Results 191 to 200 of about 10,973 (280)
Modeling Mo(VI)═O Biologically Related Interactions with Oximes and Hydroxylamines: Implications for Uranium Seawater Extraction. [PDF]
Passadis SS +10 more
europepmc +1 more source
Rhodium‐Catalyzed Regioselective Addition of N‐Hydroxyl Imides to Internal Alkynes
An intermolecular rhodium‐catalyzed regioselective addition of N‐hydroxyl imides to internal alkynes leads to branched O‐allyl compounds, which can be readily transformed to allylic alcohols and O‐allyl hydroxylamines after deprotection. Isotopic labelling experiments suggest a plausible reaction mechanism.
Zi Liu, Bernhard Breit
wiley +1 more source
Skeletal Editing Strategies Driven by Total Synthesis. [PDF]
Kim SF +3 more
europepmc +1 more source
Synthesis of Hydroxylamine Derivatives. I : Mannich Reaction with Substituted Hydroxylamine
T, Irikura, K, Kasuga
openaire +3 more sources
Abstract BACKGROUND This study assessed the effects of dietary carnosine during the in vitro digestion of a healthy meal model based on the Mediterranean diet, comprising lean pork enriched with two levels of carnosine, whole grain bread, tomato, onion, and olive oil.
Yi Yao Li +6 more
wiley +1 more source
Decoupling Electron and Proton Transfer in Noncontact Catalytic Hydrogenation of Nitroaromatics. [PDF]
Liang Z, Wu Q, Yang Z, Zheng N.
europepmc +1 more source
Metal‐Free, Chemoselective Reduction of Aromatic Nitro Compounds in Water at Room Temperature
A metal‐free, rapid, and chemoselective nitro reduction of aromatic compounds is developed using tetrahydroxydiboron as reducing agent and 4,4′‐bipyridine as organocatalyst. This green method provides an efficient entry to aromatic amines with high functional group tolerance in excellent yields under mild conditions using water as solvent. A metal‐free,
Maria Batzaki +2 more
wiley +1 more source
Three-Component Catalytic Amino Etherification of Alkenes: Enabled by Silyl Ether-Promoted C-O Coupling. [PDF]
Feng G, Nguyen AL, Wang Q.
europepmc +1 more source
Flavodiiron proteins (FDPs) are di‐iron enzymes that reduce NO and/or O2 with distinct substrate selectivity. We have produced E. coli FDP variants targeting second coordination‐sphere residues and determined their structures. Although the kinetics remained unchanged, the E.
Patrícia T. Borges +8 more
wiley +1 more source
A reactivity programmed cascade between carbyne equivalents and allylic benzoates was developed that sequentially orchestrates all three reactivity modes of carbyne equivalents, enabling the rapid installation of three σ‐bonds at a single carbon center and providing efficient, scalable access to structurally diverse spirocyclic ethers. ABSTRACT Carbyne
Jianke Su +5 more
wiley +2 more sources

