Eliminating caspase-7 and cathepsin B cross-reactivity on fluorogenic caspase-3 substrates† †Electronic supplementary information (ESI) available: Supporting figures, synthesis and characterisation of the substrates, and enzymatic assays. See DOI: 10.1039/c5mb00730e Click here for additional data file.

Neutral iodotriazoles as scaffolds for stable halogen-bonded assemblies in solution† †Electronic supplementary information (ESI) available: Details of computational methods, synthesis and characterisation data for all compounds are provided. CCDC 1442418–1442421. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc01974a Click here for additional data file.

School of Chemistry and EaStCHEM, Un Andrews, Fife KY16 9ST, UK. E-mail: d.ph 463808; Tel: +44 (0)1334 467264 Institut de Génétique et de Biologie Molécu UMR 7104, Université de Strasbourg, Graffenstaden, France † Electronic supplementary information ( methods, synthesis and characterisation CCDC 1442418–1442421. For ESI and c electronic format see DOI: 10.1039/c6sc01 Cite this: Chem. Sci., 201...

One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides† †Electronic supplementary information (ESI) available: Experimental details and supporting characterisation data. See DOI: 10.1039/c6sc03924c Click here for additional data file.

Enantioselective Narasaka–Heck cyclizations: synthesis of tetrasubstituted nitrogen-bearing stereocenters† †Electronic supplementary information (ESI) available: Experimental procedures and characterisation data for all compounds are provided. CCDC 1438659 and 1438660. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc04466b Click here for additional data file. Click here for additional data file.

School of Chemistry, University of Bristol, B bris.ac.uk AstraZeneca, Alderley Park, Maccleseld, C AstraZeneca, Pepparedsleden 1, Mölndal, 4 † Electronic supplementary information ( and characterisation data for all compou 1438660. For ESI and crystallographic dat DOI: 10.1039/c6sc04466b ‡ These authors contributed equally. § Author to whom correspondence shou structures of 3b and Pd[(Sa,S)-L-...

pH controlled assembly of a self-complementary halogen-bonded dimer† †Electronic supplementary information (ESI) available: Details of computational methods, synthesis and characterisation data for all compounds are provided. CCDC 1488032–1488035. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03696a Click here for additional data file. Click here for additional data file.

Au(iii)-aryl intermediates in oxidant-free C–N and C–O cross-coupling catalysis† †Electronic supplementary information (ESI) available: Detailed synthesis and full characterization of substrates, products and complexes. Crystallographic data for compounds 1ah, 3a and 3b. CCDC 1489676, 1489681 and 1489682, respectively. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03699f Click here for additional data file. Click here for additional data file.

QBIS-CAT Group, Institut de Qúımica Comp de Qúımica, Universitat de Girona, Campu Spain. E-mail: [email protected] Servei de RMN, Facultat de Cien ̀cies, Univ UAB, Bellaterra E-08193, Catalonia, Spain † Electronic supplementary information full characterization of substrates, prod data for compounds 1ah, 3a and 3b. C respectively. For ESI and crystallographic see DOI: 10.1039/c6sc03699f Cite th...