Thermal Rearrangement of Allyl Substituted Unsymmetric 4H-1,2,4-Triazoles to the Corresponding 1H-1,2,4-triazoles
نویسندگان
چکیده
منابع مشابه
Regioselectivity in the Thermal Rearrangement of Unsymmetrical 4-Methyl-4H-1,2,4-triazoles to 1-Methyl-1H- 1,2,4-triazoles
The rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles. This lends support to a proposed mechanism for the rearrangement that involves consecutive nucleophilic displacements steps.
متن کاملOrganocatalytic routes toward substituted 1,2,3-triazoles.
The present feature article describes the different organocatalytic routes for the synthesis of substituted 1,2,3-triazoles. This methodology has recently gained much attention due to its many advantages like high regioselectivity, substrate scope, high yields, and access to novel molecules. The review is divided into 4 different sections based on the active intermediate of the triazole synthes...
متن کاملBleaching activity of 4-phenyl-3-(substituted benzylthio)-4H-1,2,4-triazoles.
A variety of 4-aryl- and 4-alkyl-3-(substituted benzylthio)-4H-1,2,4-triazoles were prepared and evaluated for their bleaching activity by the lettuce seedling test. Among the series of tested compounds, 4-(3-fluorophenyl)-3-(4-trifluoromethylbenzylthio)-4H-1,2,4-triazole (39) exhibited the highest bleaching activity, causing complete bleaching symptoms at 10 microM. In the dark condition, comp...
متن کاملSynthesis and base-pairing properties of C-nucleotides having 1-substituted 1H-1,2,3-triazoles.
Oligonucleotides including C-nucleotides having 1-substitued 1H-1,2,3-triazoles as artificial nucleobases were conveniently synthesized by the post-elongation modification method using the copper(I)-catalyzed alkyne-azide 1,3-dipolar cycloaddition (CuAAC) reaction. The base-pairing properties of the triazole nucleobase analogs in forming duplexes with oligonucleotides were investigated by the T...
متن کاملDFT studies on tautomerism of C5-substituted 1,2,3-triazoles
DFT (B3PW91/6-311þþG**), ab initio (HF/6-311þþG**), and single point CCSD(T)/6-311þþG**//B3PW91/6311þþG** calculations were performed to investigate the stability and tautomerism of the C5-substituted 1,2,3-triazoles. Three different tautomers are possible for the substituted 1,2,3-triazoles: N1–H, N2–H, and N3–H. For all the substituents applied, the most stable is the N2–H tautomer. Out of th...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
ژورنال
عنوان ژورنال: Molecules
سال: 2001
ISSN: 1420-3049
DOI: 10.3390/60500481