Efficient synthesis of substituted [1,3]thiazolo[3,2-b][1,2,4]triazol-7-ium hexabromotellurates

Fizer, Maksym; Slivka, Mikhailo; Baumer, V. N.

doi:10.1016/j.jorganchem.2021.122044

Search citation statements

Order By: Relevance

Paper Sections

Select...

Table 1 Optimization Of the Reaction Condition...1

Citation Types

Supporting

Mentioning

Contrasting

Year Published

2022

2024

Publication Types

Select...

Article4

Relationship

Self Cite0

Independent4

Authors

Journals

Cited by 4 publications

(1 citation statement)

References 36 publications

Supporting

Mentioning

Contrasting

Order By: Relevance

“…The proposed mechanism in Scheme 4 is in good agreement with the classical conception electrophilic cyclization 18 and is similar to the protonation of isomeric 3-methallylthio-4-phenyl-1,2,4-triazoles by hexabromotelluric acid. 19 The structure of thiazolotriazole 8 was confirmed by complex NMR data and X-ray crystallography. 20…”

Section: Table 1 Optimization Of the Reaction Condition...mentioning

confidence: 89%

An Efficient Catalyst-Free Direct Approach to 5-Polyfluoroalkyl-1,2,4-triazole-3-thiones

et al. 2023

View full text Add to dashboard Cite

An easy to handle high-efficient approach to 5-polyfluoroalkyl-1,2,4-triazole-3-thiones (11 examples, up to 91% yield) is reported. The tautomerism of thione and thiol forms for the obtained products is discussed. A one step procedure for 6,6-dimethyl-3-(trifluoromethyl)-5,6-dihydro[1,3]thiazolo[2,3-c][1,2,4]triazole formation from trifluoroacetic acid and 4-methallylthiosemicarbazide has been developed. The structures of the products were unambiguously determined by complex NMR investigation and by single crystal X-ray diffraction.

show abstract

Section: Table 1 Optimization Of the Reaction Condition...mentioning

confidence: 89%