Recognition properties of receptors consisting of imidazole and indole recognition units towards carbohydrates

• Monika Mazik and
• André Hartmann

Beilstein J. Org. Chem. 2010, 6, No. 9, doi:10.3762/bjoc.6.9

• equiv of the receptor, indicating important contribution of the OH groups of 6a to the complex formation. Furthermore, the addition of 4 or 5 to a CDCl3 solution of β-glucoside 6a caused significant upfield shift of the CH signals of 6a, indicating the participation of the sugar CH units in the

An enantiomerically pure siderophore type ligand for the diastereoselective 1 : 1 complexation of lanthanide(III) ions

• Markus Albrecht,
• Olga Osetska,
• Thomas Abel,
• Gebhard Haberhauer and
• Eva Ziegler

Beilstein J. Org. Chem. 2009, 5, No. 78, doi:10.3762/bjoc.5.78

• facile synthesis of a highly preorganized tripodal enterobactine-type ligand 1a-H3 consisting of a chiral C3-symmetric macrocyclic peptide and three tridentate 2-amido-8-hydroxyquinoline coordinating units is presented. Complex formation with various metal ions (Al3+, Ga3+, Fe3+, La3+ and Eu3+) was

• described dissociation equilibrium in solution uncoordinated ligand can be observed as well at m/z = 1464.9 {K(1a-H3)}+. UV and CD titration experiments As a sensitive technique for the investigation of the complex formation of ligand 1a-H3 with a series of trivalent metal ions we performed UV–vis as well

• simplification reduces the number of optimization steps in the calculations and should not affect the extent of diastereoselectivity for the complex formation. In principle the C3-symmetric 1b·La complex can adopt four different conformations (Λ1, Λ2, Δ1, Δ2): The 8-hydroxyquinoline units can be present in two

An efficient synthesis of novel pyrano[2,3-d]- and furopyrano[2,3-d]pyrimidines via indium- catalyzed multi- component domino reaction

• Dipak Prajapati and
• Mukut Gohain

Beilstein J. Org. Chem. 2006, 2, No. 11, doi:10.1186/1860-5397-2-11

• %). Introduction The emergence of indium(III) compounds as efficient Lewis acid catalysts presents new and exciting opportunities for organoindium chemistry. [1][2] It was found that the low reactivity of trivalent organoindium reagents can be increased by complex formation with organolithium compounds.[3] The