Publication | Closed Access
Synthesis of 1,2,4‐Triazolo[4,3‐d][1,2,4]Triazepines By 1,3‐Dipolar Cycloaddition
17
Citations
10
References
1992
Year
Medicinal ChemistryDiversity Oriented SynthesisHeterocyclicPreferred OrientationNatural SciencesDiversity-oriented SynthesisAm 1Organic Chemistry1,3‐Dipolar CycloadditionStereoselective SynthesisChemistryHeterocycle ChemistryPharmacology
Abstract The reaction of N‐aryl‐C‐ethoxycarbonyl nitrilimines with [1,2,4]triazepin‐3,5‐dithione leads to title compounds. The 1,3‐dipolar cycloaddition is completely peri and regioselective. The preferred orientation of addition is predicted correctly by AM 1 calculation.
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