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 processFile in questo prodotto:
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