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Journal articles on the topic 'Viridiofungin A'

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

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1

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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2

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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3

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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4

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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5

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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6

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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7

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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8

Goldup, Stephen M., Christopher J. Pilkington, Andrew J. P. White, Andrew Burton, and Anthony G. M. Barrett. "Correction to “A Simple, Short, and Flexible Synthesis of Viridiofungin Derivatives”." Journal of Organic Chemistry 84, no. 10 (2019): 6546. http://dx.doi.org/10.1021/acs.joc.9b01172.

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9

Ghosh, Arun K., and Jorden Kass. "A Stereoselective Synthesis of (−)-Viridiofungin A Utilizing a TiCl4-Promoted Asymmetric Multicomponent Reaction." Organic Letters 14, no. 2 (2011): 510–12. http://dx.doi.org/10.1021/ol203093g.

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10

Pollex, Annett, Lars Abraham, Jana Müller, and Martin Hiersemann. "Total synthesis of (3S,4S,2′S)- and (3R,4R,2′S)-viridiofungin A triester." Tetrahedron Letters 45, no. 37 (2004): 6915–18. http://dx.doi.org/10.1016/j.tetlet.2004.07.086.

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11

El-Hasan, Abbas, Frank Walker, Jochen Schöne, and Heinrich Buchenauer. "Detection of viridiofungin A and other antifungal metabolites excreted by Trichoderma harzianum active against different plant pathogens." European Journal of Plant Pathology 124, no. 3 (2009): 457–70. http://dx.doi.org/10.1007/s10658-009-9433-3.

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12

Pollex, Annett, Agnès Millet, Jana Müller, Martin Hiersemann, and Lars Abraham. "Ester Dienolate [2,3]-Wittig Rearrangement in Natural Product Synthesis: Diastereoselective Total Synthesis of the Triester of Viridiofungin A, A2, and A4." Journal of Organic Chemistry 70, no. 14 (2005): 5579–91. http://dx.doi.org/10.1021/jo0505270.

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13

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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14

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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15

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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16

Harris, Guy H., E. Tracy Turner Jones, Maria S. Meinz, et al. "Isolation and structure elucidation of viridiofungins A, B and C." Tetrahedron Letters 34, no. 33 (1993): 5235–38. http://dx.doi.org/10.1016/s0040-4039(00)73961-x.

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17

Kumagai, Naoya, and Masakatsu Shibasaki. "Synthetic studies of viridiofungins, broad-spectrum antifungal agents and serine palmitoyl transferase inhibitors." Journal of Antibiotics 71, no. 1 (2017): 53–59. http://dx.doi.org/10.1038/ja.2017.110.

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18

Morokuma, Kenji, Keisuke Takahashi, Jun Ishihara, and Susumi Hatakeyama. "Total Synthesis of Viridiofungin A." ChemInform 36, no. 38 (2005). http://dx.doi.org/10.1002/chin.200538212.

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