Academic literature on the topic 'Viridiofungina A'

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Journal articles on the topic "Viridiofungina A"

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Huang, Leeyuan, Russell B. Lingham, Guy H. Harris, et al. "New fungal metabolites as potential antihypercholesterolemics and anticancer agents." Canadian Journal of Botany 73, S1 (1995): 898–906. http://dx.doi.org/10.1139/b95-337.

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Several potent inhibitors of squalence synthetase have been discovered. Zaragozic acid A is produced by several fungi; zaragozic acid B is produced by several strains of Sporormiella intermedia; zaragozic acids C, E, and F are produced by Leptodontidium elatius; zaragozic acids D and D2 are produced by Amauroascus niger. L-731,120 and L-731,128 are minor components and coproduced with zaragozic acids A and B, respectively. Viridiofungins A, B, and C are produced by Trichoderma viride. Viridiofungin A is also produced by an unidentified sterile fungus. Several of the zaragozic acids are also po
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ONISHI, J. C., J. A. MILLIGAN, A. BASILIO, et al. "Antimicrobial Activity of Viridiofungins." Journal of Antibiotics 50, no. 4 (1997): 334–38. http://dx.doi.org/10.7164/antibiotics.50.334.

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Hiersemann, H., A. Pollex, A. Millet, J. Müller, and L. Abraham. "Synthesis of Viridiofungin A." Synfacts 2006, no. 01 (2005): 0011. http://dx.doi.org/10.1055/s-2005-921668.

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Murakata, Masatoshi, and Takuma Ikeda. "Stereoselective synthesis of the viridiofungin analogue NA808 from a chiral tetrahydrofuran-carboxylic acid." Organic & Biomolecular Chemistry 15, no. 31 (2017): 6632–39. http://dx.doi.org/10.1039/c7ob01608e.

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The viridiofungin analogue NA808 was synthesized by the stereoselective Ireland–Claisen rearrangement of dienylmethyl ester, regioselective bromolactonization of β-divinylpropanoic acid and retro-bromolactonization.
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Morokuma, Kenji, Keisuke Takahashi, Jun Ishihara, and Susumi Hatakeyama. "Total synthesis of viridiofungin A." Chemical Communications, no. 17 (2005): 2265. http://dx.doi.org/10.1039/b500660k.

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Esumi, Tomoyuki, Yoshiharu Iwabuchi, Hiroshi Irie, and Susumi Hatakeyama. "Synthesis of viridiofungin A trimethyl ester and determination of the absolute structure of viridiofungin A." Tetrahedron Letters 39, no. 8 (1998): 877–80. http://dx.doi.org/10.1016/s0040-4039(97)10754-7.

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MANDALA, SUZANNE M., ROSEMARY A. THORNTON, BETH R. FROMMER, SARAH DREIKORN, and MYRA B. KURTZ. "Viridiofungins, Novel Inhibitors of Sphingolipid Synthesis." Journal of Antibiotics 50, no. 4 (1997): 339–43. http://dx.doi.org/10.7164/antibiotics.50.339.

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ESUMI, T., Y. IWABUCHI, H. IRIE, and S. HATAKEYAMA. "ChemInform Abstract: Synthesis of Viridiofungin A Trimethyl Ester and Determination of the Absolute Structure of Viridiofungin A." ChemInform 29, no. 19 (2010): no. http://dx.doi.org/10.1002/chin.199819242.

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Atkin, Liselle, Angus Robertson, Jonathan M. White, and Mark A. Rizzacasa. "Total Synthesis of Viridiofungins A and B." Organic Letters 23, no. 9 (2021): 3557–60. http://dx.doi.org/10.1021/acs.orglett.1c00971.

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Goldup, Stephen M., Christopher J. Pilkington, Andrew J. P. White, Andrew Burton, and Anthony G. M. Barrett. "A Simple, Short, and Flexible Synthesis of Viridiofungin Derivatives." Journal of Organic Chemistry 71, no. 16 (2006): 6185–91. http://dx.doi.org/10.1021/jo060931e.

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Dissertations / Theses on the topic "Viridiofungina A"

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Saraiva, NatÃlia Nogueira. "Estudo QuÃmico do Fungo Antagonista Trichoderma harzianum." Universidade Federal do CearÃ, 2009. http://www.teses.ufc.br/tde_busca/arquivo.php?codArquivo=4663.

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FundaÃÃo Cearense de Apoio ao Desenvolvimento Cientifico e TecnolÃgico<br>A investigaÃÃo do potencial quÃmico de Trichoderma harzianum, um fungo antagonista, foi realizada. A composiÃÃo de Ãcidos graxos produzidos pelo fungo cultivado em Czapeck, peptona e caldo de batata, variando a fonte de carbono (glicose e manitol), nesse Ãltimo meio, foi determinada por CG/EM. Foram identificados os seguintes Ãcidos graxos na forma dos seus Ãsters metÃlicos: hexadecanÃico (C16:0), octadecanÃico (C18:0), 9-octadecenÃico (C18:1) e 9,12-octadienÃico (C18:2). Dos extratos orgÃnicos do fungo cultivado em pept
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Goldup, Stephen Michael. "The synthesis of Viridiofungin derivatives." Thesis, Imperial College London, 2005. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.421470.

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Pollex, Annett. "Viridiofungins and xeniolide F: target oriented synthesis using different rearrangement reactions of a common substrate class." Doctoral thesis, Saechsische Landesbibliothek- Staats- und Universitaetsbibliothek Dresden, 2006. http://nbn-resolving.de/urn:nbn:de:swb:14-1160474365794-44380.

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The present dissertation covers the total synthesis of viridiofungin triesters and studies toward the total synthesis of xeniolide F. In both cases, sigmatropic rearrangements of α-allyloxy substituted α,β-unsaturated esters are employed: for the viridiofungin ester synthesis a [2,3]-Wittig rearrangement and for the xeniolide F synthesis a catalytic asymmetric Claisen rearrangement CAC. For both rearrangement reactions the historical development, main characteristic and important variations are discussed. The viridiofungin triester synthesis represents a convergent and highly flexible route to
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Pilkington, Christopher John. "The synthesis and synthetic application of resin- supported TosMIC isonitriles in radical cascade reactions and studies towards the synthesis of the antifungal viridiofungins." Thesis, Imperial College London, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.368701.

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Pollex, Annett [Verfasser]. "Viridiofungins and xeniolide F: target oriented synthesis using different rearrangement reactions of a common substrate class / von Annett Pollex." 2006. http://d-nb.info/98163334X/34.

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Book chapters on the topic "Viridiofungina A"

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Mandala, Suzanne M., and Guy H. Harris. "[35] Isolation and characterization of novel inhibitors of sphingolipid synthesis: Australifungin, viridiofungins, rustmicin, and khafrefungin." In Sphingolipid Metabolism and Cell Signaling Part A. Elsevier, 2000. http://dx.doi.org/10.1016/s0076-6879(00)11094-8.

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