1987
DOI: 10.1016/s0031-9422(00)82380-8
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(7R)-Transtrans-nepetalactone from Nepeta elliptica

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Cited by 32 publications
(10 citation statements)
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“…Therefore, the structures and relative configurations of 1 and 2 are 13,6a-dihydroxyand lß,6ß-dihydroxy-7-e/u-eudesm-4(15)-ene, respectively. The 13C-and 'H-nmr data of ßeudesmol and -cadinol, also isolated in this investigation, were identical with published data (18,19).…”
supporting
confidence: 87%
“…Therefore, the structures and relative configurations of 1 and 2 are 13,6a-dihydroxyand lß,6ß-dihydroxy-7-e/u-eudesm-4(15)-ene, respectively. The 13C-and 'H-nmr data of ßeudesmol and -cadinol, also isolated in this investigation, were identical with published data (18,19).…”
supporting
confidence: 87%
“…Some species of this genus are important medical plants and they have euphoric effects on cats [2]. Many species of the genus have been investigated and found to contain monoterpenoids, diterpenoids and triterpenoids [3][4][5] N. cataria L. (catnip), the most thoroughly studied species, is used in folk medicine as diuretic, carminative, antispasmodic, emmenagogue and sedative [6,7]. N. argolica Bory et chaub.…”
mentioning
confidence: 99%
“…6,8,17 Many Nepeta spp. contain the diasteromeric nepetalactones, substituted cyclopentanoid iridodial derivatives.…”
mentioning
confidence: 99%