Abstract
The first total synthesis of the racemic title compound is described. 3-Hydroxy-4-methyl acetophenone was used as the starting material and transformed into the target molecule in six steps. Synthetic turmeronol A displays spectral properties similar to those reported for the natural compound leading to confirmation of the proposed structure.
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Hudlicky T, Sinai-Zingde G and Natchus M G 1987Tetrahedron Lett. 28 5287
Imai S, Hayakawa Y, Seto H, Morikiyo M and Furihata K 1990Agric. Biol. Chem. 54 2367
McOmie J F W, Watts M L and West D E 1968Tetrahedron 24 2289
Mingos P, Michael D and Baghurst D R 1991Chem. Soc. Rev. 20 1
Vig O P, Bari S S, Sharma A and Sattar M A 1990Indian J. Chem. B29 284
Villieras J and Rambaud M 1983Synthesis 300
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Sharma, M.L., Chand, T. Synthesis of (±)-2-methyl-6-(3′-hydroxy-4′-methylphenyl)-2-hepten-4-one [turmeronol A]. Proc. Indian Acad. Sci. (Chem. Sci.) 109, 177–180 (1997). https://doi.org/10.1007/BF02883487
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DOI: https://doi.org/10.1007/BF02883487