1996
DOI: 10.1039/p19960000167
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Synthetic studies on 4,5-dihydro-3H-1,2,4-triazole-3,5-diones bearing fluorogenic residues at N-4

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Cited by 31 publications
(31 citation statements)
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“…Mohammad Ali Zolfigol, 1,* Mojtaba Bagherzadeh, 1 Gholamabbas Chehardoli, 1 and Shadpour E. Mallakpour 2 are capable of effecting these oxidations, [18][19][20][21] as far as we know, this transformation is difficult and tricky because these compounds are very sensitive to the oxidizing agents and reaction conditions. However, most of the reported reagents produce by-products that either destroy, or are difficult to remove from, the sensitive triazolinedione.…”
Section: Oxidation Of Urazoles Under Mildmentioning
confidence: 99%
“…Mohammad Ali Zolfigol, 1,* Mojtaba Bagherzadeh, 1 Gholamabbas Chehardoli, 1 and Shadpour E. Mallakpour 2 are capable of effecting these oxidations, [18][19][20][21] as far as we know, this transformation is difficult and tricky because these compounds are very sensitive to the oxidizing agents and reaction conditions. However, most of the reported reagents produce by-products that either destroy, or are difficult to remove from, the sensitive triazolinedione.…”
Section: Oxidation Of Urazoles Under Mildmentioning
confidence: 99%
“…In addition, most of the reported reagents produce byproducts which either destroy the sensitive triazolinediones, or are difficult to remove from the reaction product. Another major drawback of the older procedures is their use of reagents which are either highly toxic or impose serious disposal problems (or both) [9][10][11][12][13].…”
Section: Introductionmentioning
confidence: 99%
“…4 , electrophilic aromatic substitution 5 , dehydrogenating properties 6 and oxidation of alcohols to aldehydes and ketones 7 . All known methods of synthesis of these compounds require oxidation of the corresponding 1,2,4-triazolidine-3,5-diones, more commonly known as urazoles [8][9][10] .…”
Section: Introductionmentioning
confidence: 99%