𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Inhibited enzyme electrodes. Part 3: A sensor for low levels of H2S and HCN

✍ Scribed by W. John Albery; Anthony E.G. Cass; Bernard P. Mangold; Zhi Xin Shu

Book ID
103975662
Publisher
Elsevier Science
Year
1990
Tongue
English
Weight
756 KB
Volume
5
Category
Article
ISSN
0956-5663

No coin nor oath required. For personal study only.

πŸ“œ SIMILAR VOLUMES

ChemInform Abstract: Synthesis of Ξ²-Lact
ChemInform Abstract: Synthesis of Ξ²-Lactones. Part 9. Synthesis of Enantiomerically Pure Ξ²-Lactones by the Tandem Aldolβ€”Lactonization. A Highly Efficient Access to (3S,4S)-3-Hexyl-4-[(2S)-2-hydroxytridecyl]oxetan-2-one (IV), the Key Intermediate for the Enzyme Inhibitors Tetrahydrolipstatin (VIa) and Tetrahydroesterastin (VIb).
✍ Christine Wedler; Burckhard Costisella; Hans Schick πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 33 KB πŸ‘ 1 views
ChemInform Abstract: ATP-Citrate Lyase a
ChemInform Abstract: ATP-Citrate Lyase as a Target for Hypolipidemic Intervention. Part 2. Synthesis and Evaluation of (3R*,5S*)-Ο‰-Substituted-3-carboxy-3,5-dihydroxyalkanoic Acids and Their Ξ³-Lactone Prodrugs as Inhibitors of the Enzyme in vitro and in vivo.
✍ A. D. GRIBBLE; ET AL. ET AL. πŸ“‚ Article πŸ“… 2010 πŸ› John Wiley and Sons βš– 34 KB πŸ‘ 2 views

ATP-Citrate Lyase as a Target for Hypolipidemic Intervention. Part 2. Synthesis and Evaluation of (3R\*,5S\*)-Ο‰-Substituted-3carboxy-3,5-dihydroxyalkanoic Acids and Their Ξ³-Lactone Prodrugs as Inhibitors of the Enzyme in vitro and in vivo. -A series of the title compounds is synthesized and evalua

1H-1,3-Diazepines, 5H-1,3-diazepines, 1,
1H-1,3-Diazepines, 5H-1,3-diazepines, 1,3-diazepinones, and 2,4-diazabicyclo[3.2.0]heptenesPreliminary reports on parts of this work have been published in ref 1. This paper is Diazepines, Part 3. For Part 2, see ref 2.,Electronic supplementary information (ESI) available: NMR spectra of 4a, 4c, 19v ? 20, 19a ? 25a, and 19g ? 25g (Fig. S1?S6), Arrhenius and Eyring plots for H-exchange in 4b,c (Fig. S7), views of the X-ray crystal structures of compounds 26 and 22bB (Fig. S8?S9), bond lengths and angles for compounds 4k, 22bB and 26, preparative procedures and characterization data for all compounds not described in the Experimental section, and computational data (Cartesian coordinates, absolute energies, IR, 1H and 13C NMR) for 20a?c, 21a?b, 22aA?F and 22aB dimer. See http://www.rsc.org/suppdata/ob/b3/b317099c/
✍ Reisinger, Ales; Koch, Rainer; Bernhardt, Paul V.; Wentrup, Curt πŸ“‚ Article πŸ“… 2004 πŸ› Royal Society of Chemistry 🌐 English βš– 496 KB