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1965
1965
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“…The reaction between cyclopentadienones and Nvinyl-2-hydroxyethylamine evolves ethanolamine (9). Trimethylvinylstannane, triethylvinylstannane, and triphenylvinylstannane have been allowed to react at elevated temperatures, i.e., 180-200°, and found to evolve trialkylor triphenylstannane (52,245,246).…”
Section: H-h H-h H-h H-hmentioning
confidence: 99%
“…The reaction between cyclopentadienones and Nvinyl-2-hydroxyethylamine evolves ethanolamine (9). Trimethylvinylstannane, triethylvinylstannane, and triphenylvinylstannane have been allowed to react at elevated temperatures, i.e., 180-200°, and found to evolve trialkylor triphenylstannane (52,245,246).…”
Section: H-h H-h H-h H-hmentioning
confidence: 99%
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