112635-79-7

Upstream product

• 94-02-0 ethyl 3-oxo-3-phenylpropionate 
• 112635-77-5 ethyl (S)-(-)-3-(tert-butyldimethylsilyloxy)-3-phenylpropanoate 
• 33401-74-0 ethyl (3R)-3-hydroxy-3-phenylpropionate 
• 167642-19-5 (S)-(-)-4-nitro-1-phenyl-1-butanol 
• 167642-26-4 (S)-(-)-1-(dimethyl-t-butylsilyloxy)-4-nitro-1-phenylbutane 
• 18162-48-6 tert-butyldimethylsilyl chloride 
• 186581-53-3 diazomethane 
• 112635-78-6 (S)-(-)-3-(tert-butyldimethylsilyloxy)-3-phenylpropanoic acid 

Downstream Products

• 111138-02-4 (-)-(S)-5-phenyl-4,5-dihydrofuran-2(3H)-one 

Relevant academic research and scientific papers

Baker's yeast reduction of prochiral γ-nitroketones: Enantioselective synthesis of (S)-4-nitroalcohols

The baker's yeast reduction of seven different prochiral nitroketones 1a-g occurred on the re face of the carbonyl group, thus affording the (S)-nitroalcohols 2a-g, with different level of enantioselectivity (e.e. 15-99%). The best results (e.e. = 99%) we

Studies on the Stereochemical Control of Fermenting Baker's Yeast Mediated Reductions: Some 3- and 4-Oxo Esters

Ethyl 4-benzyloxy-3-oxobutanoate (1c) is reduced by fermenting baker's yeast with stereochemical control which is dependent on the yeast: substrate ratio and the presence or absence of ethanol.Contrary to earlier reports, ethyl levulinate (3a) can be ster