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Dictymal, a new Seco-fusicoccin type diterpene from the brown alga dictyota dichotoma

✍ Scribed by Makoto Segawa; Nobuyasu Enoki; Mitsuhiko Ikura; Kunio Hikichi; Ryoichi Ishida; Haruhisa Shirahama; Takeshi Matsumoto


Publisher
Elsevier Science
Year
1987
Tongue
French
Weight
115 KB
Volume
28
Category
Article
ISSN
0040-4039

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✦ Synopsis


tified 20th carbon, C-6. Therefore, through the 'H assignments, the carbon skelton was given and the planner structure of ,$, was established. Relative stereochemistries of both rings were determined by the NOES observed with respect to those five pairs of protons, (H-l, H-3), (H-l, Me-19), (H-3, Me-19), (H-8, Me-20) and . Dictymal was considered to be biogenetically derived from epoxydictymene (x)6 which was also found in the same alga. The stereochemistry of dictymal should be represented as formula A7. Ha I C+ I5 Hb k


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Structure of epoxydictymene (l), a new tetracyclic diterpene from Dictyota dichotoma, has been determined zainly on the basis of X-ray analysis.

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A phytochemical investigation of a Mediterranean brown alga (Dictyota sp.) led to the isolation of a novel C 40 bis-diterpene, named dictyotadimer A. The chemical structure of this unusual dissymmetric dimer, characterized by a C-C linkage between two different xenicane units, was elucidated by 1D a

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Contrnued investrgatron of the manne brown alga, D/ctyofa vo/ub//~s, has led to the isolation of SIX new hydroazulenord, 1-6, and five previously reported drterpenes, 7-11 Each of the new compounds IS unusual n either the degree of oxygenation and, or the substitution pattern of the hydroazulenord r