Natuurproduct (scheikunde) (Dutch Wikipedia)

Analysis of information sources in references of the Wikipedia article "Natuurproduct (scheikunde)" in Dutch language version.

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10nih.gov

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acs.org

pubs.acs.org

(en) M.S. Butler (2004) – The Role of Natural Product Chemistry in Drug Discovery, J. Nat. Prod., 67 (12), pp. 2141-2153
(en) B.R. O'Keefe (2001) – Biologically Active Proteins from Natural Product Extracts, J. Nat. Prod., 64 (10), pp. 1373-1381
(en) R.B. Woodward & W.E. Doering (1944) - The Total Synthesis of Quinine, J. Am. Chem. Soc., 66 (5), pp. 849-849
(en) R.B. Woodward, M.P. Cava, W.D. Ollis, A. Hunger, H.U. Daeniker & K. Schenker (1954) – The Total Synthesis of Strychnine, J. Am. Chem. Soc., 76 (18), pp. 4749-4751
(en) E.J. Corey, M.C. Kang, M.C. Desai, A.K. Ghosh & I.N. Houpis (1988) – Total synthesis of (±)-ginkgolide B, J. Am. Chem. Soc., 110 (2), pp. 649-651
(en) G. Zhou & E.J. Corey (2005) – Short, Enantioselective Total Synthesis of Aflatoxin B₂ Using an Asymmetric [3+2]-Cycloaddition Step, J. Am. Chem. Soc., 127 (34), pp. 11958-11959
(en) M.-Z. Wang, H. Xu, Q. Feng, L.-Z. Wang, S.-H. Wang & Z.-M. Li (2009) – Design, Synthesis, and Fungicidal Activity of Novel Analogues of Pyrrolnitrin, J. Agric. Food Chem., 57 (17), pp. 7912-7918
(en) G. Büchi, R.E. Erickson & N. Wakabayashi (1961) – Terpenes. XVI. Constitution of Patchouli Alcohol and Absolute Configuration of Cedrene, J. Am. Chem. Soc., 83 (4), pp. 927-938
(en) G. Büchi & W.D. Macleod (1962) – Synthesis of Patchouli Alcohol, J. Am. Chem. Soc., 84 (16), pp. 3205-3206

acs.org

(en) The Chemical Revolution of Antoine-Laurent Lavoisier, American Chemical Society, 1999

annualreviews.org

(en) K.M. Herrmann & L.M. Weaver (1999) – The Shikimate Pathway, Annual Review of Plant Physiology and Plant Molecular Biology, 50, pp. 473-503
(en) T.S. Dhadialla, G.R. Carlson & D.P. Le (1998) – New insecticides with ecdysteroidal and juvenile hormone activity, Annual Review of Entomology, 43, pp. 545-569
(en) J.E. Casida, D.W. Gammon, A.H. Glickman & L.J. Lawrence (1983) – Mechanisms of Selective Action of Pyrethroid Insecticides, Annual Review of Pharmacology and Toxicology, 23, pp. 413-438

archive.org

(de) A. Kossel (1891) – Ueber die chemische Zusammensetzung der Zelle, Archiv für Physiologie, pp. 181-186

books.google.com

(en) Cutler S, Cutler HG (2000). Biologically Active Natural Products: Pharmaceuticals. CRC Press, p. 5. ISBN 978-0-8493-1887-0.

cabdirect.org

(en) G.E. Pratt, R.C. Jennings, A.F. Hamnett & G.T. Brooks (1980) – Lethal metabolism of precocene-I to a reactive epoxide by locust corpora allata, Nature, 284 (5754), pp. 320-323

catbull.com

(en) R.J.P. Cannell (1998) – How to Approach the Isolation of a Natural Product?, Methods in Biotechnology, 4, pp. 1-51

chemheritage.org

(en) Justus von Liebig and Friedrich Wöhler, Chemical Heritage Foundation (CHF)

d-nb.info

(en) C.-D. Pham (2014) – New cytotoxic marine natural products from marine invertebrates, doctoraatsthesis, Heinrich-Heine-Universität Düsseldorf, p. 12

degruyter.com

(en) R.B. Woodward (1973) – The total synthesis of vitamin B₁₂, Pure Appl. Chem., 33 (1), pp. 145-178

eurekaselect.com

(en) J.M. Sabatier (2011) – Animal venoms: from deadly arsenals (toxins) to therapeutic drug candidates, Inflamm. Allergy Drug Targets, 10 (5), p. 312

fasebj.org

(en) C.G. Smith & J.R. Vane (2003) – The Discovery of Captopril, The FASEB Journal, 17 (8), pp. 788-789

mdpi.com

(en) D.A. Dias, S. Urban & U. Roessner (2012) – A Historical Overview of Natural Products in Drug Discovery, Metabolites, 2 (2), pp. 303-336

nature.com

(en) All natural, Nature Chemical Biology, 3 (7), p. 351 (2007)
(en) K.C. Nicolaou, Z. Yang, J.J. Liu, H. Ueno, P.G. Nantermet, R.K. Guy, C.F. Claiborne, J. Renaud, E.A. Couladouros, K. Paulvannan & E.J. Sorensen (1994) – Total synthesis of taxol, Nature, 367 (6464), pp. 630-634
(en) K.C. Nicolaou, Z. Yang, J.J. Liu, H. Ueno, P.G. Nantermet, R.K. Guy, C.F. Claiborne, J. Renaud, et al. (1994) – Total synthesis of taxol, Nature, 367 (6464), pp. 630-634
(en) A. Rowan (2005) – Lead Optimization: Improving natural strength, Nature Reviews Drug Discovery, 4, p. 1041

nih.gov

ncbi.nlm.nih.gov

(en) S.L. Robinette, R. Brüschweiler, F.C. Schroeder & A.S. Edison (2012) – NMR in metabolomics and natural products research: two sides of the same coin, Acc. Chem. Res., 45 (2), pp. 288-297
(en) R. Montaser & H. Luesch (2011) – Marine natural products: a new wave of drugs?, Future Med Chem., 3 (12), pp. 1475-1489
(en) J.G. Napolitano, A.H. Daranas, M. Norte & J.J. Fernández (2009) – Marine macrolides, a promising source of antitumor compounds, Anticancer Agents Med. Chem., 9 (2), pp. 122-137
(en) M.G. Bock, R.M. DiPardo, K.E. Rittle, B.E. Evans, R.M. Freidinger, D.F. Veber, R.S. Chang, T.B. Chen, M.E. Keegan & V.J. Lotti (1986) – Cholecystokinin antagonists. Synthesis of asperlicin analogues with improved potency and water solubility, J. Med. Chem., 29(10), pp. 1941-1945
(en) M.A. Koch, A. Schuffenhauer, M. Scheck, S. Wetzel, M. Casaulta, A. Odermatt, P. Ertl & H. Waldmann (2005) – Charting biologically relevant chemical space: A structural classification of natural products (SCONP), Proc. Natl. Acad. Sci. USA, 102 (48), pp. 17272-17277
(en) F.E. Koehn & G.T. Carter (2005) – The evolving role of natural products in drug discovery, Nat. Rev. Drug. Discov., 4 (3), pp. 206-220
(en) K.W. Cheng, C.C. Wong, M. Wang, Q.F. He & F. Chen (2010) – Identification and characterization of molecular targets of natural products by mass spectrometry, Mass Spectrom. Rev., 29 (1), pp. 126-155
(en) R.C. Breton & W.F. Reynolds (2013) – Using NMR to identify and characterize natural products, Nat. Prod. Rep., 30 (4), pp. 501-524
(en) A.M. Lourenco, L.M. Ferreira & P.S. Branco (2012) – Molecules of natural origin, semi-synthesis and synthesis with anti-inflammatory and anticancer utilities, Curr. Pharm. Des., 18 (26), pp. 3979-4046
(en) B.B. Petrovska (2012) – Historical review of medicinal plants' usage, Pharmacogn. Rev., 6 (11), pp. 1-5

nobelprize.org

(en) B.G. Malmström & B. Andersson (2001) – The Nobel Prize in Chemistry: The Development of Modern Chemistry

opiates.net

(en) A brief history of opium, opiates.net

oxfordjournals.org

aob.oxfordjournals.org

(en) P.W. Brian (1949) – Studies on the Biological Activity of Griseofulvin, Ann. Bot., 13 (1), pp. 59-77

plosone.org

(en) J. Gu, Y. Gui, L. Chen, G. Yuan, H.-Z. Lu & X. Xu (2013) – Use of Natural Products as Chemical Library for Drug Discovery and Network Pharmacology, PLoS ONE, 8(4)

rsc.org

pubs.rsc.org

(en) R.N. Strange (2007) – Phytotoxins produced by microbial plant pathogens, Nat. Prod. Rep., 24 (1), pp. 127-144
(en) A.T. Dossey (2010) – Insects and their chemical weaponry: new potential for drug discovery, Nat. Prod. Rep., 27 (12), pp. 1737-1757
(en) F. Bucar, A. Wubea & M. Schmid (2013) – Natural product isolation – how to get from biological material to pure compounds, Nat. Prod. Rep., 30, pp. 525-545

sciencedirect.com

(en) R.A. Maplestone, M.J. Stone & D.H. Williams (1992) – The evolutionary role of secondary metabolites - a review, Gene, 115 (1–2), pp. 151-157
(en) S.M.K. Rates (2001) – Plants as source of drugs, Toxicon, 39 (5), pp. 603-613
(en) W. Kraus, M. Bokel, A. Klenk & H. Pöhn (1985) – The structure of azadirachtin and 22,23-dihydro-23β-methoxyazadirachtin, Tetrahedron Letters, 26 (52), pp. 6435-6438

sciencemag.org

(en) A. Eschenmoser & C.E. Wintner (1977) – Natural Product Synthesis and Vitamin B₁₂, Science, 196 (4297), pp. 1410-1420

springer.com

link.springer.com

(en) A.L. Demain & A. Fang (2000) – The natural functions of secondary metabolites, Adv. Biochem. Eng. Biotechnol., 69, pp. 1-39
(de) A. Eschenmoser (1974) – Organische Naturstoffsynthese heute: Vitamin B₁₂ als Beispiel, Naturwissenschaften, 61 (12), pp. 513-525

tandfonline.com

(en) J. Khazirb, B.A. Mirc, S.A. Mird & D. Cowanc (2013) – Natural products as lead compounds in drug discovery, Journal of Asian Natural Products Research, 15 (7), pp. 764-788

web.archive.org

(en) K.K. Dholwani, A.K. Saluja, A.R. Gupta & D.R. Shah (2008) – A review on plant-derived natural products and their analogs with anti-tumor activity, Indian J. Pharmacol., 40 (2), pp. 49-58
(en) H. Tesso (2005) – Isolation and Structure Elucidation of Natural Products from Plants, doctoraatsthesis, Universiteit van Hamburg, pp. 16-27

wiley.com

onlinelibrary.wiley.com

(de) F. Wöhler (1828) - Ueber künstliche Bildung des Harnstoffs, Annalen der Physik und Chemie, 88 (2), pp. 253-256
(de) J. von Liebig (1838) – Ueber Laurent's Theorie der organischen Verbindungen, Ann. Pharm., 25 (1), pp. 1-31
(de) A. Kekulé (1858) – Ueber die Constitution und die Metamorphosen der chemischen Verbindungen und über die chemische Natur des Kohlenstoffs, Annalen der Chemie und Pharmacie, 106 (2), pp. 129-159
(en) D.J. Kliebenstein (2004) – Secondary metabolites and plant/environment interactions: a view through Arabidopsis thaliana tinged glasses, Plant, Cell and Environment, 27 (6), pp. 675-684
(en) R.D. Firn & C.G. Jones (2000) – The evolution of secondary metabolism - a unifying model, Mol. Microbiol., 37 (5), pp. 989-994
(en) F. Lévesque & P.H. Seeberger (2012) – Continuous-Flow Synthesis of the Anti-Malaria Drug Artemisinin, Angew. Chem. Int. Ed., 51 (7), pp. 1706-1709
(en) C.F. Nising & S. Bräse (2008) – Highlights in Steroid Chemistry: Total Synthesis versus Semisynthesis, Angew. Chem. Int. Ed., 47 (49), pp. 9389-9391
(en) A.J. Mordue, M.S.J. Simmonds, S.V. Ley, W.M. Blaney, W. Mordue, M. Nasiruddin & A.J. Nisbet (1998) – Actions of azadirachtin, a plant allelochemical, against insects, Pesticide Science, 54 (3), pp. 277-284