share
Chin. J. Org. Chem. ›› 2005, Vol. 25 ›› Issue (07): 819-821. Previous Articles Next Articles
Original Articles
林春2,于海丰1,2,刘群*,1,侯冬岩2
收稿日期:
修回日期:
发布日期:
通讯作者:
LIN Chun2,YU Hai-Feng1,2,LIU Qun*,1,HOU Dong-Yan2
Received:
Revised:
Published:
Contact:
Share
3-(1,3-Dithian-2-ylidene)-pentane-2,4-dione (1a) and 2-[2-chloro-1-(1-chlorovinyl)-allylidene]- 1,3-dithiane (1b), prepared readily and used conveniently as odorless and efficient 1,3-propanedithiol equivalent, were studied in thioacetalization reaction.
Key words: 3-(1,3-dithian-2-ylidene)-pentane-2,4-dione, 1,3-propanedithiol equivalent, thio-acetalization, 1,3-dithiane, 2-[2-chloro-1-(1-chlorovinyl)-allylidene]-1,3-di- thiane
LIN Chun2,YU Hai-Feng1,2,LIU Qun*,1,HOU Dong-Yan2. Thioacetalization Reaction of Odorless α-OxoketeneDithioacetals as 1,3-Propanedithiol Equiva-lent[J]. Chin. J. Org. Chem., 2005, 25(07): 819-821.
Export EndNote|Reference Manager|ProCite|BibTeX|RefWorks