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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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. |
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ISSN: | 1359-7345 1364-548X |
DOI: | 10.1039/c0cc01110j |