Racemic and enantiopure benzofuranmethanamines 5a–c have been reacted with N-Boc-3-(4-cyanophenyl)oxaziridine to give N-Boc-hydrazines 7a–c, which have in turn been transformed by deprotection and cyclisation into triazoles 4a–c, potent antiaromatase agents, in good overall yield and with high enantiomeric excess.

Messina, F., Botta, M., Corelli, F., Paladino, A. (2000). Synthesis of Enantiomerically Pure 1[(-(benzofuran-2-yl)arylmethyl]-1H-1,2,4-triazoles, Antifungal and Antiaromatase Agents. TETRAHEDRON, 11(24), 4895-4901 [10.1016/S0957-4166(00)00486-9].

Synthesis of Enantiomerically Pure 1[(-(benzofuran-2-yl)arylmethyl]-1H-1,2,4-triazoles, Antifungal and Antiaromatase Agents

BOTTA, M.;
2000-01-01

Abstract

Racemic and enantiopure benzofuranmethanamines 5a–c have been reacted with N-Boc-3-(4-cyanophenyl)oxaziridine to give N-Boc-hydrazines 7a–c, which have in turn been transformed by deprotection and cyclisation into triazoles 4a–c, potent antiaromatase agents, in good overall yield and with high enantiomeric excess.
2000
Messina, F., Botta, M., Corelli, F., Paladino, A. (2000). Synthesis of Enantiomerically Pure 1[(-(benzofuran-2-yl)arylmethyl]-1H-1,2,4-triazoles, Antifungal and Antiaromatase Agents. TETRAHEDRON, 11(24), 4895-4901 [10.1016/S0957-4166(00)00486-9].
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11365/2706
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