[4+2] Annulation - Convenient Synthesis of Substituted Dihydropyranones in Aqueous Media
| Data(s) |
2009
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|---|---|
| Resumo |
A facile and convenient synthesis of dihydropyranones has been developed by a formal [4+2] annulation of readily available alpha-acetyl ketene S,S-acetals with various aldehydes, involving a tandem aldol reaction and conjugate addition-elimination reaction, in the presence of NaOH in water. |
| Identificador | |
| Idioma(s) |
英语 |
| Fonte |
Ouyang Y;Huang J;Pan W;Liang YJ;Yang Y;Dong DW.[4+2] Annulation - Convenient Synthesis of Substituted Dihydropyranones in Aqueous Media,EUROPEAN JOURNAL OF ORGANIC CHEMISTRY,2009,(12):2003-2009 |
| Palavras-Chave | #DIELS-ALDER REACTION #ACID-CATALYZED CYCLOCONDENSATION #PREPARED CAB CATALYSTS #ONE-STEP SYNTHESIS #ENANTIOSELECTIVE SYNTHESIS #ORGANIC-SYNTHESIS #KETENE DITHIOACETALS #EFFICIENT SYNTHESIS #DANISHEFSKYS DIENE #NATURAL-PRODUCTS |
| Tipo |
期刊论文 |
