Results 1 to 10 of about 40,394 (295)

Multicomponent syntheses of pyrazoles via (3 + 2)-cyclocondensation and (3 + 2)-cycloaddition key steps [PDF]

open access: yesBeilstein Journal of Organic Chemistry
Pyrazoles are rarely found in nature but are traditionally used in the agrochemical and pharmaceutical industries, while other areas of use are also actively developing. However, they have also found numerous other applications.
Ignaz Betcke   +3 more
doaj   +2 more sources

Regio- and Stereoselective Switchable Synthesis of (E)- and (Z)-N-Carbonylvinylated Pyrazoles

open access: yesMolecules, 2023
Regio- and stereoselective switchable synthesis of (E)- and (Z)-N-carbonylvinylated pyrazoles is first developed by using the Michael addition reaction of pyrazoles and conjugated carbonyl alkynes.
Xue Zhang   +3 more
doaj   +1 more source

Substituted Pyrazoles and Their Heteroannulated Analogs—Recent Syntheses and Biological Activities

open access: yesMolecules, 2021
Pyrazoles are considered privileged scaffolds in medicinal chemistry. Previous reviews have discussed the importance of pyrazoles and their biological activities; however, few have dealt with the chemistry and the biology of heteroannulated derivatives ...
Mohamed Ramadan   +4 more
doaj   +1 more source

Acid Catalyzed N-Alkylation of Pyrazoles with Trichloroacetimidates

open access: yesOrganics, 2022
N-Alkyl pyrazoles are important heterocycles in organic and medicinal chemistry, demonstrating a wide range of biological activity. A new method for the N-alkylation of pyrazoles has been developed using trichloroacetimidate electrophiles and a Brønsted ...
Rowan I. L. Meador   +2 more
doaj   +1 more source

Natural and Biomimetic Antitumor Pyrazoles, A Perspective

open access: yesMolecules, 2020
The present review presents an overview of antitumor pyrazoles of natural or bioinspired origins. Pyrazole compounds are relatively rare in nature, the first ones having been reported in 1966 and being essentially used as somniferous drugs.
Nádia E. Santos   +3 more
doaj   +1 more source

SUBSTITUTED 4-NITROSOPYRAZOLES IN THE DIELS-ALDER REACTION

open access: yesSiberian Journal of Life Sciences and Agriculture, 2021
Background. 4-Nitrosopyrazoles have become widespread in the pharmaceutical industry and in chemistry due to their high reactivity and biological activity. However, the interaction of 3,5-substituted 4-nitroso-1H-pyrazoles with diene hydrocarbons has not
Darya S. Volkova   +4 more
doaj   +1 more source

Synthesis and Characterization of 3-Methyl-1-(4-(trifluoromethyl)phenyl)indeno [1,2-c]pyrazol-4(1H)-one

open access: yesMolbank, 2022
Pyrazoles have potential applications in the agrochemical and medicinal chemistry industries as pesticides, anti-inflammatory medications, and antitumor drugs. Fluorinated fused-ring pyrazoles may also possess medicinally useful properties.
Linh Lam, Sang H. Park, Joseph Sloop
doaj   +1 more source

Carbamidine-substituted Pyrazoles [PDF]

open access: yesNature, 1951
THE ease with which 1-substituted pyrazoles may be converted into the free imino compounds varies with the nature of the 1-substituent and the reacting substance. Thus, 1,3,5-trimethyl pyrazole may be nitrated1 and 1-phenyl pyrazole reduced to the pyrazoline2 without loss of the N-methyl or N-phenyl groups respectively.
F L, SCOTT, C M B, MURPHY, J, REILLY
openaire   +2 more sources

Nickel-Catalyzed, One-Pot Synthesis of Pyrazoles

open access: yesChemistry Proceedings, 2022
Recently, multi-component, one-pot reactions have been shown to be efficient and environmentally friendly methods compared to traditional, linear-step syntheses.
Nassima Medjahed   +4 more
doaj   +1 more source

Preparation of novel acyl pyrazoles and triazoles by means of oxidative functionalization reactions

open access: yesHeterocyclic Communications, 2023
Novel acyl pyrazoles and acyl triazoles have been prepared by means of the oxidative amidation of aldehydes in the presence of the requisite azole. Yields range from modest to good in both cases, and some limitations of the substrate scope have been ...
Wadey Geoffrey P.   +3 more
doaj   +1 more source

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