Chemistry:Hydrocinnamaldehyde
From HandWiki
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]
It is used in flavours and fragrances for its "fresh, cortex, green, leafy, foliage, balsamic, storax, aldehydic, floral, melon" aroma.[4]
References
- ↑ Enache, Dan I.; Edwards, Jennifer K.; Landon, Philip; Solsona-Espriu, Benjamin; Carley, Albert F.; Herzing, Andrew A.; Watanabe, Masashi; Kiely, Christopher J. et al. (2006). "Solvent-Free Oxidation of Primary Alcohols to Aldehydes Using Au-Pd/TiO2 Catalysts". Science 311 (5759): 362–365. doi:10.1126/science.1120560. PMID 16424335. Bibcode: 2006Sci...311..362E.
- ↑ Sasai, Hiroaki; Watanabe, Shizue; Suzuki, Takeyuki; Shibasaki, Masakatsu (2002). "Catalytic Asymmetric Synthesis of Nitroaldols Using a Lanthanum-Lithium-Binol Complex: (2S,3S)-2-Nitro-5-Phenyl-1,3-Pentanediol". Organic Syntheses 78: 14. doi:10.15227/orgsyn.078.0014.
- ↑ Abbott, Jason; Allais, Christophe; Roush, William R. (2015). "Enantioselective Reductive Syn-Aldol Reactions of 4-Acryloylmorpholine: Preparation of (2R, 3S)-3-Hydroxy-2-methyl-1-morpholino-5-phenylpentan-1-one". Organic Syntheses 92: 38–57. doi:10.15227/orgsyn.092.0038.
- ↑ "3-phenyl propionaldehyde". Scents and Flavors. https://scentsandflavors.com/database/9dbb500a-8d77-4494-8b2e-ef6deead4194.
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