Crystal engineering of novel cocrystals of a triazole drug with 1,4-dicarboxylic acids.

By J. Remenar, S. Morissette, M. Peterson, B. Moulton, J. MacPhee, Hector Guzmán, Ö. Almarsson. Journal of the American Chemical Society, 2003

598 citations recorded by the source corpus.

Subfields: Materials Chemistry, Molecular Biology, Physical and Theoretical Chemistry

View Paper: https://www.semanticscholar.org/paper/f7fe641f6fb6769fa38291594d8aa9dedef78ffe

How researchers see this paper

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In Materials Chemistry

1. Christopher J. H. Porter
2. W. Charman
3. S. Charman
4. H. Williams
5. R. Shanker
6. Natalie L. Trevaskis
7. Colin W. Pouton

In Molecular Biology

1. W. Charman
2. Colin W. Pouton
3. Christopher J. H. Porter
4. S. Charman
5. H. Williams
6. R. Shanker
7. Natalie L. Trevaskis

Citations in the corpus

• Strategies to Address Low Drug Solubility in Discovery and Development (2013, background): “Salts formed using strongly acidic or basic counterions typically show a greater inclination to higher crystallinity (Hirsch et al., 1978; Bastin et al., 2000; Remenar et al., 2003a; Black et al., 2007; Gross et al., 2007).”