Preparation of new trifluoromethyl substituted tri- and tetracyclic heterocycles with Peganin skeleton from a methyl 3,3,3-trifluoropyruvate 2-aminobenzylamine adduct
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作者:
Dolensky, B
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机构:INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Dolensky, B
Kvicala, J
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机构:INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Kvicala, J
Paleta, O
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机构:INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Paleta, O
Cejka, J
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机构:INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Cejka, J
Ondracek, J
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机构:INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Ondracek, J
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[1] INST CHEM TECHNOL,DEPT ORGAN CHEM,PRAGUE 16628 6,CZECH REPUBLIC
[2] INST CHEM TECHNOL,DEPT SOLID STATE CHEM,PRAGUE 16628 6,CZECH REPUBLIC
Addition of 2-aminobenzylamine to methyl trifluoropyruvate afforded methyl 2-((2-aminobenzyl)amino) -3.3,3-trifluoro-2-hydroxypropionate, which reacted with various ketones to give new fluorinated tricyclic and tetracyclic heterocycles with the skeleton of the alkaloid Peganin. Copyright (C) 1996 Elsevier Science Ltd