Results 31 to 40 of about 4,839 (215)

Access to highly substituted oxazoles by the reaction of α-azidochalcone with potassium thiocyanate

open access: yesBeilstein Journal of Organic Chemistry, 2020
The reactivity of α-azidochalcones has been explored for the preparation of highly substituted oxazoles via a 2H-azirine intermediate. The azidochalcones, when treated with potassium thiocyanate in the presence of potassium persulfate, lead to 2,4,5 ...
Mysore Bhyrappa Harisha   +4 more
doaj   +1 more source

Enantiomeric Separation of New Chiral Azole Compounds

open access: yesMolecules, 2021
Twelve new azole compounds were synthesized through an ene reaction involving methylidene heterocycles and phenylmaleimide, producing four oxazoles, five thiazoles, and one pyridine derivative, and ethyl glyoxylate for an oxazole and a thiazole compound.
Marziyeh E. Kenari   +9 more
doaj   +1 more source

Monosubstituted Oxazoles. 1. Synthesis of 5-Substituted Oxazoles by Directed Alkylation

open access: yes, 2016
A general method is presented for synthesis of 2-(methylthio)-5-substituted oxazoles 2. Deprotonation of the readily available 2-(methylthio)oxazole (1) with n-BuLi occurs smoothly in the presence of TMEDA and regiospecifically at C5.
Tadeusz F. Molinski (1313355)   +1 more
core   +2 more sources

Synthesis of 1,3-Oxazoles via Van Leusen Reaction in a Pressure Reactor and Preliminary Studies of Cations Recognition

open access: yesProceedings, 2019
Six 1,3-oxazoles were synthetized in moderate to good yields by Van Leusen reaction in a pressure reactor. The methodology allowed to decrease the reaction times reported in the literature from hours to 20 min.
Verónica G. García-Ramírez   +4 more
doaj   +1 more source

Pyridine C─N Transposition via Cycloaddition–Cycloreversion

open access: yesAngewandte Chemie, EarlyView.
Transposition of pyridine nitrogen from the 4‐ to the 3‐position is described using two open and shut sequences: a nucleophile addition ring‐open ring‐closure, followed by a nitrile Diels–Alder cycloaddition cycloreversion. The nitrogen swap is particularly effective for tertiary alkyl substituents, transforming easily accessible para‐alkylated ...
Aífe Conboy, Michael F. Greaney
wiley   +2 more sources

Diazocarbonyl and Related Compounds in the Synthesis of Azoles

open access: yesMolecules, 2021
Diazocarbonyl compounds have found numerous applications in many areas of chemistry. Among the most developed fields of diazo chemistry is the preparation of azoles from diazo compounds.
Anton Budeev   +3 more
doaj   +1 more source

Gold Catalyzed Multicomponent Reactions beyond A3 Coupling

open access: yesMolecules, 2018
The preparation of complex architectures has inspired the search for new methods and new processes in organic synthesis. Multicomponent reactions have become an interesting approach to achieve such molecular diversity and complexity.
Renso Visbal   +3 more
doaj   +1 more source

A new synthesis of oxazoles

open access: yes, 1980
Oxazoles are prepared from the ketoximes in a single pot ...
Bhatt, MV, Reddy, Gaddam Subba
core   +2 more sources

Simple and Expedient Access to Novel Fluorinated Thiazolo- and Oxazolo[3,2-a]pyrimidin-7-one Derivatives and Their Functionalization via Palladium-Catalyzed Reactions

open access: yesMolecules, 2022
An efficient, versatile, and one-pot method for the preparation of novel fluorinated thiazolo- and oxazolo[3,2-a]pyrimidin-7-ones is described from 2-aminothiazoles or 2-amino-oxazoles and fluorinated alkynoates.
Wafa Blancou   +4 more
doaj   +1 more source

1,4- Addition of diazomethane to a heterodiene: a direct preparation of the oxazolic ring

open access: yesAnais da Academia Brasileira de Ciências, 2007
The reaction of naphthoquinone-oximes (3) and (4) with diazomethane yields directly, in one step, the oxazoles (5) and (6), respectively.A reação das naphthoquinona-oximas (3) e (4) com diazometano fornece diretamente, em uma etapa, os oxazóis (5) e (6),
Flávio da S. Emery   +9 more
doaj   +1 more source

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