Academic literature on the topic 'Peribysin'

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Journal articles on the topic "Peribysin"

1

Danishefsky, S., A. Angeles, D. Dorn, C. Kou, and M. Moore. "Synthesis of ent-Peribysin E." Synfacts 2007, no. 7 (2007): 0678. http://dx.doi.org/10.1055/s-2007-968601.

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2

Angeles, Angie R., Stephen P. Waters, and Samuel J. Danishefsky. "Total Syntheses of (+)- and (−)-Peribysin E." Journal of the American Chemical Society 130, no. 41 (2008): 13765–70. http://dx.doi.org/10.1021/ja8048207.

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3

Lee, Hung-Yi, and Chin-Kang Sha. "Stereoselective Total Synthesis of (±)-Peribysin E." Journal of Organic Chemistry 77, no. 1 (2011): 598–605. http://dx.doi.org/10.1021/jo2021604.

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4

Kalmode, Hanuman P., Kishor L. Handore, Raveena Rajput, et al. "Total Synthesis and Biological Evaluation of Cell Adhesion Inhibitors Peribysin A and B: Structural Revision of Peribysin B." Organic Letters 20, no. 22 (2018): 7003–6. http://dx.doi.org/10.1021/acs.orglett.8b02838.

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5

Inose, Kota, Kazuaki Tanaka, Takeshi Yamada, Hiroyuki Koshino, and 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, no. 4 (2019): 911–18. http://dx.doi.org/10.1021/acs.jnatprod.8b01001.

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6

Athawale, Paresh R., Hanuman P. Kalmode, Zenia Motiwala, Kiran A. Kulkarni, and 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, no. 8 (2020): 3104–9. http://dx.doi.org/10.1021/acs.orglett.0c00857.

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7

Handore, Kishor L., and D. Srinivasa Reddy. "A Diverted Total Syntheses of Potent Cell Adhesion Inhibitor Peribysin E Analogues." Organic Letters 15, no. 8 (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, and Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration." Angewandte Chemie 119, no. 9 (2007): 1473–76. http://dx.doi.org/10.1002/ange.200604308.

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9

Angeles, Angie R, David C Dorn, Cynthia A Kou, Malcolm A S. Moore, and Samuel J Danishefsky. "Total Synthesis of Peribysin E Necessitates Revision of the Assignment of its Absolute Configuration." Angewandte Chemie International Edition 46, no. 9 (2007): 1451–54. http://dx.doi.org/10.1002/anie.200604308.

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10

Azhari, Azmi, and Unang Supratman. "The Chemistry and Pharmacology of Fungal Genus Periconia: A Review." Scientia Pharmaceutica 89, no. 3 (2021): 34. http://dx.doi.org/10.3390/scipharm89030034.

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Abstract:
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 spectros
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