1418183-68-2

Upstream product

• 1418183-65-9 (S)-3-[(R)-2-ethylhexanoyl]-4-phenyloxazolidin-2-one 
• 1418183-64-8 O-(2R,3S)-3-[(S)-2-oxo-4-phenyloxazolidin-3-ylcarbonyl]heptan-2-yl O-phenyl carbonothioate 
• 1418183-63-7 (S)-3-{(S)-2-[(R)-1-hydroxyethyl]hexanoyl}-4-phenyloxazolidin-2-one 
• 1418183-62-6 (S)-3-hexanoyl-4-phenyloxazolidin-2-one 
• 142-62-1 hexanoic acid 
• 1418183-67-1 (R)-2-ethylhexyl (E)-3-[3-(benzyloxy)phenyl]acrylate 
• 50373-29-0 (R)-2-ethylhexanol 
• 122024-75-3 3-<3-(phenylmethoxy)phenyl>-2-propenoic acid 
• 208836-69-5 3-(3'-benzyloxyphenyl)-(E)-propenoic acid ethyl ester 

Relevant academic research and scientific papers

Synthesis of the structure proposed for natural meliloester

In an attempt to establish the absolute configuration of meliloester, a natural product isolated from Melilotus alba, the literature structure was synthesized in an enantiopure form. Unexpectedly, the 1H and 13C NMR data was completely incompatible with those reported for the natural product. The corresponding m-hydroxy isomer was also excluded as the structure for the natural product.