The Armspach Group

Stacks Image 17052
29.
BINOL-derived phosphoramidites in asymmetric hydrogenation: can the presence of a functionality in the amino group influence the catalytic outcome?
L. Eberhardt, D. Armspach, J. Harrowfield, D. Matt,
Chem. Soc. Rev. 2008, 37, 839-864.




Stacks Image 17054
28.
Synthesis and properties of TRANSDIP, a rigid chelator built upon a cyclodextrin cavity. Is TRANSDIP an authentic trans-spanning ligand?
L. Poorters, D. Armspach, D. Matt, L. Toupet, S. Choua, P. Turek,
Chem. Eur. J. 2007, 13, 9448-9461.




Stacks Image 17086
27.
Efficient asymmetric hydrogenation of olefins with hydrazine-derived diphosphoramidites
L. Eberhardt, D. Armspach, D. Matt, B. Oswald, L. Toupet,
Org. Biomol. Chem. 2007, 5, 3340–3346.




26.
Chiral selectors for enantioresolution and quantitation of the antidepressant drug uoxetine in pharmaceutical formulations by
19F NMR spectroscopic method
M. Shamsipur, L. S. Dastjerdi, S. Haghgoo, D. Armspach, D. Matt, H. Y. Aboul-Enein
Anal. Chim. Acta 2007, 601, 130-138.




Stacks Image 17082
25.
Efficient, rhodium-catalyzed hydrogena tion of α-dehydroamino acid esters with chiral monodentate aminophosphanes bearing two binaphthyl groups
L. Eberhardt, D. Armspach, D. Matt, L. Toupet, B. Oswald,
Eur. J. Org. Chem. 2007, 5395-5403.




Stacks Image 17080
24.
α-TEPHOS: A cyclodextrin-derived tetraphosphine for multiple metal binding
L. Poorters, D. Armspach, D. Matt, L. Toupet,
Dalton Trans. 2007, 3195-3202.




Stacks Image 17078
23. Synthesis of chiral, monodentate aminophosphine and phosphoramidite ligands derived from amino acid esters. Application in the Rh-catalysed asymmetric olefin hydrogenation
L. Eberhardt, D. Armspach, D. Matt, L. Toupet, B. Oswald,
Eur. J. Inorg. Chem. 2007, 4153-4161.




Stacks Image 17076
22.
A metallocavitand functioning as a container for anions. Formation of non-covalent, linear assemblies mediated by a cyclodextrin-entrapped NO
3 anion
L. Poorters, D. Armspach, D. Matt, L. Toupet,
Angew. Chem. Int. Ed. 2007, 46, 2663-2665.




21.
Cyclodextrin-based thiacavitands as building blocks for the construction of metallo-nanotubes
D. Armspach, L. Poorters, D. Matt, B. Benmerad, P. Jones, I. Dix, L. Toupet,
J. Incl. Phenom. Macrocycl. Chem, 2007, 57, 243-250.




Stacks Image 17070
20.
Sulfur-capped cyclodextrins: a new class of cavitands with extroverted as well as introverted donor functionalities
B. Benmerad, P. Clair, D. Armspach, D Matt, F. Balegroune, L. Toupet,
Chem. Commun. 2006, 2678-2680.