22 results on '"Parella, Teodor"'
Search Results
2. Synthesis of C60/[10]CPP‐Catenanes by Regioselective, Nanocapsule‐Templated Bingel Bis‐Addition.
3. Simultaneous Enantiospecific Detection of Multiple Compounds in Mixtures using NMR Spectroscopy
4. Electrophilic Iron Catalyst Paired with a Lithium Cation Enables Selective Functionalization of Non‐Activated Aliphatic C−H Bonds via Metallocarbene Intermediates
5. Cover Picture: Nucleophile Promiscuity of Engineered Class II Pyruvate Aldolase YfaU from E. Coli (Angew. Chem. Int. Ed. 14/2018)
6. Nucleophile Promiscuity of Engineered Class II Pyruvate Aldolase YfaU from E. Coli
7. Intramolecular Benzoin Reaction Catalyzed by Benzaldehyde Lyase from Pseudomonas Fluorescens Biovar I
8. Nucleophile Promiscuity of Engineered Class II Pyruvate Aldolase YfaU from <italic>E. Coli</italic>.
9. Homodecoupled 1,1- and 1,n-ADEQUATE: Pivotal NMR Experiments for the Structure Revision of Cryptospirolepine
10. EngineeredL-Serine Hydroxymethyltransferase fromStreptococcus thermophilusfor the Synthesis of α,α-Dialkyl-α-Amino Acids
11. Pure In-Phase Heteronuclear Correlation NMR Experiments
12. A Definitive NMR Solution for a Simple and Accurate Measurement of the Magnitude and the Sign of Small Heteronuclear Coupling Constants on Protonated and Non-Protonated Carbon Atoms
13. Asymmetric Self- and Cross-Aldol Reactions of Glycolaldehyde Catalyzed by D-Fructose-6-phosphate Aldolase
14. Ru‐Hbpp‐Based Water‐Oxidation Catalysts Anchored on Conducting Solid Supports
15. Multiple FID Acquisition of Complementary HMBC Data
16. Engineered L-Serine Hydroxymethyltransferase from Streptococcus thermophilus for the Synthesis of α,α-Dialkyl-α-Amino Acids.
17. Regiospecific CH Bond Activation: Reversible H/D Exchange Promoted by CuI Complexes with Triazamacrocyclic Ligands
18. Stepwise Construction of Oligomeric 1,2-Diselenolene Platinum(IV) Complexes
19. Aryl CH Activation by CuII To Form an Organometallic Aryl–CuIII Species: A Novel Twist on Copper Disproportionation
20. Aryl CbH Activation by CuII To Form an Organometallic ArylâCuIII Species: A Novel Twist on Copper Disproportionation This research was supported by MICYT of Spain through project PBQ2000-0548 and with the grant SGR-3102-UG-01 as well as the Distinction award from from CIRIT Generalitat de Catalunya (Spain). An FI doctoral grant from CIRIT to X.R. and financial support from the National Institutes of Health (USA; T.D.P.S. GM-50730; K.O.H. RR-01209) are also acknowledged. SSRL operations are funded by the Department of Energy, Basic Energy Sciences, and the SSRL Structural Molecular Biology Program is supported by the NIH NCRR BTP and the DOE OBER.
21. Cover Picture: Nucleophile Promiscuity of Engineered Class II Pyruvate Aldolase YfaU from <italic>E. Coli</italic> (Angew. Chem. Int. Ed. 14/2018).
22. Aryl CH Activation by CuII To Form an Organometallic Aryl-CuIII Species: A Novel Twist on Copper Disproportionation.
Catalog
Books, media, physical & digital resources
Discovery Service for Jio Institute Digital Library
For full access to our library's resources, please sign in.