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- 1-Phenyl-1H-pyrrole-2,5-dicarboxylic acid derivatives as
versatile hydrogen-bonding motifs for the formation of one-, two- and
three-dimensional networks in the solid state †. Qing Lin, Steven J. Geib, Andrew D. Hamilton
, J. Chem. Soc., Perkin Trans. 2
, 1998
, 2109
- Further insight into the coordination of 2,5-dicarbothioamidopyrroles: the case of Cu and Co complexes. Louise E. Karagiannidis, Philip A. Gale, Mark E. Light, Massimiliano Massi, Mark I. Ogden
, Dalton Trans.
, 2011
, 40
, 12097
- Structural diversity in the first metal complexes of 2,5-dicarboxamidopyrroles and 2,5-dicarbothioamidopyrroles. Gareth W. Bates, Philip A. Gale, Mark E. Light, Mark I. Ogden, Colin N. Warriner
, Dalton Trans.
, 2008
, 4106
- Solution and solid-state studies of 3,4-dichloro-2,5-diamidopyrroles: formation of an unusual anionic narcissistic dimer. Salvatore Camiolo, Philip A. Gale, Michael B. Hursthouse, Mark E. Light, Andy J. Shi
, Chem. Commun.
, 2002
, 758
- Pyrrolylamidourea based anion receptors. Louise S. Evans, Philip A. Gale, Mark E. Light, Roberto Quesada
, New J. Chem.
, 2006
, 30
, 1019
- Nitrophenyl derivatives of pyrrole 2,5-diamides: structural behaviour, anion binding and colour change signalled deprotonation. Salvatore Camiolo, Philip A. Gale, Michael B. Hursthouse, Mark E. Light
, Org. Biomol. Chem.
, 2003
, 1
, 741
- Index of subjects
, J. Chem. Soc., Abstr.
, 1911
, 100
, ii1297
- Actinomycetes: still a source of novel antibiotics. Olga Genilloud
, Nat. Prod. Rep.
, 2017
, 34
, 1203
- Unexpected stable dimerisation of an anionic imidopyrrolecarboxylate in polar solution. Carolin Rether, Elisabeth Verheggen, Carsten Schmuck
, Chem. Commun.
, 2011
, 47
, 9078
- Amidopyrroles: from anion receptors to membrane transport agents. Philip A. Gale
, Chem. Commun.
, 2005
, 3761