Acide orsellinique (French Wikipedia)

Analysis of information sources in references of the Wikipedia article "Acide orsellinique" in French language version.

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8doi.org

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5nih.gov

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1qmul.ac.uk

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1crcpress.com

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1alfa.com

7,745^th place

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1books.google.com

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1pnas.org

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1idw-online.de

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1actachemscand.org

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actachemscand.org

Klaus Mosbach, « Die Biosynthese der Orsellinsäure und Penicillinsäure (I) », Acta Chem. Scand., vol. 14,‎ 1960, p. 457–464 (lire en ligne)

alfa.com

« Fiche du composé 2,4-Dihydroxy-6-methylbenzoic acid hydrate », sur Alfa Aesar (consulté le 23 septembre 2020).

books.google.com

(de) R. Hegnauer, Chemotaxonomie der Pflanzen : Band 1: Thallophyten, Bryophyten; Pteridophyten und Gymnospermen, Bâle, Birkhäuser, 1962 (lire en ligne), p. 160

crcpress.com

(en) David R. Lide, CRC Handbook of Chemistry and Physics, Boca Raton, CRC Press/Taylor & Francis, 3 juin 2009, 90^e éd., 2804 p. (ISBN 9781420090840, présentation en ligne), p. 182

doi.org

dx.doi.org

Russell, R. et C Kemmelmeier, « Neutral, alkaline and difference ultraviolet spectra of secondary metabolites from Penicillium and other fungi, and comparisons to published maxima from gradient high-performance liquid chromatography with diode-array detection. », Journal of Chromatography, vol. 511,‎ 1990, p. 195–221 (PMID 2211911, DOI 10.1016/S0021-9673(01)93285-6)
Volker Schroeckh, Kirstin Scherlach, Hans-Wilhelm Nützmann, Ekaterina Shelest, Wolfgang Schmidt-Heck, Julia Schuemann, Karin Martin, Christian Hertweck, Axel A. Brakhage, « Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans », Proceedings of the National Academy of Sciences of the United States of America, vol. 106, n^o 34,‎ 2009, p. 14558–14563 (DOI 10.1073/pnas.0901870106}, lire en ligne)
James F. Sanchez, Yi-Ming Chiang, Edyta Szewczyk, Ashley D. Davidson, Manmeet Ahuja, C. Elizabeth Oakley, Jin Woo Bok, Nancy Keller, Berl R. Oakley, Clay C. C. Wang, « Molecular genetic analysis of the orsellinic acid/F9775 gene cluster of Aspergillus nidulans », Mol Biosyst., vol. 6, n^o 3,‎ 2010, p. 587–593 (PMID 20174687, PMCID 2903553, DOI 10.1039/B904541D)
Krystyna Nahlik, Marc Dumkow, Özgür Bayram, Kerstin Helmstaedt, Silke Busch, Oliver Valerius, Jennifer Gerke, Michael Hoppert, Elke Schwier, Lennart Opitz, Mieke Westermann, Stephanie Grond, Kirstin Feussner, Cornelia Goebel, Alexander Kaever, Peter Meinecke, Ivo Feussner, Gerhard H. Braus, « The COP9 signalosome mediates transcriptional and metabolic response for hormones, oxidative stress protection and cell wall rearrangement during fungal development », Molecular Microbiology, vol. 78, n^o 4,‎ 2010, p. 964–979 (DOI 10.1111/j.1365-2958.2010.07384.x)
G. W. Eijk, « Isolation and identification of orsellinic acid and penicillic acid produced by Penicillium fennelliae Stolk », Antonie van Leeuwenhoek, vol. 35, n^o 1,‎ 1969, p. 497–504 (DOI 10.1007/BF02219167)
Klaus Mosbach, « Die Rolle der Malonsäure in der Biosynthese der Orsellinsäure », Naturwissenschaften, vol. 48, n^o 15,‎ 1961, p. 525–525 (DOI 10.1007/BF00595346)
Kang, Ying, Mei, Yan, Du, Yuguo et Jin, Zhendong, « Total Synthesis of the Highly Potent Anti-HIV Natural Product Daurichromenic Acid along with Its Two Chromane Derivatives, Rhododaurichromanic Acids A and B », Organic Letters, vol. 5, n^o 23,‎ 2003, p. 4481–4484 (PMID 14602030, DOI 10.1021/ol030109m)
Kurt Hoesch, « Synthese der Orsellinsäure und der Everninsäure », Berichte der deutschen chemischen Gesellschaft, vol. 46, n^o 1,‎ 1913, p. 886–892 (DOI 10.1002/cber.191304601116)

idw-online.de

Michael Ramm : Bakterien induzieren Wirkstoffsynthese in Pilzen. Leibniz-Institut für Naturstoff-Forschung und Infektionsbiologie - Hans-Knöll-Institut (HKI)

nih.gov

ncbi.nlm.nih.gov

Russell, R. et C Kemmelmeier, « Neutral, alkaline and difference ultraviolet spectra of secondary metabolites from Penicillium and other fungi, and comparisons to published maxima from gradient high-performance liquid chromatography with diode-array detection. », Journal of Chromatography, vol. 511,‎ 1990, p. 195–221 (PMID 2211911, DOI 10.1016/S0021-9673(01)93285-6)
James F. Sanchez, Yi-Ming Chiang, Edyta Szewczyk, Ashley D. Davidson, Manmeet Ahuja, C. Elizabeth Oakley, Jin Woo Bok, Nancy Keller, Berl R. Oakley, Clay C. C. Wang, « Molecular genetic analysis of the orsellinic acid/F9775 gene cluster of Aspergillus nidulans », Mol Biosyst., vol. 6, n^o 3,‎ 2010, p. 587–593 (PMID 20174687, PMCID 2903553, DOI 10.1039/B904541D)
Kang, Ying, Mei, Yan, Du, Yuguo et Jin, Zhendong, « Total Synthesis of the Highly Potent Anti-HIV Natural Product Daurichromenic Acid along with Its Two Chromane Derivatives, Rhododaurichromanic Acids A and B », Organic Letters, vol. 5, n^o 23,‎ 2003, p. 4481–4484 (PMID 14602030, DOI 10.1021/ol030109m)

chem.nlm.nih.gov

(en) « Acide orsellinique », sur ChemIDplus, consulté le 17 janvier 2011

sis.nlm.nih.gov

(en) « Acide orsellinique », sur ChemIDplus, consulté le 17 janvier 2011

pnas.org

Volker Schroeckh, Kirstin Scherlach, Hans-Wilhelm Nützmann, Ekaterina Shelest, Wolfgang Schmidt-Heck, Julia Schuemann, Karin Martin, Christian Hertweck, Axel A. Brakhage, « Intimate bacterial-fungal interaction triggers biosynthesis of archetypal polyketides in Aspergillus nidulans », Proceedings of the National Academy of Sciences of the United States of America, vol. 106, n^o 34,‎ 2009, p. 14558–14563 (DOI 10.1073/pnas.0901870106}, lire en ligne)

qmul.ac.uk

chem.qmul.ac.uk

Masse molaire calculée d’après « Atomic weights of the elements 2007 », sur www.chem.qmul.ac.uk.