
TY  - JOUR
A1  - Jenkins, ID 
A1  - Thang, S 
T1  - Synthesis of some thiosucrose derivatives
JF  - Australian Journal of Chemistry
JO  - Aust. J. Chem.
Y1  - 1984
VL  - 37
IS  - 9
SP  - 1925
EP  - 1930
KW  - 
UR  - https://doi.org/10.1071/CH9841925 
N2  - Treatment of 3,3',4',6'-tetra-O-acetylsucrose in dimethylformamide with thioacetic acid, triphenyl- phosphine and diethyl azodicarboxylate, followed by acetylation, gave 6-thiosucrose octaacetate in good yield. Similar treatment of 4,6:2,1'-di-O-isopropylidenesucrose followed by removal of the isopropylidene groups and acetylation gave 6'-thiosucrose octaacetate. Treatment of sucrose itself under these conditions gave 6,6'-dithiosucrose octaacetate. 6,6'-Dithiosucrose octaacetate was readily converted into 6,6'-dideoxysucrose by treatment with Raney nickel followed by deacetylation. 
ER  -

