First sequential Mukaiyama-Michael reaction/crossed-Claisen condensation using two molar ketene silyl acetals and one molar α,β-unsaturated esters promoted by a NaOH catalystElectronic supplementary information (ESI) available: Experimental details and NMR spectra. See DOI: 10.1039/c0cc01110j

The NaOH-catalyzed first sequential Mukaiyama-Michael reaction/crossed-Claisen condensation is developed using two molar ketene silyl acetals and one molar α,β-unsaturated esters in either a stepwise or one-pot manner. The NaOH-catalyzed first sequential Mukaiyama-Michael reaction/crossed-Claisen co...

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Hauptverfasser: Tamagaki, Hiroaki, Nawate, Yuuya, Nagase, Ryohei, Tanabe, Yoo
Format: Artikel
Sprache:eng
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Zusammenfassung:The NaOH-catalyzed first sequential Mukaiyama-Michael reaction/crossed-Claisen condensation is developed using two molar ketene silyl acetals and one molar α,β-unsaturated esters in either a stepwise or one-pot manner. The NaOH-catalyzed first sequential Mukaiyama-Michael reaction/crossed-Claisen condensation is developed using two molar ketene silyl acetals and one molar α,β-unsaturated esters in either a stepwise or one-pot manner.
ISSN:1359-7345
1364-548X
DOI:10.1039/c0cc01110j