benzylated glycals, Green Chem., 2010, 12, 828. Ken Motokura, Hirokazu Yoneda, Akimitsu Miyaji and Toshihide Baba.
Catalytic ring-opening allylation of cyclic acetals with allylsilanes using silica-alumina, Green Chem., 2010, 12, 1373. M. Haberecht, H.-W. Lerner and M. Bolte.
p-Bis(trimethylsilyl)benzene: rerefinement against new intensity data, Acta Cryst. (2002). E58, o436-o437Â Â Â Â N. Nagel, M. Ansari and H. Bock.
1,2,4,5-Tetrakis(trimethylsilylmethyl)benzene at 150K, Acta Cryst. (1997). C53, 1329-1331Â Â Â Â Ryosuke Asami, Toshio Fuchigami and Mahito Atobe.
Development of an anodic substitution reaction system using acoustic emulsification, Chem. Commun., 2008, 244. Amos B. Smith, III and William M. Wuest.
Evolution of multi-component anion relay chemistry (ARC): construction of architecturally complex natural and unnatural products, Chem. Commun., 2008, 5883. Cristina E. Petrisor, Luis Manuel Frutos, Obis Castaño, Marta E. G. Mosquera, Eva Royo and Tomás Cuenca.
Olefinisomerisationversushydrozirconation: a case of a stable β-hydrogen-containing Zr-alkyl derivative, Dalton Trans., 2008, 2670. Ryosuke Asami, Toshio Fuchigami and Mahito Atobe.
A new approach to anodic substitution reaction using acoustic emulsification, Org. Biomol. Chem., 2008, 6, 1938. Ken Motokura, Hirokazu Yoneda, Akimitsu Miyaji, Yasuharu Sakamoto and Toshihide Baba.
Catalytic synthesis of homoallyloxyalcohols and 1,2-bis(homoallyloxy)ethanes through ring-opening allylation of cyclic acetals with allylsilanes over solid acids, Catal. Sci. Technol., 2011, 1, 470. Tanmay Chatterjee, Raju Dey and Brindaban C. Ranu.
An easy access to styrenes: trans aryl 1,3-, 1,4- and 1,5-dienes, and 1,3,5-trienes by Hiyama cross-coupling catalyzed by palladium nanoparticles, New J. Chem., 2011, 35, 1103.