73488-48-9

Upstream product

• 620630-83-3 1,2:5,6-di-O-cyclohexylidene-α-D-allofuranose 
• 566164-19-0 1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose 

Downstream Products

• 73488-59-2 3,5-di-O-acetyl-6-O-(cyclohex-1-enyl)-1,2-O-cyclohexylidene-α-D-glucofuranose 
• 73488-60-5 3,5-di-O-acetyl-6-O-cyclohexyl-1,2-O-cyclohexylidene-α-D-glucofuranose 

Relevant academic research and scientific papers

The Use of Grignard Reagents in the Synthesis of Carbohydrates. II. The Cleavage of Acetal Protecting Groups in Sugar Derivatives

The selective reaction of acetal protecting groups in sugars with Grignard reagents is described.The treatment of 1,2:5,6-di-O-cyclohexylidene-α-D-glucofuranose (1) with methylmagnesium iodide in benzene-ether at about 85 deg C gave 1,2-O-cyclohexylidene-