Results 51 to 60 of about 29,714,115 (240)
Resolution of the racemic amino alcohol derivatives 1−6 is readily achieved to obtain enantiomerically enriched compounds using chiral 1,1‘-bi-2-naphthol and boric acid in solvents such as CH3CN, THF, and MeOH.
Vutukuri Dharma Rao (3027999) +5 more
core +1 more source
Preparation of 5-Bromo-2-naphthol: The Use of a Sulfonic Acid as a Protecting and Activating Group
The preparation of 5-bromo-2-naphthol (4) in three steps from 5-amino-2-naphthol (1) is described. A sulfonic acid group is introduced at the 1-position as an activating and protecting group for the Sandmeyer reaction.
Christopher Abelt +2 more
doaj +1 more source
Novel chromogenic aminopeptidase substrates for the detection and identification of clinically important microorganisms [PDF]
A series of amino acid derivatives 8-10, 42 and 43 have been prepared as chromogenic enzyme substrates in order to detect aminopeptidase activity in clinically important Gram-negative and Gram-positive bacteria.
James, Arthur +6 more
core +1 more source
One‐Pot Synthesis of a Small Synthetic Ligand for Antibody Purification
One‐pot liquid‐phase synthesis of the synthetic ligand B1Al2A2 enables controllable ligand density and efficient capture of IgG and IgY with high recovery and purity, streamlining small‐ligand affinity purification workflows. ABSTRACT The development of synthetic affinity ligands offers a cost‐effective alternative to traditional biological ligands ...
Carolina Mota Natal +8 more
wiley +1 more source
Developmental toxicity of embryonic 1-naphthol exposure in zebrafish
Objective To investigate the toxic effects of embryonic exposure to 1-naphthol (1-NAP) on zebrafish development and explore the possible mechanism. Methods Fertilized zebrafish eggs were exposed to 1-NAP at the concentrations of 40, 80, 160 and 200 μmol ...
REN Pingping +4 more
doaj +1 more source
Nitrooxylation—the installation of nitrate esters (–ONO2) has evolved from classical mixed‐acid protocols to catalytic and mechano‐, flow‐, photo‐, and electrochemical strategies. This review delineates ionic and radical manifolds for C–ONO2 bond formation, emphasizing mechanistic control, selected substrate scope, and selectivity.
Jayanta Dey, Dmitry Katayev
wiley +1 more source
Treatment of BINOL with a boron subphthalocyanine derivative resulted in the formation of a complex coordinated to an oxa[4]helicene derivative, which is generated via a ring‐closure reaction of BINOL. In contrast, treatment of the monomethyl ether of 1,1′‐bi‐2‐naphthol (BINOL) afforded the expected axially coordinated complex.
Shafikul Islam +5 more
wiley +1 more source
Accurate intermolecular binding energies of 1-naphthol to benzene and cyclohexane
Accurate dissociation energies were determined for gas-phase complexes between 1-naphthol and benzene, d6-benzene and cyclohexane, using the stimulated emission pumping resonant two-photon ionization spectroscopy technique in supersonic jets.
Buergi, Thomas +3 more
core +1 more source
Several new chiral cyclic hypervalent iodine(III) reagents have been synthesized and characterized. Carbon‐based ligands were successfully installed onto the hypervalent iodine centers, giving thus access to novel chiral cyano‐, trifluoromethyl‐ or alkynyl‐bearing λ3‐iodanes.
Emmanuel Valzer +4 more
wiley +1 more source
Efficient Cleavage of pUC19 DNA by Tetraaminonaphthols
In an attempt to create models of phosphodiesterases, we previously investigated bis(guanidinium) naphthols. Such metal‐free anion receptors cleaved aryl phosphates and also plasmid DNA.
Catharina Kost +3 more
doaj +1 more source

