2000
DOI: 10.1039/a900251k
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β-Phenylethylamines and the isoquinoline alkaloids (July 1998 to June 1999)

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Cited by 41 publications
(12 citation statements)
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“…6-Hydroxy-5,6-dihydrobenzophenanthridines also yield dimerization products [130]. This reactivity was exemplified by easy conversion of chelilutine (321; Sanguinaria canadensis, Eschscholtzia californica, Papaveraceae) into 322-324 under basic conditions (Scheme 24.75) [132].…”
Section: Halogenated Solventsmentioning
confidence: 99%
See 1 more Smart Citation
“…6-Hydroxy-5,6-dihydrobenzophenanthridines also yield dimerization products [130]. This reactivity was exemplified by easy conversion of chelilutine (321; Sanguinaria canadensis, Eschscholtzia californica, Papaveraceae) into 322-324 under basic conditions (Scheme 24.75) [132].…”
Section: Halogenated Solventsmentioning
confidence: 99%
“…Prod. 2008, 71,[130][131][132][133] Ampelocissus sp., Vitaceae, root "This is not an acetogenin of Annonaceae" Possible or proven botanical misidentifications[3, 4].…”
mentioning
confidence: 99%
“…For details of the biological activities of isoquinolinone compounds, see: Bentley (2000); Jayaraman et al (2002). For the Bischler-Napieralski reaction, see: Bischler & Napieralski (1893).…”
Section: Related Literaturementioning
confidence: 99%
“…[5] Therefore, new methods for the synthesis of these targets are required. [6] Some heterocylic compounds that are fused with pyrimidines are well known for their different biological activities. [7][8][9][10] For example, many of pyrimidoquinoline and pyrimidoisoquinoline derivatives show biological activities such as anticancer, [11,12] anti-inflammatory, [13] antiallergic, [14] antimicrobial, [15,16] antibacterial, [17,18] antifungal, [19] antimalarial [20] and antifolate.…”
Section: Introductionmentioning
confidence: 99%