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. 2014 Jul 15;5:346. doi: 10.3389/fmicb.2014.00346

Figure 1.

Figure 1

Selected monoterpene transformations. (A) (+)-camphor [1] hydroxlation to 5-hydroxycamphor [2]; (B) 1,8-cineole [10] hydroxylation to hydroxy-1,8-cineole [11]; (C) α-pinene [3] epoxidation to α-pinene oxide [5]; (D) (R)-limonene [6] hydroxylation to perillyl alcohol [15]; (E) myrcene [25] hydration to (S)-(+)-linalool [17] and isomerization to geraniol [24].