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Journal articles on the topic 'Moldavian S.S.R'

Author: Grafiati

Published: 4 June 2021

Last updated: 28 July 2025

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1

Michał, Wasiucionek. "Garments, Signatures, and Ottoman Self-Fashioning in the Imperial Periphery: Moldavian Voyvode Ştefan Tomşa II and Ottomanization in the Early Seventeenth Century." Journal of Early Modern History 24, 2020, no. 4-5 (2020): 317–40. https://doi.org/10.1163/15700658-12342659.

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The paper examines the strategies of self-representation pursued by Moldavian Voyvode Ștefan Tomșa II (r. 1611-1615, 1621-1623). From his ascension to the throne, Tomșa faced accusations of wholesale adoption of Ottoman customs and fashion, and even conversion to Islam. While Romanian scholars have largely dismissed these claims as a product of hostile propaganda, the paper argues that—while remaining an Orthodox Christian—the voyvode deliberately emphasized his affinity to the Ottoman cultural idiom and presented himself to his subjects as a member of the Ottoman ruling class. By

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2

Vorobey, Tetiana, and Nataliia Nuzhyna. "INTRODUCTION OF DRACOCEPHALUM MOLDAVICA L. IN VITRO CULTURE." Bulletin of Taras Shevchenko National University of Kyiv. Series: Biology 96, no. 1 (2024): 57–62. http://dx.doi.org/10.17721/1728.2748.2024.96.57-62.

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B a c k g r o u n d . Dracocephalum moldavica L. is widely used in folk medicine in many countries of the world due to its antispasmodic, antibacterial, analgesic, sedative and anti-inflammatory properties. D. moldavica essential oil is often used in aromatherapy and cosmetology. The use of biotechnological methods for obtaining secondary plant metabolites has become increasingly popular in recent years. On the one hand, they serve as a source of substances beneficial for pharmacology, while on the other hand, aseptic microclones of medicinal plants can be utilized as model organisms to explor

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3

Letters, Migration. "Book Reviews." Migration Letters 13, no. 2 (2016): 320–27. http://dx.doi.org/10.33182/ml.v13i2.310.

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Books received:Controlling Immigration, a Global Perspective. Edited by James F. Hollifield, Philip L. Martin, Pia M. Orrenius, Stanford, California: Stanfard University Press (ISBN: 978-08047-86270).Lives in Limbo, Undocumented and Coming of Age in America. Roberto G. Gonzales. Oakland, Califronia: University of California Press (2016, ISBN: 978-0-520-287266)Strangers No More. Richard Alba and Nancy Foner. New Jersey: Princeton University Press (2015, ISBN: 978-0691-161075).Handbook of Chinese Migration Identity and Wellbeing. Edited by Robyn R. Iredale and Fei Guo, Cheltenham: Edward Elgar (

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4

Ljubin, Valerij. "La Roumanie et son entrée dans l'Union européenne : un regard de Russie." Synergies Roumanie, Nº 16 - 2021 (November 30, 2021): 69–81. https://doi.org/10.5281/zenodo.6459554.

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L’article analyse les relations entre la Russie et la Roumanie depuis la période des années 90 à nos jours. Il résume les conclusions des savants russes qui se sont penchés sur ce sujet. Les relations russo-roumaines à l’époque considérée ont connu des périodes de rapprochement et de divergence. Ces relations sont actuellement à un faible niveau. La priorité de la Roumanie était l’adhésion à l’OTAN et à l’UE et le partenariat stratégique avec les

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5

Kushnir, Viaceslav. "The Evolution Trend of the Balta Region Moldavian Population in 19th-1920’s." Analele Universităţii "Dunărea de Jos" din Galaţi Fascicula XIX Istorie 5 (December 7, 2006): 209–14. http://dx.doi.org/10.35219/history.2006.13.

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Moldavians, or Volokhi, as they were named here at the end of 18th c. - beginning of the 19th c. is one of the most numerous ethnic groups in South- East Podil’ia. On the northern territory of the present-day Odessa and Transdniestria regions within the limits of the present-day Kam’ansk and Rybniza districts of Moldova, which were a part of the Balta povit (district), Moldavians lived both in separate monoethnic and in mixed Ukraino-Moldavian or Moldavo-Ukrainian settlements. In the early 18th c. they settled down with impetuosity on this territory together with Ukrainians. The khutors founde

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6

Eșanu, Andrei, and Valentina Eșanu. "FILIP MOLDOVEANUL (?-1553) ȘI ÎNCEPUTURILE SCRISULUI ÎN LIMBA ROMÂNĂ." Magazin Bibliologic 3-4, 2021 (December 9, 2021): 145. https://doi.org/10.5281/zenodo.5769595.

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Authors revive the personality and work of Filip Moldoveanul (Philip the Moldavian; ? -1554/1555). Based on the earlier researches, in this study his biography is readjusted and explained. The authors emphasize Filip’s Moldavian origin, his supposedly Western academic formation, similarly, his printing activity in Sibiu. New facts and nuances are objectified regarding his printings and, especially, his first Romanian translation of the Gospel and its influence on the Romanian culture. Filip Moldoveanul’s three printing works, created between 1544 and 1553, are described in detail;

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7

Azab Abd-Allah, M., Kamal El-Saady, and A. Ghareeb. "(r,s)(r,s)-Fuzzy FF-open sets and (r,s)(r,s)-fuzzy FF-closed spaces." Chaos, Solitons & Fractals 42, no. 2 (2009): 649–56. http://dx.doi.org/10.1016/j.chaos.2009.01.031.

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8

Wu, An-Hui, Chun-Kit Hau, and Henry N. C. Wong. "Synthesis of Enantiopure (S,R,S)- and (R,S,R)-1,4,5,8,9,16-Hexahydroxytetraphenylenes." Advanced Synthesis & Catalysis 349, no. 4-5 (2007): 601–8. http://dx.doi.org/10.1002/adsc.200600499.

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9

Lopez de Diego, H. "(R,S)-1-Phenylethylammonium (R,S)-Mandelate." Acta Crystallographica Section C Crystal Structure Communications 51, no. 5 (1995): 935–37. http://dx.doi.org/10.1107/s010827019401303x.

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10

Braga, Dario, Fabrizia Grepioni, and Giulio I. Lampronti. "Supramolecular metathesis: co-former exchange in co-crystals of pyrazine with (R,R)-, (S,S)-, (R,S)- and (S,S/R,R)-tartaric acid." CrystEngComm 13, no. 9 (2011): 3122–24. http://dx.doi.org/10.1039/c0ce00576b.

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11

Zhou, Jianguang, Ye Zhu, and Kevin Burgess. "Synthesis of (S,R,R,S,R,S)-4,6,8,10,16,18- Hexamethyldocosane fromAntitrogusparvulusvia Diastereoselective Hydrogenations." Organic Letters 9, no. 7 (2007): 1391–93. http://dx.doi.org/10.1021/ol070298z.

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12

Serbian, Immo, Jana Wiese, Anja Raschke, Holger B. Deising, and René Csuk. "Streamlined synthesis of (R, R)-rhizoferrin, (S, S)-rhizoferrin and (R, S, R)-staphyloferrin A." Phytochemistry Letters 33 (October 2019): 64–69. http://dx.doi.org/10.1016/j.phytol.2019.07.012.

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13

Jeschke, Peter, Jordi Benet-Buchholz, Achim Harder, Winfried Etzel, Michael Schindler, and Gerhard Thielking. "Synthesis and anthelmintic activity of cyclohexadepsipeptides with (S,S,S,R,S,R)-configuration." Bioorganic & Medicinal Chemistry Letters 13, no. 19 (2003): 3285–88. http://dx.doi.org/10.1016/s0960-894x(03)00688-7.

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14

Brunner, Henri, Manfred Muschiol, and Manfred Zabel. "Synthesis of (R,R)- and (S,S)-Norphos." Synthesis 2008, no. 3 (2008): 405–8. http://dx.doi.org/10.1055/s-2008-1032133.

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15

Hayat, Umar. "The Cramer varieties Cr(r,r+s,s)." Journal of Geometry and Physics 79 (May 2014): 53–58. http://dx.doi.org/10.1016/j.geomphys.2014.02.001.

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16

Furedy, JohnJ. "Pavlovian autonomic conditioning: S-R and S-S?" Biological Psychology 23, no. 1 (1986): 97–98. http://dx.doi.org/10.1016/0301-0511(86)90129-8.

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17

Kenton, Nathaniel T., Daniel Adu‐Ampratwum, Antony A. Okumu, et al. "Stereochemical Definition of the Natural Product (6 R ,10 R ,13 R , 14 R ,16 R ,17 R ,19 S ,20 S ,21 R ,24 S ,25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses." Angewandte Chemie 130, no. 3 (2017): 818–21. http://dx.doi.org/10.1002/ange.201711008.

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18

Kenton, Nathaniel T., Daniel Adu‐Ampratwum, Antony A. Okumu, et al. "Stereochemical Definition of the Natural Product (6 R ,10 R ,13 R , 14 R ,16 R ,17 R ,19 S ,20 S ,21 R ,24 S ,25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 by Total Synthesis and Comparative Analyses." Angewandte Chemie International Edition 57, no. 3 (2018): 810–13. http://dx.doi.org/10.1002/anie.201711008.

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19

RASMUSSEN, L., K. OLSEN, and S. JOHANSEN. "Chiral separation and quantification of R/S-amphetamine, R/S-methamphetamine, R/S-MDA, R/S-MDMA, and R/S-MDEA in whole blood by GC-EI-MS." Journal of Chromatography B 842, no. 2 (2006): 136–41. http://dx.doi.org/10.1016/j.jchromb.2006.05.011.

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20

Kenton, Nathaniel T., Daniel Adu‐Ampratwum, Antony A. Okumu, et al. "Total Synthesis of (6 R ,10 R ,13 R ,14 R ,16 R ,17 R ,19 S ,20 R ,21 R ,24 S , 25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product." Angewandte Chemie 130, no. 3 (2017): 813–17. http://dx.doi.org/10.1002/ange.201711006.

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21

Kenton, Nathaniel T., Daniel Adu‐Ampratwum, Antony A. Okumu, et al. "Total Synthesis of (6 R ,10 R ,13 R ,14 R ,16 R ,17 R ,19 S ,20 R ,21 R ,24 S , 25 S ,28 S ,30 S ,32 R ,33 R ,34 R ,36 S ,37 S ,39 R )‐Azaspiracid‐3 Reveals Non‐Identity with the Natural Product." Angewandte Chemie International Edition 57, no. 3 (2018): 805–9. http://dx.doi.org/10.1002/anie.201711006.

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22

Suareo, F. O., and K. C. Gupta. "Design of Quick-Returning R-S-S-R Mechanisms." Journal of Mechanisms, Transmissions, and Automation in Design 110, no. 4 (1988): 423–28. http://dx.doi.org/10.1115/1.3258939.

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An algebraic method is presented to synthesize quick-returning R-S-S-R mechanisms which satisfy the given time-ratio and follower oscillation angle requirements. In these designs, the three parameters, which define the follower spheric joint, satisfy a quadratic condition. When the shaft angle between the input and output shafts is zero, this quadratic condition reduces to the equation of a circle which is a familiar classical result for the planar case. The solution space for the quick-returning R-S-S-R linkage is such that, for each set of choices for crank length a2, follower axial distance

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23

Abdou, Mohamed, Christoph Kratky, and Georg Uray. "Crystal structure of (S,S)-diphenylethanediammonium (R,R)-tartrate." Monatshefte f�r Chemie Chemical Monthly 121, no. 12 (1990): 1039–43. http://dx.doi.org/10.1007/bf00809254.

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24

Remmel, Jeffrey B. "Formulas for the expansion of the Kronecker products S(m, n) ⊗ S(1p−r, r) and S(1k2l) ⊗ S(1p−r, r)." Discrete Mathematics 99, no. 1-3 (1992): 265–87. http://dx.doi.org/10.1016/0012-365x(92)90376-q.

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25

Lopez de Diego, H. "(R,S)-1-Phenylethylammonium (S)-mandelate." Acta Crystallographica Section C Crystal Structure Communications 50, no. 12 (1994): 1995–98. http://dx.doi.org/10.1107/s0108270194003884.

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26

Trench, William F. "Characterization and Properties of (R,S)-Symmetric, (R,S)-Skew Symmetric, and (R,S)-Conjugate Matrices." SIAM Journal on Matrix Analysis and Applications 26, no. 3 (2005): 748–57. http://dx.doi.org/10.1137/s089547980343134x.

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27

Brement, Marshall. "U. S.-U. S. S. R.: Possibilities in Partnership." Foreign Policy, no. 84 (1991): 107. http://dx.doi.org/10.2307/1148785.

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28

Ennis, Michael D., and Mark E. Baze. "Asymmetric total synthesis of 14(R),15(S)-, 14(S),15(R)-, 14(R),15(R)-, and 14(S),15(S)-epoxyeicosatrienoic acids." Tetrahedron Letters 27, no. 50 (1986): 6031–34. http://dx.doi.org/10.1016/s0040-4039(00)85390-3.

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29

Pekin, Ayten, Ünsal Tekir, and Özge Kılıç. "S-Semiprime Submodules and S -Reduced Modules." Journal of Mathematics 2020 (October 20, 2020): 1–7. http://dx.doi.org/10.1155/2020/8824787.

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This article introduces the concept of S -semiprime submodules which are a generalization of semiprime submodules and S -prime submodules. Let M be a nonzero unital R-module, where R is a commutative ring with a nonzero identity. Suppose that S is a multiplicatively closed subset of R . A submodule P of M is said to be an S -semiprime submodule if there exists a fixed s ∈ S , and whenever r n m ∈ P for some r ∈ R , m ∈ M , and n ∈ ℕ , then srm ∈ P . Also, M is said to be an S -reduced module if there exists (fixed) s ∈ S , and whenever r n m = 0 for some r ∈ R , m ∈ M , and n ∈ ℕ , then srm =

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30

Amiel, Gérard. "R S I." La revue lacanienne 13, no. 2 (2012): 73. http://dx.doi.org/10.3917/lrl.122.073.

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31

Enders, Dieter, Evelyn Peiffer, and Gerhard Raabe. "Asymmetric Synthesis of (S,S)- and (R,R)-2-Methylthreitol." Synthesis 2007, no. 7 (2007): 1021–26. http://dx.doi.org/10.1055/s-2007-965967.

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32

Sun, Li, and Enlin Yang. "On the GL(r)×GL(r+s)×GL(s) convolution." Journal of Number Theory 134 (January 2014): 130–41. http://dx.doi.org/10.1016/j.jnt.2013.08.001.

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33

Lee, Eun-Pyo, and Seung-Hoon Kim. "Fuzzy strongly (r, s)-semicontinuous, fuzzy strongly (r, s)-semiopen and fuzzy strongly (r, s)-semiclosed mappings." International Journal of Fuzzy Logic and Intelligent Systems 7, no. 2 (2007): 120–26. http://dx.doi.org/10.5391/ijfis.2007.7.2.120.

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34

Schanz, Hans-Jörg, Michael A. Linseis, and Declan G. Gilheany. "Improved resolution methods for (R,R)- and (S,S)-cyclohexane-1,2-diamine and (R)- and (S)-BINOL." Tetrahedron: Asymmetry 14, no. 18 (2003): 2763–69. http://dx.doi.org/10.1016/s0957-4166(03)00586-x.

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35

BEJENARU, Alexandru. "Manoil Grecul, Teodoryk Buczacki şi implicarea lor în relaţiile moldo-poloneze/Manoil Grecul, Teodoryk Buczacki and Their Involvement in Polish-Moldavian Relationships." Analele Universităţii "Dunărea de Jos" din Galaţi Fascicula XIX Istorie 19 (June 8, 2021): 23–28. http://dx.doi.org/10.35219/history.2020.02.

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In the following study the main point of discussion represents the roles of Manoil Grecul (the pârcălab of Hotin fortress between 1438-1455) and Teodoryk Buczacki (the castellan and starosta of Kamieniec between 1442-1455 and one of the most influent Polish nobles in Podolia) in the relationships between the Kingdom of Poland and the Moldavian Principality during the middle of 15th century. Both officials would become key-figures in the Polish-Moldavian contacts, because of the internal political struggle in Moldova and of the circumstances of Władysław III Warneńczyk‟s reign (1434-1444) and t

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36

Dembele, Bintou. "S/T/R/A/T/E/S." Africultures 99 - 100, no. 3 (2015): 250–61. http://dx.doi.org/10.3917/afcul.099.0250.

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37

Zeitouni, Ofer. "A Conversation with S. R. S. Varadhan." Statistical Science 33, no. 1 (2018): 126–37. http://dx.doi.org/10.1214/17-sts634.

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38

Bhatia, Rajendra. "A Conversation with S. R. S. Varadhan." Mathematical Intelligencer 30, no. 2 (2008): 24–42. http://dx.doi.org/10.1007/bf02985734.

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39

ZHANG, SHOU-YUAN. "Polynomial matrix fraction P(s)Q −1(s)R(s)." International Journal of Control 46, no. 3 (1987): 833–40. http://dx.doi.org/10.1080/00207178708547396.

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40

Vysyaraju, Ravikanth, Hanumantha Rao B., Subramanyeswara Rao I. V., Venkateswarlu J., Prasada Rao K. V. V., and Siddaiah V.*. "A Novel Process for the Preparation of [(R,S)/(S,R)] and [(S,S)/(R,R)] Chroman epoxides, Key Intermediates in the Synthesis of Nebivolol." International Journal of Bioassays 6, no. 06 (2017): 5420. http://dx.doi.org/10.21746/ijbio.2017.06.007.

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A novel, cost effective, scalable process for the preparation of chroman epoxides starting from 4-fluorophenol is described. The highlights of the process are single step O-acylation, fries rearrangement, one pot synthesis of claisen condensation, cyclization, reduction, epoxidation with over all yield of 50.9% [(R,S)/(S,R)]-chroman epoxide-A is 33.9% and [(S,S)/(R,R)]-chroman epoxide-B is 17%.

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41

Kwak, Chee-Hun, Hyejin Nam, Hye-In Kim, Min-Jeong Park, Joo-Eun Jee, and Jinkwon Kim. "Preparation, properties and crystal structure of two isomers of R,R,S,S- and R,S,R,S-[chloro(1,3,10,12,16,19-hexaazatetracyclo[17,3,1,112,16,04,9]tetracosane)copper(II)]+." Inorganica Chimica Acta 357, no. 5 (2004): 1325–31. http://dx.doi.org/10.1016/j.ica.2003.12.007.

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42

Salikhov, Vladislav K., and Mariya G. Bashmakova. "On rational approximations for some values of arctan(s∕r) for natural s and r, s < r." Moscow Journal of Combinatorics and Number Theory 11, no. 2 (2022): 181–88. http://dx.doi.org/10.2140/moscow.2022.11.181.

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43

MALCOCI, Iulia, and Ion Valer XENOFONTOV. "ACADEMICIAN ANATOLI KOVARSKI, ONE OF THE FOUNDERS OF THE ACADEMY OF SCIENCES OF THE MOLDAVIAN SOCIALIST SOVIET REPUBLIC." Akademos 1 (March 15, 2019): 98–103. https://doi.org/10.5281/zenodo.2907692.

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The study is dedicated to agronomist Anatoli Kovarsky (1904-1974), founding member of the Academy of Sciences of the Moldavian SSR. Special emphasis was placed on archival materials, iconographic sources, which develop new aspects of the scientist’s scientific and private biography. The scientific activity of the researcher was carried out in parallel with the didactic and administrative one.

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44

Kemp, Steven M. "R-S AND S(-O)-R: ALTERNATIVE DESIGNS FOR NEURAL NETWORKS." Journal of the Experimental Analysis of Behavior 67, no. 2 (1997): 229–31. http://dx.doi.org/10.1901/jeab.1997.67-229.

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45

Abbas, S. E., and W. K. Min. "(r,s)-fuzzy minimal structures and (r,s)-fuzzy minimal spaces." Journal of Intelligent & Fuzzy Systems 25, no. 3 (2013): 627–33. http://dx.doi.org/10.3233/ifs-120669.

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46

Kopylova, Natalia A., Oleksandr O. Grygorenko, Igor V. Komarov, and Ulrich Groth. "Synthesis of enantiopure (R,R)- and (S,S)-cis-2,3-propanoprolines." Tetrahedron: Asymmetry 21, no. 23 (2010): 2868–71. http://dx.doi.org/10.1016/j.tetasy.2010.11.017.

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47

Enders, Dieter, and Anja Kaiser. "Asymmetric Synthesis of (R,S)-Dehydroiridodial, (R,S)-Dehydroiridodiol and Analogues." Liebigs Annalen 1997, no. 3 (1997): 485–93. http://dx.doi.org/10.1002/jlac.199719970308.

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48

Mak, Adrian Matthew, Ralf Steudel, and Ming Wah Wong. "Homolytic SS Bond Dissociation of 11 Bis(thiocarbonyl)disulfides R-C(S)SSC(S)R and Prediction of A Novel Rubber Vulcanization Accelerator." Chemistry – An Asian Journal 3, no. 6 (2008): 1026–34. http://dx.doi.org/10.1002/asia.200800036.

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49

Mente, Nolan R., Andrew J. Wiemer, Jeffrey D. Neighbors, John A. Beutler, Raymond J. Hohl, and David F. Wiemer. "Total synthesis of (R,R,R)- and (S,S,S)-schweinfurthin F: Differences of bioactivity in the enantiomeric series." Bioorganic & Medicinal Chemistry Letters 17, no. 4 (2007): 911–15. http://dx.doi.org/10.1016/j.bmcl.2006.11.096.

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50

Obrecht, Daniel, Helena Karajiannis, Christian Lehmann, Peter Schönholzer, Clive Spiegler, and Klaus Müller. "An Efficient Synthesis of Optically Pure (R)- and (S)-2-(aminomethyl)alanine ((R)- and (S)-ama) and (R)- and (S)-2-(aminomethyl)leucine ((R)- and (S)-aml)." Helvetica Chimica Acta 78, no. 3 (1995): 703–14. http://dx.doi.org/10.1002/hlca.19950780317.

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