Relevant bibliographies by topics / Taraxasteryl Acetate

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Academic literature on the topic 'Taraxasteryl Acetate'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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Journal articles on the topic "Taraxasteryl Acetate"

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Reynolds, William F., Jeffery F. Sawyer, Raúl G. Enriquez, Laura I. Escobar, Marco A. Chavez, and James N. Shoolery. "Total assignment of the 13C spectrum of taraxasteryl acetate by 13C–13C connectivity experiments and determination of the stereochemistry of taraxasterol by X-ray diffraction." Canadian Journal of Chemistry 63, no. 5 (1985): 1048–54. http://dx.doi.org/10.1139/v85-178.

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13C–13C connectivity (INADEQUATE) experiments have been used to reassign the 13C spectrum of taraxasteryl acetate. This shows that there were ten errors in an earlier 13C spectral assignment for this compound. An X-ray diffraction investigation of taraxasterol shows that ring E adopts a slightly distorted boat conformation. It is suggested that severe steric interactions in the chair form force it to adopt this unusual conformation. On the basis of the 1H–1H coupling constants, it is concluded that taraxasteryl acetate adopts a very similar conformation in solution. Crystals of taraxasterol–et
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2

U.K., SOM, K. SIL A., B. HAQUE K., and P. DUTTA C. "Oxidation Products of Taraxasteryl Acetate and Molecular Rearrangement of its Epoxide." Journal of Indian Chemical Society Vol. 65, Aug 1988 (1988): 604–6. https://doi.org/10.5281/zenodo.6348801.

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Department of Chemistry, <em>University </em>College of Science, 92 A. P. C. Road, Calcutta-700 009 <em>Manuscript received 31 March 1987, revised 2 March 2988,accepted 3 June 1988</em> Oxidation Products of Taraxasteryl Acetate and Molecular Rearrangement of its Epoxide.
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U.K., SOM, K. SIL A., E. HAQUE K., P. DUTTA C., and DHARA K.P. "Oxidation Products of Taraxasteryl Acetate and Molecular Rearrancement of its Epoxide." Journal of Indian Chemical Society Vol. 65, Aug 1998 (1988): 602–4. https://doi.org/10.5281/zenodo.6076257.

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Department of Chemistry, University of Kalyani,&nbsp;Kalyani-741 235 Department of Chemistry, <em>University </em>College of Science,&nbsp;92 A. P. C. Road, Calcutta-700 009 <em>Manuscript received 31 March 1987, revised 2 March 2988,&nbsp;accepted 3 June 1988</em> <em>Oxidation Products of Taraxasteryl Acetate and Molecular Rearrancement of its Epoxide&nbsp;</em>
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4

Reynolds, William, and Raul Enriquez. "Concerning the Recently Reassigned13C-NMR Spectrum of Taraxasteryl Acetate." Planta Medica 62, no. 05 (1996): 484. http://dx.doi.org/10.1055/s-2006-957952.

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Iijima, Koji, Hiroaki Kiyohara, Morihisa Tanaka, Tsukasa Matsumoto, Jong-Chol Cyong, and Haruki Yamada. "Preventive Effect of Taraxasteryl Acetate fromInula britannicasubsp.japonicaon Experimental Hepatitisin vivo." Planta Medica 61, no. 01 (1995): 50–53. http://dx.doi.org/10.1055/s-2006-957998.

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6

Khalilova, A. Z., I. A. Litvinov, D. V. Beskrovnyi, et al. "Isolation and Crystal Structure of Taraxasteryl Acetate from Onopordum acanthium." Chemistry of Natural Compounds 40, no. 3 (2004): 254–57. http://dx.doi.org/10.1023/b:conc.0000039135.20844.8e.

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7

Bahadır-Acıkara, Özlem, Serkan Özbilgin, Gülcin Saltan-İşcan, et al. "Phytochemical Analysis of Podospermum and Scorzonera n-Hexane Extracts and the HPLC Quantitation of Triterpenes." Molecules 23, no. 7 (2018): 1813. http://dx.doi.org/10.3390/molecules23071813.

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Previously tested n-hexane extracts of the Scorzonera latifolia showed promising bioactivity in vivo. Because triterpenes could account for this activity, n-hexane extracts were analyzed by HPLC to identify and quantify the triterpenes as the most abundant constituents. Other Scorzonera and Podospermum species, potentially containing triterpenic aglycones, were included in the study. An HPLC method for simultaneous determination of triterpene aglycones was therefore developed for analysis of Podospermum and Scorzonera species. n-Hexane extracts of root and aerial parts of S. latifolia, ten oth
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Pérez-García, F., E. Marín, T. Parella, T. Adzet, and S. Cañigueral. "Activity of taraxasteryl acetate on inflammation and heat shock protein synthesis." Phytomedicine 12, no. 4 (2005): 278–84. http://dx.doi.org/10.1016/j.phymed.2004.03.008.

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9

Wu, Jianhao, Jialin Sun, Meiqi Liu, et al. "Botany, Traditional Use, Phytochemistry, Pharmacology and Quality Control of Taraxaci herba: Comprehensive Review." Pharmaceuticals 17, no. 9 (2024): 1113. http://dx.doi.org/10.3390/ph17091113.

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Taraxaci herba, as a traditional Chinese medicine, is the name of the Taraxacum genus in the Asteraceae family. Documented in the Tang Herbal Medicine (Tang Dynasty, AD 657–659), its medicinal properties cover a wide range of applications such as acute mastitis, lung abscess, conjunctival congestion, sore throat, damp-heat jaundice, and vision improvement. In the Chinese Pharmacopoeia (Edition 2020), more than 40 kinds of China-patented drugs containing Taraxaci herba were recorded. This review explores the evolving scientific understanding of Taraxaci herba, covering facets of ethnopharmacolo
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Kirimer, Neş'e, Zeynep Tunalier, K. Can Başer, and Ipek Cingi. "Antispasmodic and Spasmogenic Effects ofScolymus hispanicusand Taraxasteryl Acetate on Isolated Ileum Preparation." Planta Medica 63, no. 06 (1997): 556–58. http://dx.doi.org/10.1055/s-2006-957765.

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Book chapters on the topic "Taraxasteryl Acetate"

1

Taber, Douglass F. "The Corey Synthesis of (+)-Lupeol." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0086.

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The total synthesis of lupeol was one of the crowning achievements of the Robinson annulation/ reductive alkylation approach to stereocontrolled polycarbocyclic construction developed by Gilbert Stork (J. Am. Chem. Soc. 1971, 93, 4945). It is a measure of the progress of organic synthesis since that time that E. J. Corey of Harvard University could devise (J. Am. Chem. Soc. 2009, 131, 13928) an enantioselective synthesis of (+)-lupeol 3 that could be carried out by a single colleague. The key step in the synthesis was the Lewis acid–mediated cyclization of 1 to 2. The preparation of 1 began wi
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