900187-89-5

Upstream product

• 58561-04-9 N-tert-butoxycarbonyl-L-valine methyl ester 
• 100-39-0 benzyl bromide 
• 24424-99-5 di-tert-butyl dicarbonate 
• 40216-62-4 N-benzyl-L-valine methyl ester 
• 4070-48-8 L-Valine methyl ester 

Downstream Products

• 900187-76-0 tert-butyl benzyl(4-hydroxy-2-methylhex-5-en-3-yl)carbamate 
• 900187-77-1 3-benzyl-4-isopropyl-5-vinyloxazolidin-2-one 
• 399559-54-7 (S)-tert-butyl benzyl(3-methyl-1-oxobutan-2-yl)carbamate 
• 930117-66-1 ethyl (2E,4S)-4-[benzyl(tert-butoxycarbonyl)amino]-5-methylhex-2-enoate 
• 930117-68-3 tert-butyl benzyl[(1S,2E)-4-hydroxy-1-isopropylbut-2-enyl]carbamate 
• 930117-76-3 (4S,5R)-3-benzyl-4-isopropyl-2-oxooxazolidine-5-carboxylic acid 
• 900187-84-0 (2R,3S)-3-(benzylamino)-2-hydroxy-4-methylpentanoic acid 
• 930117-75-2 (4S,5S)-3-benzyl-4-isopropyl-5-vinyloxazolidin-2-one 
• 399559-62-7 tert-butyl benzyl[(1S)-1-(hydroxymethyl)-2-methylpropyl]carbamate 

Relevant academic research and scientific papers

Oxazolidinones and 2,5-Dihydrofurans via Zinc-Catalyzed Regioselective Allenylation Reactions of l -α-Amino Aldehydes

The simultaneous control of diastereoselectivity and regioselectivity in Zn-catalyzed allenylation reactions of N-protected l-α-amino aldehydes is reported. A reversal in diastereoselectivity could be realized by variation of the α-amino aldehyde protecti

Highly diastereoselective epimerization: Stereodivergent synthesis of α-hydroxy-β-amino isopentanoic acid

The high diastereoselectivity of the base-catalyzed epimerization of oxazolidin-2-ones 7 and 8 is shown to depend on the nature of the N-substituent (R group); when R = Bn, the 4,5-trans-product (4S,5R)-9 is formed, whereas when R = H the 4,5-cis-product