Results 11 to 20 of about 3,487 (237)

γ-aminobutyric acid and collagen peptides as recyclable bifunctional biocatalysts for the solvent-free one-pot synthesis of 2-aminobenzothiazolomethyl-2-naphthols

open access: yesGreen Chemistry Letters and Reviews, 2018
γ-aminobutyric acid (GABA) and Isinglass a collagen peptide have been utilized as highly efficient bifunctional biocatalysts for the efficient and convenient synthesis of 2-aminobenzothiazolomethyl-2-naphthols through a one-pot three-component Mannich ...
Maryam Fardpour   +2 more
doaj   +2 more sources

The effect of 4-substitution on some properties of the O–H bond in 1-naphthols [PDF]

open access: yes, 1974
The effects of 4-substitution on some of those properties of the O–H bond in 1-naphthols which reflect its hydrogen bonding tendency have been studied.
Bernard J. Hawley (7166798)
core   +7 more sources

Autoxidation of 2-Naphthols [PDF]

open access: yes, 1974
This thesis describes an investigation of the structural factors which influence the susceptibility of substituted 2-naphthols to autoxidation. The mechanism of these processes is discussed in detail in the light of the results obtained. Previous workers
Brady, Paul Anthony
core   +6 more sources

Rhodium(III)-Catalyzed [4+2] Annulation via C-H Activation: Synthesis of Multi-Substituted Naphthalenone Sulfoxonium Ylides

open access: yesMolecules, 2019
A convenient Rh(III)-catalyzed C-H activation and cascade [4+2] annulation for the synthesis of naphthalenone sulfoxonium ylides has been developed. This method features perfect regioselectivity, mild and redox-neutral reaction conditions, and broad ...
Xiaohan Song   +4 more
doaj   +1 more source

Metal-free oxidative cross-coupling enabled practical synthesis of atropisomeric QUINOL and its derivatives

open access: yesNature Communications, 2021
1-(Isoquinolin-1-yl)naphthalen-2-ol (QUINOL) is an atropisomeric heterobiaryl that serves as a platform for the synthesis of other biaryl ligands useful in asymmetric catalysis. Here, the authors report a straightforward oxidative cross-coupling reaction
Peng-Ying Jiang   +4 more
doaj   +1 more source

Salicylic Acid-catalyzed Three-component Synthesis of 1-Amido/thioamidoalkyl-2-naphthols Under Solvent-free Conditions

open access: yesOrbital: The Electronic Journal of Chemistry, 2019
A simple, efficient, and green procedure for the solvent-free synthesis of 1-amido/thioamidoalkyl-2-naphthols by one-pot stirring of starting reactants at 100 °C has been introduced.
Hassan Darbandi, Hamzeh Kiyani
doaj   +3 more sources

THE BETA-NAPHTHOL VS. HYDRO-NAPHTHOL CONTENTION. [PDF]

open access: yesJAMA: The Journal of the American Medical Association, 1889
"Who shall decide when doctors disagree?" says the poet, with as close accordance with a general truth as reason and poetry require. Yet we shall always find, even in the case of the disagreement of doctors, criteria by which rational decision may be reached. In the first place, the opinions of individual doctors, as well as of persons not doctors, are
openaire   +1 more source

Carboxylation of hydroxyarens with metal alkyl carbonates

open access: yesGreen Processing and Synthesis, 2015
The objective of this work was to investigate the possibility of using alkali metal salts of ethylcarbonic acid as a carboxylating reagent in phenol (naphthols) carboxylation and developing a new and simple method for the synthesis of hydroxybenzoic and ...
Suerbaev Khakim A.   +2 more
doaj   +1 more source

Selenium-Mediated Synthesis of Tetrasubstituted Naphthalenes through Rearrangement

open access: yesMolecules, 2015
New β-keto ester substituted stilbene derivatives have been synthesized and cyclized with selenium electrophiles in the presence of Lewis acids. This now allows access to 1,2,3,4-tetrasubstituted naphthalene derivatives as cyclization and rearrangement ...
James Tancock, Thomas Wirth
doaj   +1 more source

Enhancement of Dissymmetry Factors Through Axial Elongation of Hetero[n]helicenes

open access: yesAngewandte Chemie, EarlyView.
A benzofuran scaffolding strategy enables the synthesis of hetero[9]‐, [12]‐, and [15]helicenes. Structural and chiroptical analyses demonstrate that systematic axial elongation increases helical distortion and significantly amplifies luminescence dissymmetry.
Jeppe S. Mogensen   +7 more
wiley   +2 more sources

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