Efficient synthesis of substituted tetrahydrothiopyrano[2,3-b]thiopyran-4,5-diones by a double annulation strategy from dialkenoylketene dithioacetals


Autoria(s): Pan W; Dong DW; Ouyang Y; Wu R; Yang Y; Liu Q
Data(s)

2007

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

http://ir.ciac.jl.cn/handle/322003/14319

http://www.irgrid.ac.cn/handle/1471x/150078

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