Artificial metalloenzymes for olefin metathesis based on the biotin-(strept)avidin technology.
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Thomas R Ward | David Gnandt | M. Ringenberg | T. Ward | Yvonne M. Wilson | David Gnandt | Mark R Ringenberg | Cheikh Lo | Yvonne Wilson | Y. Wilson | Cheikh Lo
[1] Tillmann Heinisch,et al. Design strategies for the creation of artificial metalloenzymes. , 2010, Current opinion in chemical biology.
[2] A. Kirschning,et al. Sustainable concepts in olefin metathesis. , 2007, Angewandte Chemie.
[3] N. Green. [74] Spectrophotometric determination of avidin and biotin , 1970 .
[4] Thomas R Ward,et al. Artificial metalloenzymes based on the biotin-avidin technology: enantioselective catalysis and beyond. , 2011, Accounts of chemical research.
[5] M. Francis,et al. Optimization of a biomimetic transamination reaction. , 2008, Journal of the American Chemical Society.
[6] M. Reetz. Directed Evolution of Stereoselective Hybrid Catalysts , 2009 .
[7] A. Hoveyda,et al. The remarkable metal-catalysed olefin metathesis reaction , 2007, Nature.
[8] Marjana Novic,et al. (Strept)avidin as host for biotinylated coordination complexes: stability, chiral discrimination, and cooperativity. , 2006, Inorganic chemistry.
[9] H. Gampp,et al. Calculation of equilibrium constants from multiwavelength spectroscopic data-I Mathematical considerations. , 1985, Talanta.
[10] A. Zocchi,et al. Artificial metalloenzymes: (strept)avidin as host for enantioselective hydrogenation by achiral biotinylated rhodium-diphosphine complexes. , 2004, Journal of the American Chemical Society.
[11] M. Francis,et al. Chemoselective tryptophan labeling with rhodium carbenoids at mild pH. , 2009, Journal of the American Chemical Society.
[12] H. Gampp,et al. Calculation of equilibrium constants from multiwavelength spectroscopic data--II: SPECFIT: two user-friendly programs in basic and standard FORTRAN 77. , 1985, Talanta.
[13] Carolyn R Bertozzi,et al. Bioorthogonal chemistry: fishing for selectivity in a sea of functionality. , 2009, Angewandte Chemie.
[14] M. Distefano,et al. Generation of new enzymes via covalent modification of existing proteins. , 2001, Chemical reviews.
[15] K. Grela,et al. Ruthenium-based olefin metathesis catalysts bearing N-heterocyclic carbene ligands. , 2009, Chemical reviews.
[16] J. Kirsch,et al. A sensitive fluorometric assay for avidin and biotin. , 1977, Analytical biochemistry.
[17] B. G. Davis,et al. Olefin Metathesis for Site‐Selective Protein Modification , 2009, Chembiochem : a European journal of chemical biology.
[18] Jason P. Jordan,et al. Small-molecule N-heterocyclic-carbene-containing olefin-metathesis catalysts for use in water. , 2007, Angewandte Chemie.
[19] M. Francis,et al. Tyrosine-selective protein alkylation using pi-allylpalladium complexes. , 2006, Journal of the American Chemical Society.
[20] H. Gampp,et al. Calculation of equilibrium constants from multiwavelength spectroscopic data-III Model-free analysis of spectrophotometric and ESR titrations. , 1985, Talanta.
[21] Yi Lu,et al. Design of functional metalloproteins , 2009, Nature.
[22] K. Grela,et al. Aqueous olefin metathesis. , 2009, Angewandte Chemie.
[23] R. Grubbs,et al. Ruthenium-based heterocyclic carbene-coordinated olefin metathesis catalysts. , 2010, Chemical reviews.
[24] Z. Ball,et al. Structure-selective modification of aromatic side chains with dirhodium metallopeptide catalysts. , 2010, Journal of the American Chemical Society.
[25] B. G. Davis,et al. Allyl sulfides are privileged substrates in aqueous cross-metathesis: application to site-selective protein modification. , 2008, Journal of the American Chemical Society.
[26] B. G. Davis,et al. A convenient catalyst for aqueous and protein Suzuki-Miyaura cross-coupling. , 2009, Journal of the American Chemical Society.
[27] B. G. Davis,et al. Olefin cross-metathesis on proteins: investigation of allylic chalcogen effects and guiding principles in metathesis partner selection. , 2010, Journal of the American Chemical Society.
[28] Gerard Roelfes,et al. DNA-based asymmetric catalysis. , 2010, Chemical Society reviews.