Results
1 -
10 of
440Benito Alcaide, Pedro Almendros and Cristina Aragoncillo.
Exploiting [2+2] cycloaddition chemistry: achievements with allenes, Chem. Soc. Rev., 2010, 39, 783. Antonio Antiñolo, Santiago García-Yuste, Isabel Lopez Solera, Antonio Otero, Juan Carlos Pérez-Flores, Rebeca Reguillo-Carmona, Elena Villaseñor, Eva Santos, Erik Zuidema and Carles Bo.
Reactions of alkynes with phosphido niobocenes: a combined experimental and theoretical study, Dalton Trans., 2010, 39, 1962. Stephen R. D. George, Gavin L. Edwards and Jason B. Harper.
The effects of ionic liquids on azide-alkyne cycloaddition reactions, Org. Biomol. Chem., 2010, 8, 5354. Mamoru Yamaguchi, Yasuhiro Arikawa, Yoshimasa Nishimura, Keisuke Umakoshi and Masayoshi Onishi.
Vinylidene
rutheniums with an electrostructurally-flexible NO ligand and their ruthenacyclobutene formation, Chem. Commun., 2009, 2911. Alina M. Balu, Simon B. Duckett and Rafael Luque.
Para-hydrogen induced polarisation effects in liquid phase hydrogenations catalysed by supported metal nanoparticles, Dalton Trans., 2009, 5074. Alana E. C. Collis and István T. Horváth.
Heterogenization of homogeneous catalytic systems, Catal. Sci. Technol., 2011, 1, 912. Garima Choudhary and Rama Krishna Peddinti.
Introduction of a clean and promising protocol for the synthesis of β-amino-acrylates and 1,4-benzoheterocycles: an emerging innovation, Green Chem., 2011, 13, 3290. Frances Heaney, Julie Fenlon, Colm O'Mahony, Patrick McArdle and Desmond Cunningham.
Nitrogen-containing heterocycles: 1,3-dipolar cycloaddition of stabilized nitrones with alkynes; primary cycloadducts, first and second generation rearrangement processes, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 3382. Max Herberhold, Hong Yan, Wolfgang Milius and Bernd Wrackmeyer.
Selective stepwise carborane substitution in B(3,6) positions in Cp*Ir half-sandwich complexes containing a chelating 1,2-dicarba-closo-dodecaborane-1,2-dichalcogenolato ligand, Dalton Trans., 2001, 0, 1782. Richard N. Butler and Anthony Fox.
Transformations of selenadiazoliumyl-N-unsubstituted methanides (ylides) to new divinyl selenide derivatives and substituted 1,3,5-selenadiazines. Organoselenium systems from azolium 1,3-dipoles, J. Chem. Soc., Perkin Trans. 1, 2001, 0, 394.