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19Ashutosh Banerjee, Roland Fröhlich, Dirk Schepmann and Bernhard Wünsch.
Synthesis and NMDA receptor affinity of dexoxadrol analogues with modifications in position 4 of the piperidine ring, Med. Chem. Commun., 2010, 1, 87. Marek Jura, William Levason, Gillian Reid and Michael Webster.
Preparation and properties of sterically demanding and chiral distibine ligands, Dalton Trans., 2008, 5774. Ghenia Bentabed-Ababsa, Aicha Derdour, Thierry Roisnel, Jose A. Sáez, Luis R. Domingo and Florence Mongin.
Polar [3 + 2] cycloaddition of ketones with electrophilically activated carbonyl ylides. Synthesis of spirocyclic dioxolane indolinones, Org. Biomol. Chem., 2008, 6, 3144. Stephen G. Davies, Matthew J. Durbin, Euan C. Goddard, Peter M. Kelly, Wataru Kurosawa, James A. Lee, Rebecca L. Nicholson, Paul D. Price, Paul M. Roberts, Angela J. Russell, Philip M. Scott and Andrew D. Smith.
Doubly diastereoselective conjugate addition of homochiral lithium amides to homochiral α,β-unsaturated esters containing cis- and trans-dioxolane units, Org. Biomol. Chem., 2009, 7, 761. Avelina Arnanz, Camino González-Arellano, Alberto Juan, Gonzalo Villaverde, Avelino Corma, Marta Iglesias and Félix Sánchez.
New chiral ligands bearing two N-heterocyclic carbene moieties at a dioxolane backbone. Gold, palladium and rhodium complexes as enantioselective catalysts, Chem. Commun., 2010, 46, 3001. Sara Dolci, Fabio MarchettiBorn in Bologna (Italy) in 1974., Guido Pampaloni and Stefano Zacchini.
A systematic study on the activation of simple polyethers by MoCl5 and WCl6, Dalton Trans., 2010, 39, 5367. Thomas Jozak, Yu Sun and Werner R. Thiel.
Synthesis, characterization and co-ordination chemistry of dioxolanedipyrazoles, New J. Chem., 2011, 35, 2114. Stephen G. Davies, Emma M. Foster, Aileen B. Frost, James A. Lee, Paul M. Roberts and James E. Thomson.
On the origins of diastereoselectivity in the conjugate additions of the antipodes of lithium N-benzyl-(N-a-methylbenzyl)amide to enantiopure cis- and trans-dioxolane containing a,ß-unsaturated est
ers, Org. Biomol. Chem., 2012, 10, 6186. Introduction, Total Synthesis of Plakortide E and Biomimetic Synthesis of Plakortone B Results and Discussion, Total Synthesis of Plakortide E and Biomimetic Synthesis of Plakortone B