Relevant bibliographies by topics / Arylnaphthalene lignan

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Academic literature on the topic 'Arylnaphthalene lignan'

Author: Grafiati
Published: 4 June 2021
Last updated: 5 February 2022

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Journal articles on the topic "Arylnaphthalene lignan"

1

Cow, Christopher, Carmen Leung, and James L. Charlton. "Antiviral activity of arylnaphthalene and aryldihydronaphthalene lignans." Canadian Journal of Chemistry 78, no. 5 (2000): 553–61. http://dx.doi.org/10.1139/v00-059.

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A practical method for large scale synthesis of 1-arylnaphthalene and 1-aryl-1,2-dihydronaphthalene lignans is described. The method makes use of the classic Stobbe condensation followed by regioselective reactions that provide access to both the common and retrolactone lignans, e.g., 2 and 3. A total of 25 compounds, many of which are known natural products, were prepared and their antiviral activity against human cytomegalovirus measured.Key words: lignan, Stobbe, arylnaphthalene, antiviral.
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2

Ivanova, Antoaneta, Bozhanka Mikhova, Tatyana Stambolijska, and Ivanka Kostova. "Lignan and Coumarin Glycosides from Haplophyllum suaveolens." Zeitschrift für Naturforschung C 56, no. 5-6 (2001): 329–33. http://dx.doi.org/10.1515/znc-2001-5-602.

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Two new lignan glycosides of dibenzylbutyrolactol type (haplomarin) and arylnaphthalene type (haploborin) were isolated from the aerial parts of Haplophyllum suaveolens together with the known arylnaphthalene lignan glycoside arabelline and hydroxycoumarin glycoside xeroboside. So far arabelline is found only in H. buxbaumii. This is the first report of the isolation of xeroboside from Haplophyllum.
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3

Meng, Jin, Liyue Du, and Liucheng Guo. "Synthesis of Arylnaphthalene Lignan Lactones." Chinese Journal of Organic Chemistry 36, no. 11 (2016): 2723. http://dx.doi.org/10.6023/cjoc201603007.

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4

Das, B., and J. Banerji. "Arylnaphthalene lignan from Jatropha gossypifolia." Phytochemistry 27, no. 11 (1988): 3684–86. http://dx.doi.org/10.1016/0031-9422(88)80799-4.

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5

Xiao, Jian, Guangming Nan, Ya-Wen Wang та Yu Peng. "Concise Synthesis of (+)-β- and γ-Apopicropodophyllins, and Dehydrodesoxypodophyllotoxin". Molecules 23, № 11 (2018): 3037. http://dx.doi.org/10.3390/molecules23113037.

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Herein, we present an expeditous synthesis of bioactive aryldihydronaphthalene lignans (+)-β- and γ-apopicropodophyllins, and arylnaphthalene lignan dehydrodesoxypodophyllotoxin. The key reaction is regiocontrolled oxidations of stereodivergent aryltetralin lactones, which were easily accessed from a nickel-catalyzed reductive cascade approach developed in our group.
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6

Al-Abed, Yousef, Musa Abu-Zarga, Salim Sabri, Atta-Ur-Rahman, and Wolfgang Voelter. "A arylnaphthalene lignan from Haplophyllum buxbaumii." Phytochemistry 49, no. 6 (1998): 1779–81. http://dx.doi.org/10.1016/s0031-9422(98)00222-2.

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7

NAVARRO, Eduardo, Simeona Josefina ALONSO, Pedro Juan ALONSO, Juan TRUJILLO, Elena JORGE, and Cirilo PEREZ. "Pharmacological Effects of Elenoside, an Arylnaphthalene Lignan." Biological & Pharmaceutical Bulletin 24, no. 3 (2001): 254–58. http://dx.doi.org/10.1248/bpb.24.254.

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8

Ogiku, Tsuyoshi, Shin-ichi Yoshida, Tooru Kuroda, Hiroshi Ohmizu, and Tameo Iwasaki. "A New Synthesis of Arylnaphthalene Lignan Lactones." Synlett 1992, no. 08 (1992): 651–52. http://dx.doi.org/10.1055/s-1992-21444.

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9

Hesse, Manfred, Belkis Gozler, Gokay Arar, and Tekant Gozler. "Isodaurinol, an arylnaphthalene lignan from Haplophyllum cappadocicum." Phytochemistry 31, no. 7 (1992): 2473–75. http://dx.doi.org/10.1016/0031-9422(92)83302-f.

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10

Rangkaew, Noppadon, Rutt Suttisri, Masataka Moriyasu, and Kazuko Kawanishi. "A new arylnaphthalene lignan from Knema furfuracea." Fitoterapia 80, no. 6 (2009): 377–79. http://dx.doi.org/10.1016/j.fitote.2009.05.005.

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