Search Results - "Croft, A K"

Controlling the action of chlorine radical: from lab to environment by Croft, A K, Howard-Jones, H M, Skates, C E, Wood, C C

“…The strength of Bz-Cl˙ complexation has been explored using density functional theory (DFT) calculations, including dispersion-corrected (DFT-D) calculations…”
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Proline-rich proteins--deriving a basis for residue-based selectivity in polyphenolic binding by Croft, A K, Foley, M K

“…(1)H NMR titration experiments have been used to establish that minimal proline-based models show enhanced binding selectivity towards phenol in CDCl(3),…”
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Recent advances in the use of ionic liquids as solvents for protein-based materials and chemistry by Hagen, M.L., Harper, J.B., Croft, A.K.

“…Proteins are a diverse class of molecules that can act as catalysts and structural components. Interest in their interactions with ionic solvents is on the…”
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Ethyl Diazoacetate in Catalytic Reactions with Imides: Experimental and Calculation Data by Nikolaev, Vs. V., Hennig, L., Croft, A. K., Schulze, B., Kostikov, R. R., Nikolaev, V. A.

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Design of Radical-Resistant Amino Acid Residues:  A Combined Theoretical and Experimental Investigation by Croft, Anna K, Easton, Christopher J, Radom, Leo

“…Ab initio calculations have been used to design radical-resistant amino acid residues. Optimized structures of free and protected amino acids and their…”
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Strategic use of amino acid N-substituents to limit α-carbon-centered radical formation and consequent loss of stereochemical integrity by Croft, Anna K., Easton, Christopher J., Kociuba, Katherine, Radom, Leo

“…Ab initio calculations have been used to investigate the effect of N-substituents on the stability of α-carbon-centered amino acid radicals. Optimized…”
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Stereocontrol in ene-dimerisation and trimerisation of 1-trimethylsilyl-3-phenylcyclopropene by Sheshenev, Andrey E., Baird, Mark S., Croft, Anna K., Starikova, Zoya A., Shashkov, Alexandre S., Zhuze, Alexey L., Bolesov, Ivan G.

“…1-Trimethylsilyl-3-phenylcyclopropene undergoes a highly stereocontrolled ene-reaction to give a dimer and further reaction leads to one or more trimers…”
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Generation and stereocontrolled trapping of 3-phenylcyclopropene and its derivatives by Sheshenev, Andrey E., Baird, Mark S., Croft, Anna K., Bolesov, Ivan G.

“…Selective methods for the preparation of 3-phenylcyclopropene and its 1-substituted derivatives are provided. The parent cyclopropene is readily trapped in…”
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