Results 231 to 240 of about 16,084 (302)
Solid Phase Synthesis, DFT Calculations, Molecular Docking, and Biological Studies of Symmetrical N 2,N 4,N 6-Trisubstituted-1,3,5-triazines. [PDF]
Akbar W +10 more
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A theoretical study on the corrosion inhibition of Cu surfaces using 4-amino-3-thioxo-6-methyl-1,2,4-triazine-5-one and its derivatives. [PDF]
Jafarzadegan Z +3 more
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Rearrangement Cascade Initiated by Nucleophilic Benzyne Attack on 3,6-Di(2-pyridyl)-1,2-diazines. [PDF]
Schöntag J +5 more
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Cysteine-Specific Multifaceted Bioconjugation of Peptides and Proteins Using 5-Substituted 1,2,3-Triazines. [PDF]
Zuo Q +12 more
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Chromatographic Reviews, 1970
Abstract The major areas of diverse paper, thin-layer, gas and column chromatographic analyses have been reviewed with special emphasis on procedures used for the elaboration of compound homogeneity, metabolism, degradation and mode of action of a variety of 1,3,5-triazines that are of pesticidal, pharmaceutical, chemosterilant and industrial ...
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Abstract The major areas of diverse paper, thin-layer, gas and column chromatographic analyses have been reviewed with special emphasis on procedures used for the elaboration of compound homogeneity, metabolism, degradation and mode of action of a variety of 1,3,5-triazines that are of pesticidal, pharmaceutical, chemosterilant and industrial ...
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Dalton Trans., 2004
The synthesis of TAS+ C3N3F4- (1) (TAS+ = (Me2N)3S+) and the reactions of 1 with Me3SiOSiMe3 and Me3SiCF3 to give TAS+ C3N3F2O- (2) and TAS+[(NCF)(NCCF3)(NC(CF3)(2)]- (4) are reported. An isomer of 4, TAS+[(NCCF3)2(NCFCF3)]-, compound 6, was obtained by fluoride ion addition to (CF3CN)3.
Melanie, Kingston +3 more
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The synthesis of TAS+ C3N3F4- (1) (TAS+ = (Me2N)3S+) and the reactions of 1 with Me3SiOSiMe3 and Me3SiCF3 to give TAS+ C3N3F2O- (2) and TAS+[(NCF)(NCCF3)(NC(CF3)(2)]- (4) are reported. An isomer of 4, TAS+[(NCCF3)2(NCFCF3)]-, compound 6, was obtained by fluoride ion addition to (CF3CN)3.
Melanie, Kingston +3 more
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2005
Abstract Despite the widespread use of these chemicals, relatively little is known regarding their potential effects on the health of wildlife and humans. In light of such widespread use and limited information about health effects, there has been an in creasing interest in potential detrimental impacts due to unintended exposure ...
Timothy S Gross, R Heath Rauschenberger
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Abstract Despite the widespread use of these chemicals, relatively little is known regarding their potential effects on the health of wildlife and humans. In light of such widespread use and limited information about health effects, there has been an in creasing interest in potential detrimental impacts due to unintended exposure ...
Timothy S Gross, R Heath Rauschenberger
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Journal of Heterocyclic Chemistry, 1987
AbstractA convenient route is reported for the synthesis of substituted 1,3,4‐thiadiazolo[3,2‐a]‐1,3,5‐triazine‐5,7‐diones and isoxazolo[2,3‐a]‐1,3,5‐triazines. Condensation of the appropriately substituted 2‐amino‐1,3,4‐thiadiazole and 3‐aminoisoxazole with phenoxycarbonyl isocyanate provides the desired target compounds in fair yield.
Mohamed M. El‐Kerdawy +3 more
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AbstractA convenient route is reported for the synthesis of substituted 1,3,4‐thiadiazolo[3,2‐a]‐1,3,5‐triazine‐5,7‐diones and isoxazolo[2,3‐a]‐1,3,5‐triazines. Condensation of the appropriately substituted 2‐amino‐1,3,4‐thiadiazole and 3‐aminoisoxazole with phenoxycarbonyl isocyanate provides the desired target compounds in fair yield.
Mohamed M. El‐Kerdawy +3 more
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Journal of Macromolecular Science: Part A - Chemistry, 1971
Abstract High molecular weight soluble polyphenyl-as-triazines were prepared at ambient temperature in m-cresol by the cyclopolycondensation of 2,6-pyridinediyl dihydrazidine (diamidrazone) with various aromatic dibenzil type reactants. Clear lemon yellow films, which exhibited good toughness and flexibility, were cast from solution.
P. M. Hergenrother, D. E. Kiyohara
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Abstract High molecular weight soluble polyphenyl-as-triazines were prepared at ambient temperature in m-cresol by the cyclopolycondensation of 2,6-pyridinediyl dihydrazidine (diamidrazone) with various aromatic dibenzil type reactants. Clear lemon yellow films, which exhibited good toughness and flexibility, were cast from solution.
P. M. Hergenrother, D. E. Kiyohara
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