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Relevant bibliographies by topics / Taiwaniaquinoid

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Journal articles

Academic literature on the topic 'Taiwaniaquinoid'

Author: Grafiati

Published: 20 February 2023

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Journal articles on the topic "Taiwaniaquinoid"

1

Graham, Marlowe, Robert W. Baker, and Christopher S. P. McErlean. "Cationic Polyene Cyclization for Taiwaniaquinoid Construction." European Journal of Organic Chemistry 2017, no. 4 (2017): 908–13. http://dx.doi.org/10.1002/ejoc.201601349.

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2

Guardia, Juan J., Antonio Fernández, José Justicia, et al. "Unprecedented Elimination Reactions of Cyclic Aldols: A New Biosynthetic Pathway toward the Taiwaniaquinoid Skeleton." Molecules 28, no. 4 (2023): 1524. http://dx.doi.org/10.3390/molecules28041524.

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The acid treatment of 6,7-seco-abietane dialdehydes gives, in high yield, the corresponding derivatives with the 4a-methyltetrahydrofluorene skeleton of taiwaniaquinoids. A mechanism involving the elimination of formic acid from the cyclic aldol intermediate is proposed here. This process can be postulated as a new biogenetic pathway from abietane diterpenes to taiwaniaquinoids. Using this novel reaction, the first enantiospecific synthesis of bioactive natural cupresol and taxodal has been obtained.

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3

Meng, Yonggang, Yizhen Liu, Zhigang Lv, et al. "Concise Synthesis of Taiwaniaquinol B and 5-epi-Taiwaniaquinone G." Natural Product Communications 10, no. 12 (2015): 1934578X1501001. http://dx.doi.org/10.1177/1934578x1501001204.

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The natural product taiwaniaquinol B and the unnatural 5- epi-taiwaniaquinone G were synthesized based on a highly efficient tandem acylation–Nazarov cyclization approach to build the tricyclic skeleton.

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4

Kakde, Badrinath N., Pooja Kumari, and Alakesh Bisai. "Total Synthesis of (±)-Taiwaniaquinol F and Related Taiwaniaquinoids." Journal of Organic Chemistry 80, no. 20 (2015): 9889–99. http://dx.doi.org/10.1021/acs.joc.5b01345.

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5

Ramírez-Macías, Inmaculada, Clotilde Marín, Hakima Es-Samti, et al. "Taiwaniaquinoid and abietane quinone derivatives with trypanocidal activity against T. cruzi and Leishmania spp." Parasitology International 61, no. 3 (2012): 405–13. http://dx.doi.org/10.1016/j.parint.2012.02.001.

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6

Kakde, Badrinath N., Pooja Kumari, and Alakesh Bisai. "ChemInform Abstract: Total Synthesis of (.+-.)-Taiwaniaquinol F and Related Taiwaniaquinoids." ChemInform 47, no. 10 (2016): no. http://dx.doi.org/10.1002/chin.201610207.

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7

Alvarez-Manzaneda, Enrique, Rachid Chahboun, Eduardo Cabrera, et al. "An enantiospecific route towards taiwaniaquinoids. First synthesis of (−)-taiwaniaquinone H and (−)-dichroanone." Organic & Biomolecular Chemistry 7, no. 24 (2009): 5146. http://dx.doi.org/10.1039/b916209g.

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8

Majetich, George, and Joel M. Shimkus. "Concise syntheses of (±)-dichroanone, (±)-dichroanal B, (±)-taiwaniaquinol B, and (±)-taiwaniaquinone D." Tetrahedron Letters 50, no. 26 (2009): 3311–13. http://dx.doi.org/10.1016/j.tetlet.2009.02.074.

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9

Alvarez-Manzaneda, Enrique, Rachid Chahboun, Eduardo Cabrera та ін. "A thermal 6π electrocyclization strategy towards taiwaniaquinoids. First enantiospecific synthesis of (−)-taiwaniaquinone G". Chem. Commun., № 5 (2009): 592–94. http://dx.doi.org/10.1039/b816812a.

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10

Thommen, Christophe, Chandan Kumar Jana, Markus Neuburger, and Karl Gademann. "Syntheses of Taiwaniaquinone F and Taiwaniaquinol A via an Unusual Remote C–H Functionalization." Organic Letters 15, no. 6 (2013): 1390–93. http://dx.doi.org/10.1021/ol4003652.

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