Competitive formation of homocircuit [3]rotaxanes in synthetically useful yields in the bipyridine-mediated active template CuAAC reaction† †Electronic supplementary information (ESI) available: Full experimental details and characterisation of all novel compounds. See DOI: 10.1039/c4sc03999h Click here for additional data file.
نویسندگان
چکیده
منابع مشابه
Exploiting recognition-mediated assembly and reactivity in [2]rotaxane formation† †Electronic supplementary information (ESI) available: Details of kinetic experiments, computational methods and characterisation data for all compounds are provided. See DOI: 10.1039/c5sc04805b Click here for additional data file.
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Facile synthesis of oligoyne amphiphiles and their rotaxanes† †Electronic supplementary information (ESI) available: Fig. S1–S4 and a comprehensive account of all experimental details, including synthetic procedures, analytical data, and NMR spectra of all novel compounds. See DOI: 10.1039/c4sc03154g Click here for additional data file.
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Synthesis and stabilities of peptide-based [1]rotaxanes: molecular grafting onto lasso peptide scaffolds† †Electronic supplementary information (ESI) available: Experimental procedures and analytical data of all new compounds. CCDC 1520783. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc00021a Click here for additional data file. Click here for additional data file.
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Novel octavalent cross-linker displays efficient trapping of protein–protein interactions† †Electronic supplementary information (ESI) available: General experimental details and characterisation data for compounds 1–3. See DOI: 10.1039/b701542a Click here for additional data file. Click here for additional data file.
A novel octavalent, resorcin[4]arene derived, cross-linker designed to overcome some of the limitations of commercially available reagents is significantly more efficient for covalent stabilisation of protein-protein interactions.
متن کاملPhotoswitchable interlocked thiodiglycolamide as a cocatalyst of a chalcogeno-Baylis–Hillman reaction† †Electronic supplementary information (ESI) available: Experimental procedures, spectroscopic and mass spectrometry data for all of the new compounds, and the full crystallographic details of 3a. CCDC 1532346. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c7sc00724h Click here for additional data file. Click here for additional data file.
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عنوان ژورنال:
دوره 6 شماره
صفحات -
تاریخ انتشار 2015