144946-76-9

Upstream product

• 100-39-0 benzyl bromide 
• 27894-78-6 1β-(p-chlorophenylthio)maltose 

Downstream Products

• 108811-21-8 2,3,6-tri-O-benzyl-4-O-(2′,3′,4′,6′-tetra-O-benzyl-α-D-glucopyranosyl)-D-glucopyranoside 
• 139172-73-9 2,2',3,3',4',6,6'-hepta-O-benzyl-N-(<1'',2''-bis(methoxycarbonyl)vinyl>oxy)-D-maltonimido-1,4-lactone 
• 144946-82-7 2,2',3,3',4',6,6'-hepta-O-benzyl-N-hydroxy-D-maltonimido-1,4-lactone 
• 144946-83-8 2,3,6-tri-O-benzyl-4-O-(2,3,4,6-tetra-O-benzyl-α-D-glucopyranosyl)-D-glucose oxime 

Relevant academic research and scientific papers

Thermal Rearrangement of Alkyl O-Vinylcarbohydroximates to 2-Alkyloxazoles

Alkyl O-vinylcarbohydroximates, lactoxime O-vinyl ethers, and sugar lactoxime O-vinyl ethers undergo a novel thermal rearrangement to afford the corresponding 2-alkyloxazoles, 2-(ω-hydroxyalkyl)oxazoles, and oxazoles bearing a sugar moiety, respectively.This rearrangement can also occur under photochemical conditions.