@article{
 title = {New bibenzyl cannabinoid from the New Zealand liverwort Radula marginata.},
 type = {article},
 year = {2002},
 identifiers = {[object Object]},
 keywords = {- and liquid chromatogra-,-ms analysis,as resolution of the,bibenzyl,cannabinoid,chemosystematic study of the,chemosystematics,gc,lc,liver-,liverwort,phy,radula,relationships be-,we are continuing the,worts by gas chromatography},
 pages = {1390-1392},
 volume = {50},
 id = {db9b6bdc-05b1-34c3-928c-b37ba0c3b44b},
 created = {2017-04-05T23:02:08.713Z},
 file_attached = {true},
 profile_id = {6c9edcaf-81dc-3357-bb56-dee7616baa0c},
 group_id = {4cb6f261-be0d-3474-9ccf-7abee0d15aec},
 last_modified = {2017-04-24T01:39:42.934Z},
 read = {true},
 starred = {false},
 authored = {false},
 confirmed = {true},
 hidden = {false},
 folder_uuids = {86b25ccd-1760-445e-84f3-6598c5894d7a},
 private_publication = {false},
 abstract = {The ether extract of the New Zealand liverwort Radula marginata afforded a new cannabinoid type bibenzyl compound named perrottetinenic acid, and two new bibenzyls, together with a known cannabinoid, perrottetinene. Their structures were established by two dimensional (2D) NMR spectral data. The structure of perrottetinenic acid was a similar to that of Delta(1)-tetrahydrocannabinol, a known hallucinogen. Cannabinoid type bibenzyls have been isolated from liverwort Radula perrottetii, though have not previously been reported from the liverwort R. marginata.},
 bibtype = {article},
 author = {Toyota, Masao and Shimamura, Takuji and Ishii, Hikari and Renner, Matt and Braggins, John and Asakawa, Yoshinori},
 journal = {Chemical & pharmaceutical bulletin},
 number = {10}
}

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