936628-41-0

Upstream product

• 936628-38-5 (E)-1-{(2R)-1-[(1R)-1-phenylethyl]-aziridin-2-yl}-2-buten-1-one 
• 936628-37-4 {2-oxo-2-[(2R)-1-(1R)-(1-phenylethyl)-aziridin-2-yl]ethyl}-phosphonic acid dimethyl ester 
• 68820-82-6 (2R)-1[(R)-α-methylbenzyl]-2-aziridinecarboxylate ethyl ester 
• 936628-48-7 1-{(2R)-1-[(1R)-1-phenylethyl]-aziridine}-2-carboxylic acid methoxy methyl amide 
• 1278522-23-8 1-{(R)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-yn-1-one 
• 1204694-63-2 (R)-1-{(R)-1-[(R)-1-phenylethyl]aziridin-2-yl}but-2-yn-1-ol 

Downstream Products

• 936628-45-4 (2S,3R,4E)-2-[(1R)-1-phenylethylamino]-1-phenylsulfanyl-4-hexen-3-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 
• 1278522-26-1 (2R,3R,E)-3-(t-butyldimethylsilyloxy)-2-[(R)-1-phenylethylamino]hex-4-enyl acetate 
• 1278522-24-9 (R)-2-[(R,E)-1-(t-butyldimethylsilyloxy)but-2-enyl]-1-[(R)-1-phenylethyl]aziridine 
• 936628-46-5 (2S,3R,4E)-2-[allyl-((1R)-1-phenylethyl)amino]-1-phenylsulfanyl-4-hexen-3-ol 

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.

Syntheses of tetrahydropyridin-3-ol and tetrahydroazepin-3-ol from a chiral aziridine-2-carboxylate

A method for the stereoselective preparation of 1,2,3,6-tetrahydropyridin-3-ols and 2,3,4,7-tetrahydro-1H-azepin-3-ols, potentially versatile intermediates in the asymmetric synthesis of various piperidine alkaloids and azasugars, has been developed. The