1204694-63-2

Upstream product

• 68820-82-6 (2R)-1[(R)-α-methylbenzyl]-2-aziridinecarboxylate ethyl ester 
• 1278522-23-8 1-{(R)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-yn-1-one 
• 936628-48-7 1-{(2R)-1-[(1R)-1-phenylethyl]-aziridine}-2-carboxylic acid methoxy methyl amide 

Downstream Products

• 936628-41-0 (1R,2E)-1-{(2R)-1-[(1R)-1-phenylethyl]-aziridin-2-yl}-2-buten-1-ol 
• 1278522-28-3 (2R,3R,E)-3-(t-butyldimethylsilyloxy)-2-[(R)-1-phenylethylamino]hex-4-en-1-ol 
• 1278522-30-7 (R)-4-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]-3-[(R)-1-phenylethyl]oxazolidin-2-one 
• 1278522-24-9 (R)-2-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]-1-[(R)-1-phenylethyl]aziridine 
• 1278522-26-1 (2R,3R,E)-3-(t-butyldimethylsilyloxy)-2-[(R)-1-phenylethylamino]hex-4-enyl acetate 

Relevant academic research and scientific papers

Asymmetric synthesis of 1-deoxyazasugars from chiral aziridines

A general and facile synthesis of enantiopure 1-deoxyazasugars was achieved from stereoselective dihydroxylation of a common synthetic intermediate, piperidine ring fused oxazolidin-2-one, originating from a commercially available starting substrate, chiral aziridine-2-carboxylate, in high yields. The Royal Society of Chemistry 2011.