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18Antonio Otero, Agustín Lara-Sánchez, Juan Fernández-Baeza, Emilia Martínez-Caballero, Isabel Márquez-Segovia, Carlos Alonso-Moreno, Luis F. Sánchez-Barba, Ana M. Rodríguez and Isabel López -Solera.
New achiral and chiral NNE heteroscorpionate ligands. Synthesis of homoleptic lithium complexes as well as halide and alkyl scandium and yttrium complexes, Dalton Trans., 2010, 39, 930. Junpei Kuwabara, Goro Munezawa, Ken Okamoto and Takaki Kanbara.
Palladium(ii) and platinum(ii)SCS pincer ligand with an azulene unit, Dalton Trans., 2010, 39, 6255. Frank Erdmann and Yixin Zhang.
Reversible photoswitching of protein function, Mol. Biosyst., 2010, 6, 2103. Hadi D. Arman, Rebecca L. Gieseking, Timothy W. Hanks and William T. Pennington.
Complementary halogen and hydrogen bonding: sulfur⋯iodine interactions and thioamide ribbons, Chem. Commun., 2010, 46, 1854. Michal Szostak and Jeffrey Aubé.
Synthesis and rearrangement of a bridged thioamide, Chem. Commun., 2009,
, 7122. Gareth W. Bates, Philip A. Gale, Mark E. Light, Mark I. Ogden and Colin N. Warriner.
Structural diversity in the first metal complexes of 2,5-dicarboxamidopyrroles and 2,5-dicarbothioamidopyrroles, Dalton Trans., 2008, 4106. Ahmad Basheer and Zvi Rappoport.
Enols and thioenols of substituted cyanomonothiocarbonylmalonamides: structures, enolizationvs. thioenolization, equilibria and conformations, Org. Biomol. Chem., 2008, 6, 1071. Maria Altamura, Paolo Dapporto, Antonio Guidi, Nicholas J. S. Harmat, Loïc Jierry, Elisa Libralesso, Paola Paoli and Patrizia Rossi.
Investigation on the flexibility of chiral tricyclic derivatives, New J. Chem., 2008, 32, 1617. Bernard Omondi, Andreas Lemmerer, Manuel A. Fernandes, Demetrius C. Levendis and Marcus Layh.
The influence of substitution and weak interactions on the crystal structures of a series of 2,6-disubstituted N-arylthioamides, CrystEngComm, 2009, 11, 1658. Weiying Lin, Xiaowei Cao, Yundi Ding, Lin Yuan and Lingliang Long.
A highly selective and sensitive fluorescent probe for Hg2+ imaging in live cells based on a rhodamine–thioamide–alkyne scaffold, Chem. Commun., 2010, 46, 3529.