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The first example of tetrahydrothieno[3,2-d]azocines synthesis

Дата публикации в реестре: 2020-03-03T14:37:15Z

Аннотация:
Ключевые слова:
3 ethyl 7,8 dimethyl 2 (acetylamino) 6 benzyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 2 (acetylamino) 6 ethyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 2 (acetylamino) 6 methyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 6 benzyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 6 ethyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 6 isopropyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 7,8 dimethyl 6 methyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,7,8 tricarboxylate, 3 ethyl 8 methyl 2 (acetylamino) 6 benzyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 2 (acetylamino) 6 ethyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 2 (acetylamino) 6 isopropyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 2 (acetylamino) 6 methyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 6 benzyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 6 ethyl[(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 6 isopropyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, 3 ethyl 8 methyl 6 methyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3,8 dicarboxylate, azocine derivative, dimethyl 2 [[2 [5 (acetylamino) 4 (ethoxycarbonyl) 2 (methoxymethyl) 3 thienyl]ethyl](methyl)amino]but 2 enedioate, ethyl 6 benzyl 8 [(4 methylphenyl)sulphonyl] 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 6 ethyl 8 [(4 methylphenyl)sulphonyl] 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 6 isopropyl [(4 methylphenyl)sulphonyl] 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 6 methyl 8 [(4 methylphenyl)sulphonyl] 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 2 (acetylamino) 6 benxyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 2 (acetylamino) 6 ethyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 2 (acetylamino) 6 isopropyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 6 benzyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 6 ethyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 6 isopropyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl 6 methyl 2 [(trifluoroacetyl)amino] 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, ethyl 8 acetyl(acetylamino) 6 methyl 4,5,6,9 tetrahydrothieno[3,2 d]azocine 3 carboxylate, tetrahydrothieno[3,2 d]azocine derivative, unclassified drug, article, carbon nuclear magnetic resonance, chemical modification, chemical reaction, chemical structure, crystal structure, one pot synthesis, priority journal, proton nuclear magnetic resonance, X ray crystallography

Тип: Article

Права: open access

Источник: Tetrahedron


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