901265-41-6

Upstream product

• 13135-58-5 C₁₀H₁₉NO₂ 
• 501-53-1 benzyl chloroformate 
• 630-19-3 pivalaldehyde 
• 72-18-4 L-valine 

Downstream Products

• 1033081-67-2 C₁₉H₂₇NO₄ 
• 901265-52-9 (4R)-3-[2-(tert-butyl-dimethylsilanyloxy)-3-phenylsulfanyl-propionyl]-4-isopropyl-2-oxo-oxazolidine-4-carboxylic acid benzyl ester 
• 901266-67-9 (2S,4R)-3-[2-(tert-butyl-dimethylsilanyloxy)-3-phenylsulfanyl-propionyl]-4-isopropyl-2-oxo-oxazolidine-4-carboxylic acid benzyl ester 
• 901266-05-5 (6S,8αR)-6-benzenesulfinylmethyl-8α-isopropyl-dihydro-oxazolo[4,3-c]-[1,4]oxazine-3,5,8-trione 
• 901265-45-0 (2S,4S)-2-tert-butyl-4-hydroxymethyl-4-isopropyl-5-oxo-oxazolidine-3-carboxylic acid benzyl ester 
• 901265-26-7 (8αR)-8α-isopropyl-6-phenylsulfanylmethyl-dihydro-oxazolo[4,3-c]-[1,4]oxazine-3,5,8-trione 
• 901266-71-5 (6S,8αR)-8α-isopropyl-6-phenylsulfanylmethyl-dihydro-oxazolo[4,3-c]-[1,4]oxazine-3,5,8-trione 
• 901265-34-7 (4R)-4-isopropyl-2-oxo-oxazolidine-4-carboxylic acid benzyl ester 
• 901265-97-2 (2S,4S)-2-tert-butyl-4-isopropyl-4-(4-methoxy-benzyloxymethyl)-5-oxo-oxazolidine-3-carboxylic acid benzyl ester 

Relevant academic research and scientific papers

Enantioselective synthesis and enantiomeric amplification of amino acids under prebiotic conditions

(Chemical Equation Presented) A plausible origin of biomolecular homochirality is advanced, where α-methyl amino acids found on meteorites transfer their chirality in the synthesis of normal amino acids. This asymmetry can be amplified to nearly homochiral levels, thus providing the necessary prerequisite for life to start on this planet and elsewhere in the universe.

Synthesis of precursors of the agalacto (exo) fragment of the quartromicins via an auxiliary-controlled exo-selective Diels-Alder reaction

A direct synthesis of the α-hydroxyaldehyde exo-5, a precursor of the exo-spirotetronate subunit of the quartromicins, was achieved through an exo-selective Lewis acid-catalyzed Diels-Alder reaction of dienophile 12a and diene 1.