Efficient synthesis of substituted tetrahydrothiopyrano[2,3-b]thiopyran-4,5-diones by a double annulation strategy from dialkenoylketene dithioacetals
Data(s) |
2007
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Resumo |
An efficient synthetic procedure for substituted 2,3,6,7tetrahydrothiopyrano [2,3-b] thiopyran-4,5 -diones by a double annulation strategy is described. The ring systems are made in good yields from readily available dialkenoylketene dithioacetals in the presence of either sodium sulfide nonahydrate/N,N-dimethylformamide (DMF) or a sodium hydride/DMF/amine system. |
Identificador | |
Idioma(s) |
英语 |
Fonte |
Pan W;Dong DW;Ouyang Y;Wu R;Yang Y;Liu Q.Efficient synthesis of substituted tetrahydrothiopyrano[2,3-b]thiopyran-4,5-diones by a double annulation strategy from dialkenoylketene dithioacetals,SYNTHESIS-STUTTGART,2007 ,(14):2115-2120 |
Palavras-Chave | #DIELS-ALDER REACTIONS #RAMBERG-BACKLUND #ORGANIC-SYNTHESIS #FACILE #ANION #THIOACETALIZATION #THIATHROMBOXANES #CYCLOPENTENONES #2H-THIOPYRANS #REARRANGEMENT |
Tipo |
期刊论文 |