1999
DOI: 10.1016/s0031-9422(98)00464-6
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Isolation and synthesis of a new clerodane from Echinodorus grandiflorus

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Cited by 42 publications
(29 citation statements)
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“…A strong IR absorption band occurred at 3434 cm -1 . The molecular formula, C 21 H 30 O 5 (HRESIMS), was consistent with this proposal. One of the hydroxyl groups was again located at C-1, showing the same couplings as in 7.…”
supporting
confidence: 85%
“…A strong IR absorption band occurred at 3434 cm -1 . The molecular formula, C 21 H 30 O 5 (HRESIMS), was consistent with this proposal. One of the hydroxyl groups was again located at C-1, showing the same couplings as in 7.…”
supporting
confidence: 85%
“…Substâncias terpenoídicas das quais destacamse diterpenos dos tipos clerodano (Costa et al, 1999;Tanaka, 2000) e cembrano tais como equinodol (Manns;Hartman, 1993) e ácido equinóico (Tanaka et al, 1997, Tanaka, 2000 foram isoladas de E. grandifl orus. Os diterpenos equinofi linas A e B (Kobayashi et al, 2000) e equinodolidos A e B (Shigemori et al, 2002) foram identifi cados em E. macrophyllus.…”
Section: Introductionunclassified
“…The pro-19S diastereotopic proton, which was ω-coupled ( 4 J = 2.0 Hz) with H-6β, 23 showed correlations with H-1α and H 3 -20, indicating α-and axial orientation for both C-20 and C-19. In addition, the axially 24 except that a methoxy group was evident in 6. HMBC correlation in 6 from the methoxy protons (δ H 3.57) to C-16 verified that the methoxy group was at C-16.…”
Section: Resultsmentioning
confidence: 99%