“…These spectral data suggested the presence of a halimane diterpenoid skeleton with a β-substituted furan ring in 1. The 13 C-NMR spectrum was similar to chettaphanin I (2), 9,16 except for the lack of a C-12 keto carbonyl group, instead of the presence of olefinic carbons at 142.3 (C-11), and 130.2 (C-12). The HMBC spectrum also showed correlations between H-11 and C-1, C-8, C-9, C-10, suggested that the presence of a cyclopentadiene ring formed by C-9, C-10, C-1, C-12 and C-11 in 1.…”