Mild thermal reaction of indol-2-yl triphenyl- and methyldiphenyl-phosphorane derived from 2-azido-1-methylindole with enones provides a novel entry to 9-methyl-9H-pyrido[2,3-b]indoles through a tandem aza-Wittig-electrocyclization process

C. Bonini, M. Funicello, P. Spagnolo (2006). Novel Carboline Synthesis using Tandem aza-Wittig-Elecrocyclization Reaction of Indol-2-yl Phosphorane with Enone. SYNLETT, -, 1574-1576.

Novel Carboline Synthesis using Tandem aza-Wittig-Elecrocyclization Reaction of Indol-2-yl Phosphorane with Enone

SPAGNOLO, PIERO
2006

Abstract

Mild thermal reaction of indol-2-yl triphenyl- and methyldiphenyl-phosphorane derived from 2-azido-1-methylindole with enones provides a novel entry to 9-methyl-9H-pyrido[2,3-b]indoles through a tandem aza-Wittig-electrocyclization process
2006
C. Bonini, M. Funicello, P. Spagnolo (2006). Novel Carboline Synthesis using Tandem aza-Wittig-Elecrocyclization Reaction of Indol-2-yl Phosphorane with Enone. SYNLETT, -, 1574-1576.
C. Bonini; M. Funicello; P. Spagnolo
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11585/27811
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