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Relevant bibliographies by topics / Baccatin

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Journal articles

Academic literature on the topic 'Baccatin'

Author: Grafiati

Published: 4 June 2021

Last updated: 7 September 2023

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Journal articles on the topic "Baccatin"

1

Kim, Ki-Hyang, Chan-Su Park, Dong-Eun Park, Sun-A. Im, and Chong-Kil Lee. "Immune adjuvant and antitumor activity of baccatin III, a synthetic precursor of taxol (155.15)." Journal of Immunology 186, no. 1_Supplement (2011): 155.15. http://dx.doi.org/10.4049/jimmunol.186.supp.155.15.

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Abstract Baccatin III (BA-III), a precursor for the synthesis of taxol, is widely considered to be an inactive derivative of taxol. Here we show that baccatin III exerts immune adjuvant activity. When added to cultures of immature dendritic cells (DCs) generated from bone marrow cells with GM-CSF, baccatin III increased the expression of MHC II molecules and the allostimulatory activity of the DC. The immune adjuvant activity of baccatin III was examined in mice injected with a model antigen, OVA, emulsified with Freud’s incomplete adjuvant. Inclusion of baccatin III significantly increased th

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2

Ding, Qi, Dong-Mei Fang, Xiao-Huan Li, and Feng Gao. "Two New Taxane Diterpenoids From Taxus baccata." Natural Product Communications 15, no. 9 (2020): 1934578X2095328. http://dx.doi.org/10.1177/1934578x20953280.

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Two new diterpenoids named 13-oxo-wollifoliane-10,15-olide (1) and 19-acetoxy-7,9,10-deacetyl-baccatin VI (2), along with 14 known taxanes (3-16), were isolated from Taxus baccata. The structures of these compounds were elucidated by 1-dimensional and 2-dimensional nuclear magnetic resonance spectra, high-resolution electrospray ionization-mass spectrometry, and infrared spectroscopy. Structurally, 13-oxo-wollifoliane-10,15-olide (1) is the first taxane diterpenoid possessing an unusual carbonyl group at the C-13 position of the 11(15→1),11(10→9)bis- abeo-taxane structure (5/6/6/6/4 skeleton),

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3

Saicic, R. N., R. Matovic, and Z. Cekovic. "Semisynthesis of Taxol®: An improved procedure for the isolation of 10-deacetylbaccatin III." Journal of the Serbian Chemical Society 64, no. 9 (1999): 497–503. http://dx.doi.org/10.2298/jsc9909497s.

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From the needles of domestic yew, (Taxus baccata), 10-deacetylbaccatin III (10-DAB) can be isolated in quantities of up to 297 mg per kg of fresh needles. Additional quantities of 10-Dcan be obtained from the extract by NaBH4 mediated reductive hydrolysis of baccatin esters. A four-step procedure converts 10-Dinto taxol in 58% overall yield.

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4

Chiaroni, A., D. Guénard, F. Guéritte-Voegelein, et al. "A Baccatin III Derivative." Acta Crystallographica Section C Crystal Structure Communications 51, no. 3 (1995): 465–68. http://dx.doi.org/10.1107/s0108270194007341.

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5

Wang, Li, Ya-jun Li, and Zheng-wei Li. "Towards validating new enzymatic routes for synthetic conversion: 7,10-bis-O-(2,2,2-trichloroethoxycarbonyl)-10-deacetyl baccatin III–ethyl acetate–water (1/1/1)." Acta Crystallographica Section C Structural Chemistry 71, no. 3 (2015): 191–94. http://dx.doi.org/10.1107/s2053229614027399.

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The title compound, C34H38Cl6O14·C4H8O2·H2O, prepared by the reaction of 10-deacetyl baccatin III with 2,2,2-trichloroethyl chloroformate in pyridine, crystallizesviastrong intermolecular hydrogen bonds and noncovalent interactions between 7,10-bis-O-(2,2,2-trichloroethoxycarbonyl)-10-deacetyl baccatin III (7,10-di-Troc-DAB), water and ethyl acetate. A detailed comparison of the molecular conformation with those of related structures is presented.

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6

Shen, Ya-Ching, Kuang-Liang Lo, Chun-Ling Lin та Rupak Chakraborty. "Microbial transformation of baccatin VI and 1β-Hydroxy baccatin I by aspergillus niger". Bioorganic & Medicinal Chemistry Letters 13, № 24 (2003): 4493–96. http://dx.doi.org/10.1016/j.bmcl.2003.08.069.

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7

Dutta, Dinah, Apurba Datta, David Vander Velde, and Gunda Georg. "Oxidation of Baccatin III at C14: A Facile Rearrangement of the Baccatin III Core." Letters in Organic Chemistry 4, no. 3 (2007): 151–54. http://dx.doi.org/10.2174/157017807780737246.

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8

Banik, Bimal K., Miguel Fernandez, and Clarissa Alvarez. "Sodium Bismuthate–Induced Oxidation of Baccatin." Synthetic Communications 35, no. 23 (2005): 3065–67. http://dx.doi.org/10.1080/00397910500278842.

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9

Danishefsky, Samuel J., John J. Masters, Wendy B. Young, et al. "Total Synthesis of Baccatin III and Taxol." Journal of the American Chemical Society 118, no. 12 (1996): 2843–59. http://dx.doi.org/10.1021/ja952692a.

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10

Tatini, Lakshmi Kumar, N. Someswara Rao, Muzaffar Khan, Krishna Sumanth Peraka, and K. V. S. R. Krishna Reddy. "Concomitant Pseudopolymorphs of 10-Deacetyl Baccatin III." AAPS PharmSciTech 14, no. 2 (2013): 558–68. http://dx.doi.org/10.1208/s12249-013-9940-6.

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