Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Heliparvifoline"'
Publikováno v:
Natural Product Letters. 1:269-272
The aerial parts of Haplophyllum thesioides yielded a new alkaloid, thenaptosine [4,5-dimethoxy-11-metriylfuro(2,3-c)acridin-6(15H)-on] and a new coumarin, thesiolen (4-methoxyangelicin) in addition to known alkaloids, kokusaginine, skimmianine, ptel
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6c5cbc9273c18882d6d6d97904ce1713
https://doi.org/10.1080/10575639308050059
https://doi.org/10.1080/10575639308050059
Publikováno v:
ChemInform. 27
A new phenolic furoquinoline alkaloid, evomerrine, was isolated from the leaves of Melicope semecarpifolia . Its structure was elucidated from spectral data and chemical evidence. Six other known furoquinoline alkaloids, platydesmine, skimmianine, ko
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb11099d08320d5bfa3e603ccb7957e7
https://doi.org/10.1002/chin.199613252
https://doi.org/10.1002/chin.199613252
Autor:
Sam Sik Kang, Won Sick Woo
Publikováno v:
Archives of Pharmacal Research. 9:11-13
In addition to the previous reported furoquinoline alkaloids, skimmianine, kokusaginine and confusameline, a rare furoquinoline alkaloid, heliparvifoline, mp 241-3°, was isolated from the leaves ofMelicope confusa and characterized by spectral data.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::46ac8d87bace21e1d2997d81ddb2bf8a
https://doi.org/10.1007/bf02857699
https://doi.org/10.1007/bf02857699
Autor:
G.H. Aynilian, Norman R. Farnsworth, M. Tin-Wa, Harry H. S. Fong, Geoffrey A. Cordell, R.E. Perdue, P.T.O. Chang
Publikováno v:
Journal of Pharmaceutical Sciences. 65:561-563
A phytochemical investigation of the leaves and twigs of Helietta parvifolia (Rutaceae) resulted in the isolation of heliparvifoline, a new furoquinoline alkaloid, in addition to the known bases flindersiamine and isoflindersiamine.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1036a2bc89f80044d20007fd233c819d
https://doi.org/10.1002/jps.2600650420
https://doi.org/10.1002/jps.2600650420
Akademický článek
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Autor:
Tetsuya Sekiba
Publikováno v:
Chemischer Informationsdienst. 9
2,3-Dihydroheliparvifoline (Va) was obtained from 4-methoxy-3-benzyloxyaniline by condensation with diethyl (2-benzyloxyethyl)-malonate, and by subsequent methylation, debenzylation, and then cyclodehydration. Benzyl ether of Va was dehydrogenated an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c39be8abf20809749b9de762b6b1fe9a
https://doi.org/10.1002/chin.197815235
https://doi.org/10.1002/chin.197815235
Akademický článek
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Publikováno v:
Scopus-Elsevier
A new phenolic furoquinoline alkaloid, evomerrine, was isolated from the leaves of Melicope semecarpifolia . Its structure was elucidated from spectral data and chemical evidence. Six other known furoquinoline alkaloids, platydesmine, skimmianine, ko
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2c81418b6d34f9157d36182a00ebc90
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028869915&partnerID=MN8TOARS
http://www.scopus.com/inward/record.url?eid=2-s2.0-0028869915&partnerID=MN8TOARS
Autor:
Tetsuya Sekiba
Publikováno v:
Bulletin of the Chemical Society of Japan. 51:325-326
2,3-Dihydroheliparvifoline (Va) was obtained from 4-methoxy-3-benzyloxyaniline by condensation with diethyl (2-benzyloxyethyl)-malonate, and by subsequent methylation, debenzylation, and then cyclodehydration. Benzyl ether of Va was dehydrogenated an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9362228d464f7d01306db8f187735995
https://doi.org/10.1246/bcsj.51.325
https://doi.org/10.1246/bcsj.51.325