Hydrocinnamaldehyde Explained

Hydrocinnamaldehyde is the organic compound with the formula C6H5CH2CH2CHO. It is produced by the hydrogenation of cinnamaldehyde. The compound is used in many mechanistic studies.[1] It is a common substrate in organic synthesis.[2] [3]

References

  1. 10.1126/science.1120560. Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Au-Pd/TiO2 Catalysts. 2006. Enache. Dan I.. Edwards. Jennifer K.. Landon. Philip. Solsona-Espriu. Benjamin. Carley. Albert F.. Herzing. Andrew A.. Watanabe. Masashi. Kiely. Christopher J.. Knight. David W.. Hutchings. Graham J.. Science. 311. 5759. 362–365. 16424335. 2006Sci...311..362E. 92890.
  2. Hiroaki. Sasai. Shizue. Watanabe. Takeyuki. Suzuki. Masakatsu. Shibasaki. 10.15227/orgsyn.078.0014. Catalytic Asymmetric Synthesis of Nitroaldols Using a Lanthanum-Lithium-Binol Complex: (2S,3S)-2-Nitro-5-Phenyl-1,3-Pentanediol. Organic Syntheses. 2002. 78. 14.
  3. 10.15227/orgsyn.092.0038. Enantioselective Reductive Syn-Aldol Reactions of 4-Acryloylmorpholine: Preparation of (2R, 3S)-3-Hydroxy-2-methyl-1-morpholino-5-phenylpentan-1-one. 2015. Abbott. Jason. Christophe. Allais. William R.. Roush. Organic Syntheses. 92. 38–57.

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