Protocol for the purification of protected carbohydrates: toward coupling automated synthesis to alternate-pump recycling high-performance liquid chromatography† †Electronic supplementary information (ESI) available: Additional figures and characterization of final compound. See DOI: 10.1039/c6cc07584c Click here for additional data file.

Dynamic induction of enantiomeric excess from a prochiral azobenzene dimer under circularly polarized light† †Electronic supplementary information (ESI) available: Synthesis, 1H NMR spectra, 13C NMR spectra, UV absorption plots, HPLC traces, and CD spectra of the compounds; crystallographic information files. CCDC 1003754. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c4sc01993h Click here for additional data file. Click here for additional data file.

An unprecedented amplification of near-infrared emission in a Bodipy derived π-system by stress or gelation† †Electronic supplementary information (ESI) available: Experimental details, synthesis procedures and characterization data of the compounds, and additional figures. CCDC 1523313. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc01696d Click here for additional data file. Click here for additional data file.

Automated synthesis of backbone protected peptides† †Electronic supplementary information (ESI) available: Synthesis and characterization of peptides, experimental conditions. See DOI: 10.1039/c4cc03065f Click here for additional data file.

The synthesis of peptides rich in aggregation prone sequences can be improved with backbone protection. We report the automated introduction of backbone protection to a peptide. This new method was applied in a fully-automated synthesis, giving improved handling, quality and yield of several challenging target sequences.

Photoacoustic probes for real-time tracking of endogenous H2S in living mice† †Electronic supplementary information (ESI) available: Procedures for the synthesis of BODPA, living mice imaging, characterization data, and supplementary figures. See DOI: 10.1039/c6sc04703c Click here for additional data file.

Unified synthesis of mono/bis-arylated phenols via RhIII-catalyzed dehydrogenative coupling† †Electronic supplementary information (ESI) available: Experimental procedures and characterization data for all new compounds. CCDC 1047606, 1426755, 1438599 and 1442845. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6sc03169b Click here for additional data file. Click here for additional data file.