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(5R)-2-Methyl-5-(5-methyl-1-methylene-4-hexenyl)-2-cyclohexen-1-one synthesis

6synthesis methods
2244-16-8 Synthesis
D(+)-Carvone

2244-16-8
242 suppliers
$6.00/5g

-

Yield:-

Steps:

Multi-step reaction with 6 steps
1.1: 28.5 percent / NBS; benzoylperoxide / benzene / Heating
2.1: 2.54 g / LiAlH4
3.1: 740 mg / p-TsOH
4.1: Mg / tetrahydrofuran / -25 °C
4.2: 441 mg / cuprous bromide / tetrahydrofuran / 0.5 h / -25 °C
5.1: 320 mg / p-TsOH / ethanol
6.1: 130 mg / pyridinium dichlorochromate / dimethylformamide / 5 h / -10 °C

References:

Kim, Chul-Sa;Morisawa, Jun;Nishiyama, Nobuhiro;Kashiwagi, Takehiro;Tebayashi, Shin-Ich;Horiike, Michio [Bioscience, Biotechnology and Biochemistry,2002,vol. 66,# 9,p. 1997 - 2000]