Bibliografías temáticas / Peribysin

Literatura académica sobre el tema "Peribysin"

Autor: Grafiati
Publicado: 6 de septiembre de 2023

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Artículos de revistas sobre el tema "Peribysin"

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Danishefsky, S., A. Angeles, D. Dorn, C. Kou y M. Moore. "Synthesis of ent-Peribysin E". Synfacts 2007, n.º 7 (julio de 2007): 0678. http://dx.doi.org/10.1055/s-2007-968601.

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Angeles, Angie R., Stephen P. Waters y Samuel J. Danishefsky. "Total Syntheses of (+)- and (−)-Peribysin E". Journal of the American Chemical Society 130, n.º 41 (15 de octubre de 2008): 13765–70. http://dx.doi.org/10.1021/ja8048207.

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Lee, Hung-Yi y Chin-Kang Sha. "Stereoselective Total Synthesis of (±)-Peribysin E". Journal of Organic Chemistry 77, n.º 1 (30 de noviembre de 2011): 598–605. http://dx.doi.org/10.1021/jo2021604.

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Kalmode, Hanuman P., Kishor L. Handore, Raveena Rajput, Samir R. Shaikh, Rajesh G. Gonnade, Kiran A. Kulkarni y D. Srinivasa Reddy. "Total Synthesis and Biological Evaluation of Cell Adhesion Inhibitors Peribysin A and B: Structural Revision of Peribysin B". Organic Letters 20, n.º 22 (26 de octubre de 2018): 7003–6. http://dx.doi.org/10.1021/acs.orglett.8b02838.

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Inose, Kota, Kazuaki Tanaka, Takeshi Yamada, Hiroyuki Koshino y Masaru Hashimoto. "Isolation of Peribysins O, P, and Q from Periconia macrospinosa KT3863 and Configurational Reinvestigation of Peribysin E Diacetate from Periconia byssoides OUPS-N133". Journal of Natural Products 82, n.º 4 (15 de febrero de 2019): 911–18. http://dx.doi.org/10.1021/acs.jnatprod.8b01001.

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Athawale, Paresh R., Hanuman P. Kalmode, Zenia Motiwala, Kiran A. Kulkarni y D. Srinivasa Reddy. "Overturning the Peribysin Family Natural Products Isolated from Periconia byssoides OUPS-N133: Synthesis and Stereochemical Revision of Peribysins A, B, C, F, and G". Organic Letters 22, n.º 8 (7 de abril de 2020): 3104–9. http://dx.doi.org/10.1021/acs.orglett.0c00857.

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Handore, Kishor L. y D. Srinivasa Reddy. "A Diverted Total Syntheses of Potent Cell Adhesion Inhibitor Peribysin E Analogues". Organic Letters 15, n.º 8 (4 de abril de 2013): 1894–97. http://dx.doi.org/10.1021/ol400555m.

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8

Angeles, Angie R, David C Dorn, Cynthia A Kou, Malcolm A S. Moore y Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration". Angewandte Chemie 119, n.º 9 (19 de febrero de 2007): 1473–76. http://dx.doi.org/10.1002/ange.200604308.

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Angeles, Angie R, David C Dorn, Cynthia A Kou, Malcolm A S. Moore y Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration". Angewandte Chemie International Edition 46, n.º 9 (19 de febrero de 2007): 1451–54. http://dx.doi.org/10.1002/anie.200604308.

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Azhari, Azmi y Unang Supratman. "The Chemistry and Pharmacology of Fungal Genus Periconia: A Review". Scientia Pharmaceutica 89, n.º 3 (29 de julio de 2021): 34. http://dx.doi.org/10.3390/scipharm89030034.

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Periconia is filamentous fungi belonging to the Periconiaceae family, and over the last 50 years, the genus has shown interest in natural product exploration for pharmacological purposes. Therefore, this study aims to analyze the different species of Periconia containing natural products such as terpenoids, polyketides, cytochalasan, macrosphelides, cyclopentenes, aromatic compounds, and carbohydrates carbasugar derivates. The isolated compound of this kind, which was reported in 1969, consisted of polyketide derivatives and their structures and was determined by chemical reaction and spectroscopic methods. After some years, 77 compounds isolated from endophytic fungus Periconia were associated with eight plant species, 28 compounds from sea hare Aplysia kurodai, and ten from endolichenic fungi Parmelia sp. The potent pharmacological agents from this genus are periconicin A, which acts as an antimicrobial, pericochlorosin B as an anti-human immunodeficiency virus (HIV), peribysin D, and pericosine A as cytotoxic agents, and periconianone A as an anti-inflammatory agent. Furthermore, information about taxol and piperine from Periconia producing species was also provided. Therefore, this study supports discovering new drugs produced by the Periconia species and compares them for future drug development.
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Tesis sobre el tema "Peribysin"

1

李弘毅. "天然物 Ottelione A之合成研究與 Peribysin E 之全合成". Thesis, 2011. http://ndltd.ncl.edu.tw/handle/06219279668574798551.

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Capítulos de libros sobre el tema "Peribysin"

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Taber, Douglass F. "Diels-Alder Cycloaddition: (+)-Armillarivin (Banwell), Gelsemiol (Gademann), (+)-Frullanolide (Liao), Myceliothermophin A (Uchiro), Peribysin E (Reddy), Caribenol A (Li/Yang)". En Organic Synthesis. Oxford University Press, 2015. http://dx.doi.org/10.1093/oso/9780190200794.003.0081.

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Martin G. Banwell of the Australian National University prepared (Org. Lett. 2013, 15, 1934) the enantiomerically pure diol 1 by fermentation of the aromatic precursor. Diels-Alder addition of cyclopentenone 2 proceeded well at elevated pressure to give 3, the precursor to (+)-armillarivin 4. Karl Gademann of the University of Basel found (Chem. Eur. J. 2013, 19, 2589) that the Diels-Alder addition of 6 to 5 proceeded best without solvent and with Cu catalysis to give 7. Reduction under free radical conditions led to gelsemiol 8. Chun-Chen Liao of the National TsingHua University carried out (Org. Lett. 2013, 15, 1584) the diastereoselective addition of 10 to 9. A later oxy-Cope rearrangement established the octalin skeleton of (+)-frullanolide 12. D. Srinivasa Reddy of CSIR-National Chemical Laboratory devised (Org. Lett. 2013, 15, 1894) a strategy for the construction of the angularly substituted cis-fused aldehyde 15 based on Diels-Alder cycloaddition of 14 to the diene 13. Further transformation led to racemic peribysin-E 16. An effective enantioselective catalyst for dienophiles such as 14 has not yet been developed. Hiromi Uchiro of the Tokyo University of Science prepared (Tetrahedron Lett. 2012, 53, 5167) the bicyclic core of myceliothermophin A 19 by BF3•Et2O-promoted cyclization of the tetraene 17. The single ternary center of 17 mediated the formation of the three new stereogenic centers of 18, including the angular substitution. En route to caribenol A 22, Chuang-Chuang Li and Zhen Yang of the Peking University Shenzen Graduate School assembled (J. Org. Chem. 2013, 78, 5492) the triene 20 from two enantiomerically pure precursors. Inclusion of the radical inhibitor BHT sufficed to suppress competing polymerization, allowing clean cyclization to 21. Methylene blue has also been used (J. Am. Chem. Soc. 1980, 102, 5088) for this purpose.
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