81086-98-8

Upstream product

• 108-24-7 acetic anhydride 
• 86172-10-3 2,3,4,3',4'-penta-O-acetyl-6,6'-di-O-(tert-butyldiphenylsilyl)sucrose 
• 34382-02-0 2,3,4,3',4'-penta-O-acetylsucrose 
• 57-50-1 Sucrose 
• 81086-92-2 6,6’-di-O-tert-butyldiphenylsilylsucrose 
• 58479-61-1 tert-butylchlorodiphenylsilane 

Downstream Products

• 790685-13-1 1',2,3,3',4,4'-hexa-O-acetyl-6-O-formyl-6'-O-(tert-butyldiphenylsilyl)sucrose 

Relevant academic research and scientific papers

Library of mild and economic protocols for the selective derivatization of sucrose under microwave irradiation

The chemistry of sucrose is very challenging due to its eight hydroxyl groups, three of which are primary, with very similar reactivities, thus control of the chemoselectivity is a central issue. In this work, the selective formation of monounsaturated es

BRANCHED-CHAIN SUCROSES: SYNTHESIS AND WITTIG REACTION OF THE 1'-ALDEHYDO DERIVATIVE OF SUCROSE

The reaction of 2,3,4,3',4'-penta-O-acetylsucrose (1) with 3.3 mol. equv. of tert-butyldiphenylsilyl chloride in pyridine in the presence of 4-dimethylaminopyridine gave the 6,1',6'-tris(tert-butyldiphenylsilyl) derivative 2 (27percent) and the 6,6'-bis(t