Methyl benzothiazol-2-yliminotrifluoropyruvates in the Diels-Alder aza-reaction with cyclopentadiene and cyanoamines
摘要:
Methyl trifluoropyruvate benzothiazol-2-ylimines exhibit both a heterodiene and a dienophile properties in the Diels-Alder aza-reaction with cyclopentadiene and cyanoamines, leading to the formation of 4-substituted 2-trifluoromethyl-2H-[1,3,5]triazine[2,1-b][1,3]benzothiazole and 2-benzothiazol-2-yl-3-trifluoromethyl-2-azabicyclo[2.2.1]hept-5-ene, respectively.
Methyl benzothiazol-2-yliminotrifluoropyruvates in the Diels-Alder aza-reaction with cyclopentadiene and cyanoamines
摘要:
Methyl trifluoropyruvate benzothiazol-2-ylimines exhibit both a heterodiene and a dienophile properties in the Diels-Alder aza-reaction with cyclopentadiene and cyanoamines, leading to the formation of 4-substituted 2-trifluoromethyl-2H-[1,3,5]triazine[2,1-b][1,3]benzothiazole and 2-benzothiazol-2-yl-3-trifluoromethyl-2-azabicyclo[2.2.1]hept-5-ene, respectively.