1987
DOI: 10.1016/s0031-9422(00)81855-5
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Malabaricane derivatives from Pyrethrum santolinoides

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Cited by 36 publications
(15 citation statements)
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“…Malabaricanediol, a precursor of malabaricol, is structurally consistent with cyclization from 2,3-epoxy-18,19-dihydrosqualene-18,19-diol. Later, Bohlmann et al isolated malabarica-14(27),17,21-trien-3-ol (B) [20] and an aqua-quenched product (C) has been generated in the laboratory. Incidentally, it may be mentioned that isomalabaricane has been isolated from a sea sponge [21].…”
Section: Tricyclic Triterpenesmentioning
confidence: 99%
“…Malabaricanediol, a precursor of malabaricol, is structurally consistent with cyclization from 2,3-epoxy-18,19-dihydrosqualene-18,19-diol. Later, Bohlmann et al isolated malabarica-14(27),17,21-trien-3-ol (B) [20] and an aqua-quenched product (C) has been generated in the laboratory. Incidentally, it may be mentioned that isomalabaricane has been isolated from a sea sponge [21].…”
Section: Tricyclic Triterpenesmentioning
confidence: 99%
“…(Abdel-Mogib et al, 1989). The roots of this last species afforded rare and unusual triterpenes, specifically two further representatives of the rare type of malabaricanetriterpenes (Jakupovic et al, 1987).…”
Section: ~~mentioning
confidence: 99%
“…The structures of the remaining sodagnitins B (2) and Pyrethrum santolinoides [9] and from two marine 23 24.8 q 25.1 q 28.6 q sponges. [10,11] The sodagnitins differ from these compounds [a] Multiplicities determined by DEPT sequences The sodagnitins are colourless, amorphous powders which can be kept for several months at room temperature.…”
Section: Elucidationmentioning
confidence: 99%