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may be referred to as a norabietane due to the absence <strong>of</strong> the methyl group at C-4. Also<br />

present in the structure is a double bond at ∆ 4 .<br />

19<br />

9<br />

H<br />

H<br />

H<br />

COOH<br />

H<br />

COOH<br />

H<br />

(19) abietic acid (20) levopimaric acid (21) ferruginol<br />

HO<br />

O<br />

10<br />

O<br />

H<br />

O<br />

OH<br />

7<br />

H<br />

O<br />

H<br />

α<br />

9<br />

β 8<br />

(22) carnosol (23) callicarpone (24) royleanone<br />

O<br />

O<br />

16<br />

15<br />

(25) tanshinone (26) dl-fichtelite<br />

H<br />

Figure 4: Representative structures <strong>of</strong> the different types <strong>of</strong> abietane diterpenoids<br />

(Nakanishi et al., 1974)<br />

The terms “nor”, “abeo” <strong>and</strong> “seco” are used widely in the abietanes. The use <strong>of</strong> “nor”<br />

occurs when a methyl group is eliminated from the structure. The number preceding<br />

“nor” refers to the carbon atom which has been eliminated. The prefix “abeo” is used<br />

12<br />

H<br />

O<br />

O<br />

15<br />

OH<br />

20<br />

O<br />

10<br />

7<br />

OH<br />

OH<br />

O<br />

6

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