126569-19-5

Upstream product

• 98-88-4 benzoyl chloride 
• 121614-22-0 3-Amino-3-((S)-2,2-dimethyl-[1,3]dioxolan-4-yl)-propionic acid methyl ester 
• 121614-04-8 (1S)-N-<<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>methylene>-1-phenylethylamine N-oxide 
• 121614-22-0 methyl (3R,4'S)-3-(2',2'-dimethyl-1',3'-dioxolan-4'-yl)-3-aminopropanoate 
• 15186-48-8 2,3-isopropylidene-glyceraldehyde 
• 121614-10-6 methyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate 
• 121614-10-6 methyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate 
• 121614-18-4 methyl (4S)-3--4,5-(isopropylidenedioxy)pentanoate 
• 121614-05-9 N-<<(4S)-2,2-dimethyl-1,3-dioxolan-4-yl>methylene>benzhydrylamine N-oxide 
• 91190-38-4 N-benzyl-2,3-O-isopropylidene-D-glyceraldehyde nitrone 
• 121614-06-0 Methyl (3R,4S)-3--4,5-(isopropylidenedioxy)-pentanoate 

Downstream Products

• 121701-20-0 (3S,4S)-5-acetoxy-3-benzoylamino-4-pentanolide 
• 121701-19-7 (3R,4S)-5-acetoxy-3-benzoylamino-4-pentanolide 
• 126569-20-8 3-benzoylamino-2,3-dideoxy-D-ribo-pentapyranose 

Relevant academic research and scientific papers

Chemistry of O-Silylated Ketene Acetals: Stereocontrolled Synthesis of 3-Benzoylamino-2,3-dideoxypentoses by a 1,3-Addition to Chiral Nitrones

The stereochemistry of 1,3-addition of ketene acetals (1a,b) to the chiral nitrones (4a-d) derived from 2,3-O-isopropylidene-D-glyceraldehyde was examined.The reaction of ketene methyl tert-butyldimethylsilyl acetal (1a) with the N-benzylnitrone (4a) prod

Ketene Silyl Acetal Chemistry; Diastereofacial Selectivity of 1,3-Addition of Chiral Nitrones

The reaction of dimethyl-t-butylsiloxy-1-methoxyethene (1a) with the N-benzylnitrone (3a) produced the syn-1,3-adduct (4a) predominantly, while the reaction of dimethyl-t-butylsiloxy-1-t-butoxyethene (1b) with the N-diphenylmethylnitrone (3d) gave the ant