The chemistry of alpha-oxo ketene cyclic dithioacetal .36. Studies on silica G catalyzed decomposition of adducts of beta,beta-1,3-propylenedithio-alpha,beta-unsaturated arylketones with grignard reagents


Autoria(s): Dong DW; Xie ZL; Liu Q; Yang ZY; Liu JF
Data(s)

1997

Resumo

beta, beta-1, 3-Piopylenedithio-alpha, beta-unsaturated arylketones 2 via chemoselective 1,2-addition with allyl or benzyl Grignard reagents afforded the corresponding carbinols 3 and 4. Catalysed by silica gel, the carbinols 3 and 4 were converted to the beta,gamma-unsaturated arylketones 5, 6. The mechanism and reaction condition were discussed.

Identificador

http://ir.ciac.jl.cn/handle/322003/24439

http://www.irgrid.ac.cn/handle/1471x/156947

Idioma(s)

中文

Fonte

Dong DW;Xie ZL;Liu Q;Yang ZY;Liu JF.The chemistry of alpha-oxo ketene cyclic dithioacetal .36. Studies on silica G catalyzed decomposition of adducts of beta,beta-1,3-propylenedithio-alpha,beta-unsaturated arylketones with grignard reagents,CHEMICAL JOURNAL OF CHINESE UNIVERSITIES-CHINESE,1997,18(1):68-72

Palavras-Chave #CYCLOAROMATIZATION
Tipo

期刊论文