4 entries
Claim · model-written summary
Two new sesquiterpenoids were isolated from Gackstroemia species.
Verbatim
e0“Two new sesquiterpenoids, 1 and 2, were isolated from the unidentified liverwort Gackstroemia species”
Title
Fumihiro Nagashima; Yoshiaki Kuba; Atsushi Ogata; et al. Natural Product Research 2009. doi:10.1080/14786410902800749
Claim · model-written summary
Clavigerin A was the only clavigerin detected in a North Island collection of Lepidolaena clavigera.
Lepidolaena clavigerae1Verbatim
e1“Lepidolaena clavigera”
e2“1 was the only clavigerin detected in a North Island collection”
Title
Nigel B. Perry; Elaine J. Burgess; Lysa M. Foster; et al. Journal of Natural Products 2008. doi:10.1021/np070644l
Claim · model-written summary
Clavigerins B and C were found in South Island collections of Lepidolaena clavigera, with no sign of clavigerin A.
Lepidolaena clavigerae1Verbatim
e1“Lepidolaena clavigera”
e2“the previously reported clavigerins B ( 2) and C ( 3) were found in South Island collections with no sign of 1”
Title
Nigel B. Perry; Elaine J. Burgess; Lysa M. Foster; et al. Journal of Natural Products 2008. doi:10.1021/np070644l
Claim · model-written summary
Three new clavigerins, 4-6, were identified; they are artifacts formed by alcoholysis of clavigerins 2 and 3 with the extraction or eluent solvent.
Lepidolaena clavigerae1Verbatim
e1“Lepidolaena clavigera”
e2“Three new clavigerins, 4- 6, were identified, but these are artifacts formed by alcoholysis of the acetoxy acetal group of the clavigerins 2 and 3”
Title
Nigel B. Perry; Elaine J. Burgess; Lysa M. Foster; et al. Journal of Natural Products 2008. doi:10.1021/np070644l
Claim · model-written summary
The clavigerin artifacts are proposed to act as hidden 1,4-dicarbonyl compounds.
Lepidolaena clavigerat0Verbatim
t0“Lepidolaena clavigera”
e1“it is proposed that they act as hidden 1,4-dicarbonyl compounds”
Title
Nigel B. Perry; Elaine J. Burgess; Lysa M. Foster; et al. Journal of Natural Products 2008. doi:10.1021/np070644l
Claim · model-written summary
Hodgsonox was isolated as a new insecticidal sesquiterpene from Lepidolaena hodgsoniae.
Lepidogyna hodgsoniaee0Verbatim
e0“Hodgsonox (1), a new insecticidal sesquiterpene, has been isolated from the New Zealand liverwort Lepidolaena hodgsoniae”
Title
Gary D. Ainge; Philippa J. Gerard; Simon F. R. Hinkley; et al. The Journal of Organic Chemistry 2001. doi:10.1021/jo0017685
Claim · model-written summary
Hodgsonox has a cyclopenta[5,1-c]pyran ring fused to oxirane.
Lepidogyna hodgsoniaet0Verbatim
e0“Hodgsonox represents a new class of sesquiterpene with a cyclopenta[5,1-c]pyran ring system fused to an oxirane ring”
t0“Lepidolaena hodgsoniae”
Title
Gary D. Ainge; Philippa J. Gerard; Simon F. R. Hinkley; et al. The Journal of Organic Chemistry 2001. doi:10.1021/jo0017685
Claim · model-written summary
Its flanking double bond arrangement was reported as a unique structural feature.
Lepidogyna hodgsoniaet0Verbatim
e0“The combination of a mono- and a 1,1 disubstituted double bond flanking the oxygenated carbon of a the pyran ring is a unique structural feature”
t0“Lepidolaena hodgsoniae”
Title
Gary D. Ainge; Philippa J. Gerard; Simon F. R. Hinkley; et al. The Journal of Organic Chemistry 2001. doi:10.1021/jo0017685
Claim · model-written summary
Hodgsonox was toxic to Lucilia cuprina larvae.
Lepidogyna hodgsoniaet0Verbatim
e0“Hodgsonox is toxic to larvae of the blowfly Lucilia cuprina”
t0“Lepidolaena hodgsoniae”
Title
Gary D. Ainge; Philippa J. Gerard; Simon F. R. Hinkley; et al. The Journal of Organic Chemistry 2001. doi:10.1021/jo0017685
Claim · model-written summary
Two new diterpenoids were isolated from Lepidolaena clavigera and identified as highly oxygenated atisanes.
Lepidolaena clavigerae0Verbatim
e0“Two new diterpenoids were isolated from the New Zealand liverwort Lepidolaena clavigera. Spectroscopic studies identified the structures as atisanes 1 and 2, with an unprecedented level of oxygenation.”
Title
The First Atisane Diterpenoids from a Liverwort: Polyols from Lepidolaena clavigera
Nigel B. Perry; Elaine J. Burgess; Seung-Hwa Baek; et al. Organic Letters 2001. doi:10.1021/ol0169224