884498-59-3

Upstream product

• 853056-96-9 N-[(R)-α-methylbenzyl]-(2S)-aziridine-(N'-methoxy-N'-methyl)carboxamide 
• 105563-08-4 1-pentadecynyllithium 
• 765-13-9 pentadec-1-yne 
• 68820-72-4 (2S)-1-[(R)-α-methylbenzyl]-2-aziridinecarboxylate ethyl ester 
• 397849-98-8 N-[(R)-(+)-α-methylbenzyl]aziridine-2-(S)-carboxylic acid menthyl ester 

Downstream Products

• 1345009-54-2 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(2-phenylacetyl)oxazolidin-2-one 
• 1345009-57-5 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(4-nitrobenzoyl)-oxazolidin-2-one 
• 1345009-56-4 (S)-4-[(R,E)-1-hydroxyhexadec-2-enyl]-3-(2-methoxybenzoyl)oxazolidin-2-one 
• 884498-57-1 (S)-3-benzoyl-4-[(R,E)-1-hydroxyhexadec-2-enyl]oxazolidin-2-one 
• 884498-60-6 (R)-1-{(S)-1-[(R)-1-phenylethyl]aziridin-2-yl}hexadec-2-yn-1-ol 
• 884498-61-7 (E,2S,3R)-2-[(R)-1-phenylethylamino]-3-(t-butyldimethylsilyloxy)octadec-4-enyl acetate 
• 884498-64-0 (E)-(2S,3R)-3-(tert-Butyl-dimethyl-silanyloxy)-2-((R)-1-phenyl-ethylamino)-octadec-4-en-1-ol 

Relevant academic research and scientific papers

3,4-Disubstituted oxazolidin-2-ones as constrained ceramide analogs with anticancer activities

Heterocyclic analogs of ceramide as 3-alkanoyl or benzoyl-4-(1-hydroxy-2- enyl)-oxazolidin-2-ones were designed by binding of primary alcohol and amide in sphinogosine backbone as a carbamate. They were synthesized by addition of acyl halide to the common

Synthesis of constrained ceramide analogs and their potent antileukemic activities

Constrained ceramide analogs were designed and synthesized by binding terminal alcohol and amine of ceramide with additional carbonyl functional group as 3-acetyl (3), 3-propionyl (4), 3-benzoyl (5), and 3-hexadecanoyl-4-(1- hydroxyhexadec-2-enyl)-oxazoli

Efficient synthesis of enantiomerically pure 2-acylaziridines: Facile syntheses of N-Boc-safingol, N-Boc-D-erythro-sphinganine, and N-Boc-spisulosine from a common intermediate

Various enantiomerically pure 2-acylaziridines were prepared efficiently from the corresponding aziridine-2-carboxylate via Weinreb's amide and the subsequent treatment of organometallic compounds. The carbonyl group of those 2-acylaziridines was stereose