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排序方式: 共有153条查询结果,搜索用时 125 毫秒
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Deerenberg S Schrekker HS van Strijdonck GP Kamer PC van Leeuwen PW Fraanje J Goubitz K 《The Journal of organic chemistry》2000,65(16):4810-4817
A series of chiral phosphine-phosphite ligands 1-6 have been synthesized and used in the enantioselective palladium-catalyzed reaction of rac-1,3-diphenyl-2-propenyl acetate with dimethyl malonate as nucleophile. Ligands 1a, 2, 3, 5a, 6a, and 6b have been synthesized starting from racemic tert-butylphenylphosphinoborane. The use of dynamically resolved Li phosphide (-)-sparteine provided the optically pure ligands. Crystals of the allylpalladium (6a) complex were obtained, suitable for X-ray crystal structure determination. The X-ray crystal structure of the allylpalladium (6a) complex revealed a longer palladium-carbon bond distance trans to the phosphine moiety indicating that the attack of the nucleophile takes place at the carbon trans to the phosphine moiety. This was confirmed by the fact that the phosphine moiety did not affect the enantioselectivity directly. Under mild reaction conditions, enantioselectivities up to 83% were obtained (25 degrees C) with ligand 1e. Systematic variation of the ligand bridge and the phosphite moiety showed that the configuration of the product is controlled by the atropisomerism of the biphenyl substituent at the phosphite moiety. The conformation of the biphenyl group, in turn, is controlled by the substituent at the chiral carbon in the bridge. Ligands with large bite angles yielded higher enantioselectivities. 相似文献
3.
Yang Shen Ioanna Kalograiaki Alessio Prunotto Matthew Dunne Samy Boulos Nicholas M. I. Taylor Eric T. Sumrall Marcel R. Eugster Rebecca Martin Alicia Julian-Rodero Benjamin Gerber Petr G. Leiman Margarita Menndez Matteo Dal Peraro Francisco Javier Caada Martin J. Loessner 《Chemical science》2021,12(2):576
Endolysins are bacteriophage-encoded peptidoglycan hydrolases targeting the cell wall of host bacteria via their cell wall-binding domains (CBDs). The molecular basis for selective recognition of surface carbohydrate ligands by CBDs remains elusive. Here, we describe, in atomic detail, the interaction between the Listeria phage endolysin domain CBD500 and its cell wall teichoic acid (WTA) ligands. We show that 3′O-acetylated GlcNAc residues integrated into the WTA polymer chain are the key epitope recognized by a CBD binding cavity located at the interface of tandem copies of beta-barrel, pseudo-symmetric SH3b-like repeats. This cavity consists of multiple aromatic residues making extensive interactions with two GlcNAc acetyl groups via hydrogen bonds and van der Waals contacts, while permitting the docking of the diastereomorphic ligands. Our multidisciplinary approach tackled an extremely challenging protein–glycopolymer complex and delineated a previously unknown recognition mechanism by which a phage endolysin specifically recognizes and targets WTA, suggesting an adaptable model for regulation of endolysin specificity.Combining genetic, biochemical and computational approaches, we elucidated the molecular mechanisms underlying the recognition of Listeria wall teichoic acid by bacteriophage-encoded SH3b repeats. 相似文献
4.
Abe K Akagi T Anthony PL Antonov R Arnold RG Averett T Band HR Bauer JM Borel H Bosted PE Breton V Button-Shafer J Chen JP Chupp TE Clendenin J Comptour C Coulter KP Court G Crabb D Daoudi M Day D Dietrich FS Dunne J Dutz H Erbacher R Fellbaum J Feltham A Fonvieille H Frlez E Garvey D Gearhart R Gomez J Grenier P Griffioen KA Hoibraten S Hughes EW Hyde-Wright C Johnson JR Kawall D Klein A Kuhn SE Kuriki M Lindgren R Liu TJ Lombard-Nelsen RM Marroncle J Maruyama T Maruyama XK McCarthy J Meyer W 《Physical review letters》1995,74(3):346-350
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R. S. Dunne A. J. Macfarlane J. A. de Azcárraga J. C. Pérez Bueno 《Czechoslovak Journal of Physics》1996,46(12):1235-1242
Theq-calculus for genericq is developed and related to the deformed oscillator of parameterq
1/2. By passing with care to the limit in whichq is a root of unity, one uncovers the full algebraic structure ofZ
n
-graded fractional supersymmetry and its natural representation.Presented at the 5th International Colloquium on Quantum Groups: Quantum Groups and Integrable Systems, Prague, 20–22 June 1996.This paper describes research supported in part by E.P.S.R.C and P.P.A.R.C. (UK) and by the C.I.C.Y.T (Spain). J.C.P.B. wishes to acknowledge an FPI grant from the CSIC and the Spanish Ministry of Education and Science. 相似文献
7.
Anthony PL Arnold RG Band HR Borel H Bosted PE Breton V Cates GD Chupp TE Dietrich FS Dunne J Erbacher R Fellbaum J Fonvieille H Gearhart R Holmes R Hughes EW Johnson JR Kawall D Keppel C Kuhn SE Lombard-Nelsen RM Marroncle J Maruyama T Meyer W Meziani Z Middleton H Morgenstern J Newbury NR Petratos GG Pitthan R Prepost R Roblin Y Rock SE Rokni SH Shapiro G Smith T Souder PA Spengos M Staley F Stuart LM Szalata ZM Terrien Y Thompson AK White JL Woods M Xu J Young CC Zapalac G 《Physical review D: Particles and fields》1996,54(11):6620-6650
8.
Dunne KS Bisaro F Odell B Paris JM Gouverneur V 《The Journal of organic chemistry》2005,70(26):10803-10809
[reaction: see text] The preparation of phosphorus-containing trienes featuring two diastereotopic vinyl moieties followed by a diastereoselective ring-closing metathesis is described. This methodology allowed for the synthesis of novel highly functionalized P-stereogenic heterocycles featuring both an exo- and an endocyclic double bond. An investigation into the factors influencing the diastereochemical outcome of the ring-closing metathesis is also presented, revealing that the geometry of the double bonds conjugated to phosphorus is important and that 1,3-stereoinduction is superior to 1,4-stereoinduction for these reactions. 相似文献
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