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1

Provan, Iain. "Pyrrhon, Pyrrhus and the Possibility of the Past: A Response to David Henige." Journal for the Study of the Old Testament 27, no. 4 (June 2003): 413–38. http://dx.doi.org/10.1177/030908920302700402.

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Zaccaria, Pietro. "The Murderers of Kotys the Thracian." Mnemosyne 72, no. 1 (December 6, 2018): 66–83. http://dx.doi.org/10.1163/1568525x-12342522.

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AbstractIn 360/359 BC, Kotys, king of the Odrysian Thracians, was killed by two brothers of Ainos. Confusion, however, soon arose around their identity. The aim of this article is to reconstruct and analyze the various traditions that spread in Antiquity about their identification. Demosthenes was the first to call the murderers Python and Herakleides of Ainos. His version of the facts was later followed by Philodemos, Plutarchos, and Philostratos. Aristoteles, however, called them Πύρρων (or Πάρρων) and Herakleides of Ainos. Diokles of Magnesia, probably following the same tradition as Aristoteles, confused Pyrrhon of Ainos with Pyrrhon of Elis. Similarly, Demetrios of Magnesia confused Herakleides of Ainos with Herakleides Pontikos. Finally, the figures of Kotys, Herakleides, and Python were perhaps reused by the author of the spurious Letters of Chion of Herakleia and recontextualized as symbols of the conflict between philosophy and tyranny.
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3

Ousager, Asger. "Pyrrhon og Platon - mod den metafysiske realisme." Slagmark - Tidsskrift for idéhistorie, no. 20 (February 3, 2018): 87–101. http://dx.doi.org/10.7146/sl.v0i20.103707.

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Det forholdsvis lidet, der er overleveret om skepticismens antikke historie, er for størstepartens vedkommende skrevet af lægen Sextos Empeirikos omkring 200 e.Kr. Sextos var selv skeptisk filosof og var sandsynligvis leder af sin egen skeptiske skole.
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4

Lévy, Carlos. "Scepticisme et rhétorique, de Pyrrhon à Sextus Empiricus." Comptes-rendus des séances de l année - Académie des inscriptions et belles-lettres 156, no. 3 (2012): 1285–301. http://dx.doi.org/10.3406/crai.2012.93702.

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5

Husson, Suzanne. "Pyrrhon (- 360 / - 275) - Le sage est sans opinion." Les Grands Dossiers des Sciences Humaines N° 43, no. 6 (June 1, 2016): 8. http://dx.doi.org/10.3917/gdsh.043.0008.

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6

Held, Klaus. "Von Pyrrhon zu Husserl. Zur Vorgeschichte der phänomenologischen Epoché." Metodo. International Studies in Phenomenology and Philosophy 1, no. 2 (2013): 233–44. http://dx.doi.org/10.19079/metodo.1.2.233.

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7

Luibhéid, Colm. "Pyrrho - M. Conche: Pyrrhon, ou l'Apparence. (Perspectives Critiques.) Pp. 326. Paris: Presses Universitaires de France, 1994. Paper, FF 172." Classical Review 45, no. 2 (October 1995): 293–95. http://dx.doi.org/10.1017/s0009840x00293839.

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8

Pettersen, Bruno. "O PIRRONISMO E AS PAIXÕES: ENTRE A INDIFERENÇA E A ATARAXIA." Sapere Aude 10, no. 19 (July 14, 2019): 43–60. http://dx.doi.org/10.5752/p.2177-6342.2019v10n19p43-60.

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O objetivo deste artigo é examinar a temática das paixões no interior do Pirronismo antigo, especialmente nas figuras de Pirro e Sexto Empírico. Tal questão é controversa em um debate sobre o ceticismo antigo, em especial, porque essa corrente não pode dispor de uma teoria das paixões, dado que elas nada afirmam sobre o mundo. Entretanto, é possível falar que o cético manifesta sentimentos, ainda que de uma maneira não teórica? Para investigarmos essa nuance, passaremos pela vida de Pirro – conforme descrita por Diógenes Laércio – e pelo Esboços do Pirronismo de Sexto Empírico, em busca de uma reflexão acerca das paixões no interior do ceticismo pirrônico.PALAVRAS-CHAVES: Pirro. Sexto Empírico. Paixões. Ceticismo. Diógenes Laércio. ABSTRACTThe purpose of this paper is to examine the passions within the ancient Pyrrhonism, especially in the figures of Pyrrho and Sextus Empiricus. This question is controversial in a debate about ancient skepticism, especially because the skeptics cannot have a theory of passions, since they claim nothing about the world. However, is it possible to speak that the skeptic expresses feelings, albeit in a non-theoretical way? To examine this question, we will go through the life of Pyrrhus - as described by Diogenes Laertius – and we will examine the Outlines of Scepticism by Sextus Empiricus in search of a reflection on the passions within the Pyrrhonic skepticism.KEY-WORDS: Pyrrho. Sixth Empiricus. Passions. Skepticism. Diogenes Laertius.
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9

Warren, James. "Aristocles' refutations of Pyrrhonism (Eus. PE 14.18.1–10)." Proceedings of the Cambridge Philological Society 46 (2001): 140–64. http://dx.doi.org/10.1017/s0068673500002480.

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It has been generally agreed for some time that the best piece of extant evidence for Pyrrho's thought is contained in a section of Eusebius' Praeparatio evangelica (14.18.1–4 = T53 Decleva Caizzi) where Eusebius cites Aristocles of Messene's πεϱὶ ϕιλοσοϕίας book eight, where Aristocles in turn cites Timon on Pyrrho. But there the agreement stops. The wealth of recent writing on this very short passage provides evidence of its difficulty. Ausland, Bett, Brennan, Brunschwig, and Stopper have all within the last ten years or so offered their own various interpretations of these dozen lines of Greek text.
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10

Warren, James. "Pyrrho." Classical Review 51, no. 2 (October 2001): 293–95. http://dx.doi.org/10.1093/cr/51.2.293.

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11

Perricone, Nicholas. "Pyrrho+." Journal of Cosmetic Dermatology 3, no. 3 (July 2004): 179. http://dx.doi.org/10.1111/j.1473-2130.2004.00133.x.

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12

Abbasov, Namig, and Emil A. Souleimanov. "Putin als Pyrrhos." osteuropa 70, no. 6 (2020): 165. http://dx.doi.org/10.35998/oe-2020-0042.

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13

Zelikson, Denis. "ПИРРОВА ПОБЕДА ГРЕЧЕСКОЙ ДИПЛОМАТИИ." Scientific and Analytical Herald of IE RAS 1, no. 2 (March 1, 2018): 55–59. http://dx.doi.org/10.15211/vestnikieran220189.

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14

yu-suk oh. "Was Pyrrho a sceptic?" Studies in Philosophy East-West ll, no. 70 (December 2013): 237–63. http://dx.doi.org/10.15841/kspew..70.201312.237.

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15

Brennan, Tad. "Pyrrho on the Criterion." Ancient Philosophy 18, no. 2 (1998): 417–34. http://dx.doi.org/10.5840/ancientphil199818239.

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16

Nikitin, Kirill V., and Nonna P. Andryukhova. "Synthesis of 5-alkyl- and 5-aryl-1,5-dihydro-2H-pyrrol-2-ones via coupling of 5-chloro-1,5-dihydro-2H-pyrrol-2-ones with organometallic compounds." Canadian Journal of Chemistry 78, no. 10 (October 1, 2000): 1285–88. http://dx.doi.org/10.1139/v00-127.

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5-Chloro-1,5-dihydro-2H-pyrrol-2-ones are easily alkylated at the 5-position by organomagnesium or organozinc compounds and diethyl sodiomalonate leading to corresponding 5-alkyl-1,5-dihydro-2H-pyrrol-2-ones in high yields.Key words: organometallic compounds, alkylation, 1,5-dihydro-2H-pyrrol-2-one.
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17

Frenzel, Andrea, Regine Herbst-Irmer, Uwe Klingebiel, Mathias Noltemeyer, and Martina Schäfer. "Indolyl- und Pyrrolylsilane – Synthese und Kristallstruktur / Indolyl- and Pyrrolylsilanes – Syntheses and Crystal Structures." Zeitschrift für Naturforschung B 50, no. 11 (November 1, 1995): 1658–64. http://dx.doi.org/10.1515/znb-1995-1112.

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Lithium indolide and lithium pyrrolide react with fluoro- and chlorosilanes with formation of mono- and bis(indol-1-yl)- and -(pyrrol-1-yl)silanes, tris- and tetrakis(pyrrol-1-yl)silanes as well as of silanes substituted with different heteroaromatic systems. The crystal structures of the lithium indolide and the tetrakis(pyrrol-1-yl)silane have been determined and are discussed.
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18

Lai, W. "Pyrrhic victories." Canadian Medical Association Journal 178, no. 4 (February 12, 2008): 388. http://dx.doi.org/10.1503/cmaj.080037.

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19

Graham, Hannah. "Pyrrhic liturgy." Crime, Media, Culture: An International Journal 14, no. 2 (January 9, 2018): 343–44. http://dx.doi.org/10.1177/1741659017751224.

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20

Miller, James. "Pyrrhonic Liberalism." Political Theory 28, no. 6 (December 2000): 810–21. http://dx.doi.org/10.1177/0090591700028006005.

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21

Bentley, Roger. "Pyrrhic Victories." British Journal of Occupational Therapy 53, no. 1 (January 1990): 1. http://dx.doi.org/10.1177/030802269005300101.

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22

Cullity, Garrett. "PYRRHIC PYRRHONISM." Philosophical Quarterly 58, no. 233 (October 2008): 720–31. http://dx.doi.org/10.1111/j.1467-9213.2008.527.x.

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23

Wu, Ya-Tong, Rui Zhang, Xiao-Yong Duan, Hai-Fei Yu, Bo-Yu Sun, and Jing Qi. "Access to dihydropyrano[3,2-b]pyrrol-5-ones skeletons by N-heterocyclic carbene-catalyzed [3+3] annulations." Chemical Communications 56, no. 68 (2020): 9854–57. http://dx.doi.org/10.1039/d0cc04661b.

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24

Böttger, Matthias, Björn Wiegmann, Steffen Schaumburg, Peter G. Jones, Wolfgang Kowalsky, and Hans-Hermann Johannes. "Synthesis of new pyrrole–pyridine-based ligands using an in situ Suzuki coupling method." Beilstein Journal of Organic Chemistry 8 (July 9, 2012): 1037–47. http://dx.doi.org/10.3762/bjoc.8.116.

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The compounds 6-(pyrrol-2-yl)-2,2‘-bipyridine, 2-(pyrrol-2-yl)-1,10-phenanthroline and 2-(2-(N-methylbenz[d,e]imidazole)-6-(pyrrol-2-yl)-pyridine were synthesized by using an in situ generated boronic acid for the Suzuki coupling. Crystals of the products could be grown and exhibited interesting structures by X-ray analysis, one of them showing a chain-like network with the adjacent molecules linked to each other via intermolecular N–H…N hydrogen bonds.
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25

Ziemińska, Renata. "Was Pyrrho the Founder of Skepticism?" Polish Journal of Philosophy 5, no. 1 (2011): 149–56. http://dx.doi.org/10.5840/pjphil2011518.

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26

Castagnoli, Luca. "Pyrrho, his Antecedents, and his Legacy." Ancient Philosophy 22, no. 2 (2002): 443–57. http://dx.doi.org/10.5840/ancientphil200222237.

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27

Dimech, Dominic K. "Hume is the Enemy of Pyrrho." Philosophy 96, no. 4 (May 28, 2021): 651–74. http://dx.doi.org/10.1017/s0031819121000188.

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AbstractI offer reasons against reading Hume as a Pyrrhonian sceptic. I argue that Hume's scepticism is motivated differently, that his sceptical strategies are not analogous to Pyrrhonism's, and that it is profitable to read Hume as a critic of Pyrrhonism. I hold that the most informative point of comparison between Hume and Sextus Empiricus is a point of difference, namely, their stands on the connection between suspension of judgement (epochê) and tranquillity (ataraxia). For Sextus, tranquillity flows naturally from suspending judgement on all opinions. Hume, by contrast, consistently treats radical suspension of judgement as resulting in despair and social detachment. I take a firmer stance than past commentators on this issue by affirming that Hume and Sextus do not merely disagree on this issue, but that Hume's view is more plausible. Reading Hume's sceptical crisis, I propose, reveals an insightful criticism of Pyrrhonism, one that sheds light on human nature's response to radical doubt.
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28

Sathiyaraj, Ethiraj, Govindasamy Gurumoorthy, and Subbiah Thirumaran. "Nickel(ii) dithiocarbamate complexes containing the pyrrole moiety for sensing anions and synthesis of nickel sulfide and nickel oxide nanoparticles." New Journal of Chemistry 39, no. 7 (2015): 5336–49. http://dx.doi.org/10.1039/c4nj02250e.

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Rare anagostic interaction is observed in (N-(pyrrol-2-ylmethyl)-N-furfuryldithiocarbamato-S,S′)(thiocyanato-N)(triphenylphosphine)nickel(ii). Bis(N-(pyrrol-2-ylmethyl)-N-furfuryldithiocarbamato-S,S′)nickel(ii) is used for the preparation of spherical nickel sulfide and nickel oxide nanoparticles.
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29

Harrison, Trevor. "STEPPING STONE OR PYRRHIC VICTORY? REFORM AND THE REFERENDUM." Constitutional Forum / Forum constitutionnel 4, no. 1 - 4 (October 11, 2011): 1993. http://dx.doi.org/10.21991/c9md46.

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30

Karsenti, Tiphaine. "« Pyrrhe sera toujours pire ». Enjeux idéologiques et esthétiques du traitement de la mort de Pyrrhus dans la tragédie des années 1590." Albineana, Cahiers d'Aubigné 20, no. 1 (2008): 117–32. http://dx.doi.org/10.3406/albin.2008.1111.

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31

Sweeting, Stephen G., Charlie L. Hall, Jason Potticary, Natalie E. Pridmore, Stephen D. Warren, Matthew E. Cremeens, Gemma D. D'Ambruoso, Masaomi Matsumoto, and Simon R. Hall. "The solubility and stability of heterocyclic chalcones compared with trans-chalcone." Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials 76, no. 1 (February 1, 2020): 13–17. http://dx.doi.org/10.1107/s2052520619015907.

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Heterocyclic chalcones are a recently explored subgroup of chalcones that have sparked interest due to their significant antibacterial and antifungal capabilities. Herein, the structure and solubility of two such compounds, (E)-1-(1H-pyrrol-2-yl)-3-(thiophen-2-yl)prop-2-en-1-one and (E)-3-phenyl-1-(1H-pyrrol-2-yl)prop-2-en-1-one, are assessed. Single crystals of (E)-1-(1H-pyrrol-2-yl)-3-(thiophen-2-yl)prop-2-en-1-one were grown, allowing structural comparisons between the heterocyclic chalcones and (2E)-1,3-diphenylprop-2-en-1-one, trivially known as trans-chalcone. The two heterocyclic chalcones were found to be less soluble in all solvents tested and to have higher melting points than trans-chalcone, probably due to their stronger intermolecular interactions arising from the functionalized rings. Interestingly, however, it was found that the addition of the thiophene ring in (E)-1-(1H-pyrrol-2-yl)-3-(thiophen-2-yl)prop-2-en-1-one increased both the melting point and solubility of the sample compared with (E)-3-phenyl-1-(1H-pyrrol-2-yl)prop-2-en-1-one. This observation may be key for the future crystal engineering of heterocyclic chalcones for pharmaceutical applications.
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32

Bach, A., L. Beyer, T. Gelbrich, K. H. Hallmeier, C. Hennig, M. Möbius, R. Richter, R. Szargan, V. Fernandez, and J. Losada. "Metallkomplexe von N-(Pyrrol-l-yl)salicylaldiminen und deren Strukturbestimmung mittels Röntgendiffraktometrie und Röntgenabsorptionsspektroskopie (XANES) / Metal Chelates of N -(Pyrrol-l-yl)salicylaldim ines and their Structure D eterm ination by X-Ray Structure Analysis and X -R ay Absorption Spectroscopy (XANES)." Zeitschrift für Naturforschung B 51, no. 6 (June 1, 1996): 757–64. http://dx.doi.org/10.1515/znb-1996-0601.

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Abstract A series of three N-(pyrrol-l-yl)salicylaldim ines 1-3 has been prepared an d characterized. Their metal chelate complexes with Cu, Ni and Co are described. The molecular structures of bis[N-(pyrrol-l-yl)salicylaldim inato]copper(lI) la, bis{N-[3-(pyrrol-l-yl)propyl]- salicylaldiminato}nickel(II) 2b and tris{N-[3-(pyrrol-l-yl)propyl]salicylaldiminato}cobalt(III) 2d were determined by X-ray structure analysis. The chelates with tetracoordinated copper and nickel show a square planar coordination with the characteristic trans configuration. The chelate with hexacoordinated cobalt has a meridional coordination sphere. The complexes have also been investigated by X-ray absorption spectroscopy (X̲-ray A̲bsorption N̲ear E̲dge S̲tructure, XANES) at the K edges of the 3d metals. Analyzing the relative intensities of the Is → 3d prepeak and the K edges of the line shape, it was possible to distinguish between planar, tetrahedral and octahedral coordination of the chelates
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33

Sha, Qiang, Hadi Arman, and Michael P. Doyle. "Asymmetric synthesis of 1H-pyrrol-3(2H)-ones from 2,3-diketoesters by combination of aldol condensation with benzilic acid rearrangement." Chemical Communications 52, no. 1 (2016): 108–11. http://dx.doi.org/10.1039/c5cc07780j.

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A highly efficient two-step asymmetric synthesis of 1H-pyrrol-3(2H)-one derivatives from conveniently accessed 2,3-diketoesters. Aldol products are obtained with up to 89/11 d.r. and 99% ee. Benzilic acid rearrangement produces 1H-pyrrol-3(2H)-ones in good yields without loss of enantioselectivity.
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34

Svavarsson, Svavar Hrafn. "Pyrrho’s dogmatic nature." Classical Quarterly 52, no. 1 (July 2002): 248–56. http://dx.doi.org/10.1093/cq/52.1.248.

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35

Larkin, John. "A pyrrhic valedictory?" Scottish Medical Journal 63, no. 4 (November 2018): 103. http://dx.doi.org/10.1177/0036933018811242.

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36

Wendover, W. Edward. "Detroit's Pyrrhic Lesson." Newspaper Research Journal 18, no. 1-2 (January 1997): 32. http://dx.doi.org/10.1177/073953299701800104.

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37

Naquin, Paul Jude. "Theism's Pyrrhic Victory." Southern Journal of Philosophy 40, no. 4 (December 2002): 557–71. http://dx.doi.org/10.1111/j.2041-6962.2002.tb01916.x.

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38

Doering, Paula F. "A Pyrrhic Catch." Science News 147, no. 21 (May 27, 1995): 323. http://dx.doi.org/10.2307/3978854.

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39

Reucroft, P. J., H. Scott, and F. L. Serafin. "Photoconducting pyrrone polymers." Journal of Polymer Science Part C: Polymer Symposia 30, no. 1 (March 7, 2007): 261–69. http://dx.doi.org/10.1002/polc.5070300129.

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40

Stauss, Bernd. "A Pyrrhic victory." Managing Service Quality: An International Journal 15, no. 3 (June 2005): 219–29. http://dx.doi.org/10.1108/09604520510597782.

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Quiroga, Diego, Lili Dahiana Becerra, and Ericsson Coy-Barrera. "Solvent Free Three-Component Synthesis of 2,4,5-trisubstituted-1H-pyrrol-3-ol-type Compounds from L-tryptophan: DFT-B3LYP Calculations for the Reaction Mechanism and 3H-pyrrol-3-one↔1H-pyrrol-3-ol Tautomeric Equilibrium." Molecules 25, no. 19 (September 25, 2020): 4402. http://dx.doi.org/10.3390/molecules25194402.

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In this paper, we describe the solvent-free three-component synthesis of 2,4,5-trisubstituted-1H-pyrrol-3-ol-type compounds from L-tryptophan. The first step of the synthetic methodology involved the esterification of L-tryptophan in excellent yields (93–98%). Equimolar mixtures of alkyl 2-aminoesters, 1,3-dicarbonyl compounds, and potassium hydroxide (0.1 eq.) were heated under solvent-free conditions. The title compounds were obtained in moderate to good yields (45%–81%). Density functional theory using “Becke, 3-parameter, Lee–Yang–Parr” correlational functional (DFT-B3LYP) calculations were performed to understand the molecular stability of the synthesized compounds and the tautomeric equilibrium from 3H-pyrrol-3-one type intermediates to 1H-pyrrol-3-ol type aromatized rings.
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Rees, B. J., and J. L. Ye. "Pyrrhoglossum and the small-spored species of Gymnopilus (Cortinariaceae) in eastern Australia." Australian Systematic Botany 12, no. 2 (1999): 255. http://dx.doi.org/10.1071/sb97051.

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Three new species of Gymnopilus subgenusGymnopilus section Microspori aredescribed from eastern Australia. These areGymnopilus marginatus,Gymnopilus patriae andGymnopilus parvisporus. Because of their frequently excentrically stipitate habit and small spore size, the species are comparedwith Pyrrhoglossum pyrrhum (Berk. & M.A.Curtis)Singer, the type species of the genus Pyrrhoglossum,whose presence is also recorded from Australia for the first time. Pigment content of all four species has been examined by thin layer chromatography.Styrylpyrone pigments bis-noryangonin and hispidin were detected in only two of the three Gymnopilus species.Although yellow pigment can be extracted fromPyrrhoglossum pyrrhum, it does not containbis-noryangonin or hispidin.
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43

Wang, Yunlong, Zongyang Li, Haiying Zhao, and Zhenhua Zhang. "Rhodium-Catalyzed Double Isocyanide Insertion via a Vinylcarbodiimide Intermediate for the Synthesis of 2H-Pyrrol-2-imines." Synthesis 51, no. 17 (May 21, 2019): 3250–58. http://dx.doi.org/10.1055/s-0037-1611830.

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2H-Pyrrol-2-imine is an important structural motif exhibiting in biologically active compounds and natural products. An efficient rhodium-catalyzed one-pot reaction of one vinyl azide with sequentially with two different isocyanides is reported, which offers an alternative facile access to 3-amino-5-aryl-2H-pyrrol-2-imines bearing various substitution on the nitrogens in good yields. An unstable vinylcarbodiimide is the key intermediate in this cascade reaction.
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44

Cibian, Mihaela, André Bessette, Andrew O'Connor, Janaina G. Ferreira, and Garry S. Hanan. "Twofac-tricarbonylrhenium(I) azadipyrromethene (ADPM) complexes: ligand-substitution effect on crystal structure." Acta Crystallographica Section C Structural Chemistry 71, no. 2 (January 17, 2015): 122–27. http://dx.doi.org/10.1107/s2053229614027673.

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The crystal structures offac-(acetonitrile-κN)(2-{[3,5-bis(4-methoxyphenyl)-2H-pyrrol-2-ylidene-κN1]amino}-3,5-bis(4-<!?tlsb=0.2pt>methoxyphenyl)-1H-pyrrol-1-ido-κN1)tricarbonylrhenium(I)–hexane–acetonitrile (2/1/2), [Re(C36H30N3O4)(CH3CN)(CO)3]·0.5C6H14·CH3CN, (2), andfac-(2-{[3,5-bis(4-methoxyphenyl)-2H-pyrrol-2-ylidene-κN1]amino}-3,5-bis(4-methoxyphenyl)-1H-pyrrol-1-ido-κN1)tricarbonyl(dimethyl sulfoxide-κO)rhenium(I), [Re(C36H30N3O4)(C2H6OS)(CO)3], (3), at 150 K are reported. Both complexes display a distorted octahedral geometry, with afac-Re(CO)3arrangement and one azadipyrromethene (ADPM) chelating ligand in the equatorial position. One solvent molecule completes the coordination sphere of the ReIcentre in the remaining axial position. The ADPM ligand shows high flexibility upon coordination, while retaining its π-delocalized nature. Bond length and angle analyses indicate that the differences in the geometry around the ReIcentre in (2) and (3), and those found in three reportedfac-Re(CO)3–ADPM complexes, are dictated mainly by steric factors and crystal packing. Both structures display intramolecular C—H...N hydrogen bonding. Intermolecular interactions of the Csp2—H...π and Csp2—H...O(carbonyl) types link the discrete monomers into extended chains.
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45

Walbank, F. W., Tony Hackens, Nancy D. Holloway, R. Ross Holloway, and Ghislaine Moucharte. "The Age of Pyrrhus." American Journal of Archaeology 100, no. 2 (April 1996): 442. http://dx.doi.org/10.2307/506934.

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46

Armour-Garb, B., and G. Priest. "Analetheism: a Pyrrhic victory." Analysis 65, no. 2 (April 1, 2005): 167–73. http://dx.doi.org/10.1093/analys/65.2.167.

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47

Isaacs, John. "MX: Reagan's pyrrhic victory?" Bulletin of the Atomic Scientists 41, no. 6 (June 1985): 4–6. http://dx.doi.org/10.1080/00963402.1985.11455972.

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48

Knight, Sarah. "Pyrrhus and the Tiger." MLN 135, no. 5 (2020): 1062–77. http://dx.doi.org/10.1353/mln.2020.0075.

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49

Habetzeder, Julia. "Dancing with decorum. The eclectic usage of kalathiskos dancers and pyrrhic dancers in Roman visual culture." Opuscula. Annual of the Swedish Institutes at Athens and Rome 5 (November 2012): 7–47. http://dx.doi.org/10.30549/opathrom-05-02.

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Abstract:
This article examines two groups of motifs in Roman visual culture: females modelled on kalathiskos dancers, and males modelled on pyrrhic dancers. Eclecticism is emphasized as a strategy which was used to introduce novelties that were appropriate within a Roman cultural context. The figures representing kalathiskos dancers and pyrrhic dancers were both changed in an eclectic manner and this resulted in motifs representing the goddess Victoria, and the curetes respectively. Kalathiskos dancers and eclectic Victoriae occur on many different media at least from the Augustan era and into the 2nd century AD. It is argued here that the establishment of these two motifs in Roman visual culture is closely related to the aesthetics which came to the fore during the reign of Augustus. Thereafter, both kalathiskos dancers and eclectic Victoriae lingered on in the Roman cultural context until many of the material categories on which they were depicted ceased to be produced. Unlike the kalathiskos dancers, the male figures modelled on pyrrhic dancers are so rare within Roman visual culture that we can only assume they were, to some extent, perceived as an inappropriate motif. This can most likely be explained by the negative attitude, amongst the Roman elite, towards male dancing.
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Beattie, Nicola J., Craig L. Francis, Andris J. Liepa, and G. Paul Savage. "Spiroheterocycles via Regioselective Cycloaddition Reactions of Nitrile Oxides with 5-Methylene-1H-pyrrol-2(5H)-ones." Australian Journal of Chemistry 63, no. 3 (2010): 445. http://dx.doi.org/10.1071/ch09479.

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Substituted 5-methylene-1H-pyrrol-2(5H)-ones underwent a 1,3-dipolar cycloaddition reaction with nitrile oxides to give the corresponding spiro heterocycles. Critical to this reaction was the development of a biphasic system for base-induced dehydrohalogenation of hydroximoyl chlorides, to give nitrile oxides, in the presence of a base-sensitive dipolarophile. A substituted N-tolyl 5-methylene-1H-pyrrol-2(5H)-one exhibited atropisomerism, which in turn led to a 4:1 facial selectivity during cycloaddition.
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