53910-44-4

Upstream product

• 53910-43-3 Benzyl-2-acetylamino-3-amino-4,6-O-benzyliden-2,3-didesoxy-α-D-glucopyranosid 
• 27539-63-5 Benzyl-2-acetylamino-3-azido-4,6-O-benzyliden-2,3-didesoxy-α-D-glucopyranosid 
• 78153-46-5 Benzyl-2,3-diamino-4,6-O-benzyliden-2,3-didesoxy-2,3-N-oxalyl-α-D-glucopyranosid 

Downstream Products

• 78153-48-7 Benzyl-2,3-diamino-2,3-didesoxy-2,3-N-oxalyl-α-D-glucopyranosid 
• 78153-54-5 Benzyl-2-amino-4,6-O-benzyliden-3-(carboxycarbonylamino)-2,3-didesoxy-α-D-glucopyranosid 
• 78153-57-8 Benzyl-4,6-di-O-acetyl-2-acetylamino-2,3-didesoxy-3-(methoxalylamino)-α-D-glucopyranosid 
• 78153-56-7 Benzyl-4,6-di-O-acetyl-2-acetylamino-2,3-didesoxy-3-(ethoxalylamino)-α-D-glucopyranosid 
• 78153-50-1 Benzyl-2,3-diamino-2,3-di-N-benzoyl-4,6-di-O-benzoyl-2,3-didesoxy-2,3-N-oxalyl-α-D-glucopyranosid 
• 78153-47-6 Benzyl-4,6-O-benzyliden-2,3-didesoxy-2,3-bis(ethoxymalonylamino)-α-D-glucopyranosid 
• 78153-46-5 Benzyl-2,3-diamino-4,6-O-benzyliden-2,3-didesoxy-2,3-N-oxalyl-α-D-glucopyranosid 

Relevant academic research and scientific papers

Di- und Polyaminozucker, XXIV. Synthese und Reaktionen der 2,3-Diamino-2,3-didesoxy-2,3-N-oxalyl-D-glucose

On reaction with diethyl oxalate benzyl 2,3-diamino-4,6-O-benzylidene-2,3-dideoxy-α-D-glucopyranoside (3) cyclised to the 2,3-oxamide 4 which was deblocked to give the title compound 9.Complete hydrolysis of the oxamide (-> 3) occurred on reaction with alkali.Under acetylating conditions only ring fission took place to give N-oxalyl derivatives (11, 13, 14, 16 - 19).