Увійти

Готові списки джерел за темами / Migidae / Статті в журналах

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Migidae.

Статті в журналах з теми "Migidae"

Автор: Grafiati

Опубліковано: 3 червня 2025

Оновлено: 31 липня 2025

Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями

Оберіть тип джерела:

Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Migidae".

Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.

Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.

Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.

1

Ferretti, Nelson, Sofía Copperi, Leonela Schwerdt, and Gabriel Pompozzi. "Another migid in the wall: natural history of the endemic and rare spider Calathotarsus simoni (Mygalomorphae: Migidae) from a hill slope in central Argentina." Journal of Natural History 48, no. 31-32 (2014): 1907–21. https://doi.org/10.1080/00222933.2014.886344.

Повний текст джерела

Анотація:

Ferretti, Nelson, Copperi, Sofía, Schwerdt, Leonela, Pompozzi, Gabriel (2014): Another migid in the wall: natural history of the endemic and rare spider Calathotarsus simoni (Mygalomorphae: Migidae) from a hill slope in central Argentina. Journal of Natural History 48 (31-32): 1907-1921, DOI: 10.1080/00222933.2014.886344, URL: http://dx.doi.org/10.1080/00222933.2014.886344

Стилі APA, Harvard, Vancouver, ISO та ін.

2

Ferretti, Nelson E., Duniesky Ríos-Tamayo, and Pablo A. Goloboff. "Four new species of Goloboffia (Mygalomorphae: Migidae) from Chile." Zootaxa 4712, no. 2 (2019): 251–68. https://doi.org/10.11646/zootaxa.4712.2.5.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

3

Montenegro, Vargas Rubén, and Milenko A. Aguilera. "Una nueva especie de araña trampilla del género Goloboffia Griswold y Ledford, 2001 (Araneae: Migidae) para la Región de Coquimbo, Chile." Revista Chilena de Entomología 48, no. 3 (2022): 549–58. https://doi.org/10.35249/rche.48.3.22.09.

Повний текст джерела

Анотація:

Montenegro Vargas, Rubén, Aguilera, Milenko A. (2022): Una nueva especie de araña trampilla del género Goloboffia Griswold y Ledford, 2001 (Araneae: Migidae) para la Región de Coquimbo, Chile. Revista Chilena de Entomología (Rev. Chil. Entomol.) 48 (3): 549-558, DOI: 10.35249/rche.48.3.22.09, URL: http://dx.doi.org/10.35249/rche.48.3.22.09

Стилі APA, Harvard, Vancouver, ISO та ін.

4

FERRETTI, NELSON E., DUNIESKY RÍOS-TAMAYO, and PABLO A. GOLOBOFF. "Four new species of Goloboffia (Mygalomorphae: Migidae) from Chile." Zootaxa 4712, no. 2 (2019): 251–68. http://dx.doi.org/10.11646/zootaxa.4712.2.5.

Повний текст джерела

Анотація:

The spider family Migidae Simon, 1889 is represented in Chile by three genera: Calathotarsus Simon, 1903, Mallecomigas Goloboff & Platnick, 1987 and Goloboffia Griswold & Ledford, 2001. In the present study, four new species of Goloboffia from Chile are described, increasing the known diversity and geographic distribution of the genus. Goloboffia megadeth sp. nov. and G. pachelbeli sp. nov., are described based on males and females; Goloboffia griswoldi sp. nov. and G. biberi sp. nov. are known only by females.

Стилі APA, Harvard, Vancouver, ISO та ін.

5

Ferretti, Nelson, Gabriel Pompozzi, and Pedro Cardoso. "Species conservation profile of the rare and endemic trapdoor spider Calathotarsus simoni (Araneae, Migidae) from Central Argentina." Biodiversity Data Journal 5 (October 24, 2017): e14790. https://doi.org/10.3897/BDJ.5.e14790.

Повний текст джерела

Анотація:

<i>Calathotarsus simoni</i> Schiapelli & Gerschman 1975 is the only species of Migidae in Argentina. It is a rare and endemic spider only found in relict grassland of mountain systems in the province of Buenos Aires. This species is a habitat specialist spider occupying specific areas with certain microclimatic conditions on hilly and rocky grassland areas at about 500-1500 meters above sea level. The observed extent of occurrence (EOO) is 7207 km<sup>2</sup> and the area of occupancy (AOO) is 16 km<sup>2</sup>. Two locations are identified based on the threat event related to the invasion

Стилі APA, Harvard, Vancouver, ISO та ін.

6

Ferretti, Nelson E., Daniela S. Soresi, Alda González, and Miquel Arnedo. "An integrative approach unveils speciation within the threatened spider Calathotarsus simoni (Araneae: Mygalomorphae: Migidae)." Systematics and Biodiversity 17, no. 5 (2019): 439–57. http://dx.doi.org/10.1080/14772000.2019.1643423.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

7

Ferretti, Nelson, Sofía Copperi, Leonela Schwerdt, and Gabriel Pompozzi. "Another migid in the wall: natural history of the endemic and rare spider Calathotarsus simoni (Mygalomorphae: Migidae) from a hill slope in central Argentina." Journal of Natural History 48, no. 31-32 (2014): 1907–21. http://dx.doi.org/10.1080/00222933.2014.886344.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

8

Griswold, CE. "Cladistic biogeography of afromontane spiders." Australian Systematic Botany 4, no. 1 (1991): 73. http://dx.doi.org/10.1071/sb9910073.

Повний текст джерела

Анотація:

The application of cladistic data is seen as crucial to answering questions regarding the definition, mode of origin and age of historical biogeographic patterns. From the cladograms and distributional data for four groups of afromontane spiders [Microstigmata (Microstigmatidae), the Moggridgea quercina group (Migidae), and the subfamilies Vidoleini and Phyxelidini (Amaurobiidae)] a set of nine disjunct areas of endemism is defined for African and Malagasy forests. Taxonlarea cladograms are combined through a parsimony method to produce a general area cladogram. General conclusions are: (1) Ma

Стилі APA, Harvard, Vancouver, ISO та ін.

9

Panchuk, Justina, and Nelson Ferretti. "Surface Soil Type Preference for Burrowing of the Endangered and Endemic Trapdoor SpiderCalathotarsus simoni(Araneae: Migidae)." Arachnology 17, no. 8 (2018): 364–66. http://dx.doi.org/10.13156/arac.2017.17.8.364.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

10

Main, Barbara York. "Occurrence of the trapdoor spider genusMoggridgeain Australia with descriptions of two new species (Araneae: Mygalomorphae: Migidae)." Journal of Natural History 25, no. 2 (1991): 383–97. http://dx.doi.org/10.1080/00222939100770271.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

11

Ferretti, Nelson, Gabriel Pompozzi, and Pedro Cardoso. "Species conservation profile of the rare and endemic trapdoor spider Calathotarsus simoni (Araneae, Migidae) from Central Argentina." Biodiversity Data Journal 5 (October 24, 2017): e14790. http://dx.doi.org/10.3897/bdj.5.e14790.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

12

Harvey, Mark S., Barbara York Main, Michael G. Rix, and Steven J. B. Cooper. "Refugia within refugia: in situ speciation and conservation of threatened Bertmainius (Araneae : Migidae), a new genus of relictual trapdoor spiders endemic to the mesic zone of south-western Australia." Invertebrate Systematics 29, no. 6 (2015): 511. http://dx.doi.org/10.1071/is15024.

Повний текст джерела

Анотація:

The trapdoor spider family Migidae has a classical Gondwanan distribution and is found on all southern continents except the Indian region. The Australian fauna consists of three genera including Moggridgea O. P. Cambridge from south-western Australia and Kangaroo Island, South Australia; Moggridgea is otherwise widespread throughout Africa. The sole named species of Moggridgea from Western Australia, M. tingle Main, and its unnamed relatives are the subject of the present paper, which was stimulated by concern for the long-term persistence of populations, and the discovery of deep genetic div

Стилі APA, Harvard, Vancouver, ISO та ін.

13

Montenegro Vargas, Rubén, and Milenko A. Aguilera. "Una nueva especie de araña trampilla del género Goloboffia Griswold y Ledford, 2001 (Araneae: Migidae) para la Región de Coquimbo, Chile." REVISTA CHILENA DE ENTOMOLOGÍA 48, no. 3 (2022): 549–58. http://dx.doi.org/10.35249/rche.48.3.22.09.

Повний текст джерела

Анотація:

Una nueva especie de Goloboffia Griswold y Ledford, 2001 es descrita e ilustrada, con base en ejemplares adultos de ambos sexos. Goloboffia gonzalezi sp. nov. difiere de las otras especies del género por la morfología del bulbo copulador del macho y por la espermateca de la hembra. Esta nueva especie representa el registro más septentrional para el género en el país. El taxón se caracteriza por tener exigencias ambientales específicas que las hacen exclusivas de ciertos microhábitats, convirtiéndolas en especies sensibles a los cambios ambientales y/o de hábitat.

Стилі APA, Harvard, Vancouver, ISO та ін.

14

Harrison, Sophie E., Michael G. Rix, Mark S. Harvey, and Andrew D. Austin. "An African mygalomorph lineage in temperate Australia: the trapdoor spider genus M oggridgea (Araneae: Migidae) on Kangaroo Island, South Australia." Austral Entomology 55, no. 2 (2015): 208–16. http://dx.doi.org/10.1111/aen.12172.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

15

Marsh, Jessica R., Tessa M. Bradford, and Steven J. B. Cooper. "Strong Population Genetic Structure for the Endangered Micro-Trapdoor Spider Moggridgea rainbowi (Mygalomorphae, Migidae) in Unburnt Habitat after Catastrophic Bushfires." Diversity 15, no. 7 (2023): 827. http://dx.doi.org/10.3390/d15070827.

Повний текст джерела

Анотація:

Catastrophic wildfires impacted large areas of western Kangaroo Island (KI), South Australia in 2019–2020, burning habitat for many species, including large proportions of the distributional range of the KI micro-trapdoor spider Moggridgea rainbowi, which led to it being listed as Endangered under Australia’s Environment Protection and Biodiversity Conservation Act (EPBC Act). In order to assess population genetic structure in M. rainbowi and detect diagnosable lineages and their distributional patterns across KI, 28 individuals were genotyped for 2495 loci, sampling from all known populations

Стилі APA, Harvard, Vancouver, ISO та ін.

16

COOPER, STEVEN J. B., MARK S. HARVEY, KATHLEEN M. SAINT, and BARBARA Y. MAIN. "Deep phylogeographic structuring of populations of the trapdoor spider Moggridgea tingle (Migidae) from southwestern Australia: evidence for long-term refugia within refugia." Molecular Ecology 20, no. 15 (2011): 3219–36. http://dx.doi.org/10.1111/j.1365-294x.2011.05160.x.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

17

Li, Ruoyan, Cong Luo, Junjie Zhong, et al. "Functional identification of mango MiGID1A and MiGID1B genes confers early flowering and stress tolerance." Plant Science 355 (June 2025): 112468. https://doi.org/10.1016/j.plantsci.2025.112468.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

18

Kikuchi, Norio, Shogo Arai, Goro Yoshida, et al. "Porphyra migitae sp. nov. (Bangiales, Rhodophyta) from Japan." Phycologia 49, no. 4 (2010): 345–54. http://dx.doi.org/10.2216/09-82.1.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

19

Chandrasekhar, Balla, Sudhakar Athe, P. Purushotham Reddy, and Subhash Ghosh. "Synthesis of fully functionalized aglycone of lycoperdinoside A and B." Organic & Biomolecular Chemistry 13, no. 1 (2015): 115–24. http://dx.doi.org/10.1039/c4ob01716a.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

20

NIAMA, BOUIRIG, and JINFALI. "Evolution of Migital Marketing in Africa Amid Covid-19." International Journal of Innovative Science and Research Technology 8, no. 3 (2023): 2169–74. https://doi.org/10.5281/zenodo.7811148.

Повний текст джерела

Анотація:

Digital marketing is the creation and distribution of content via websites, landing pages, social media platforms, email, and mobile applications. It also refers to the promotion of that content via a range of paid, earned, and owned digital channels, including advertising, content syndication, social, email, text messages, and more. Digital marketing strategies help marketers define goals, target an audience, and develop a digital marketing plan that best reaches that audience. These strategies provide direction for a given campaign or program and a framework for evaluating outcomes. Customer

Стилі APA, Harvard, Vancouver, ISO та ін.

21

Peng, Li-fen, Bing-hao Wang, Ming Wang, et al. "A One-Pot Method for the Synthesis of Phenylalkynyl-Substituted Terminal Alkynes by Deprotection/Stannylation followed by a Migita–Kosugi–Stille coupling." Journal of Chemical Research 42, no. 5 (2018): 235–38. http://dx.doi.org/10.3184/174751918x15258743466204.

Повний текст джерела

Анотація:

A practical one-pot approach for the synthesis of arylalkynyl-substituted terminal alkynes has been developed through a deprotection/ stannylation of a phenylethynyl phosphine oxide followed by Migita–Kosugi–Stille coupling, avoiding the longer synthetic route involving repeated deprotection/Sonogashira coupling. Other features of this approach include mild reaction conditions, excellent yields, facile isolation of products and wide functional group tolerance.

Стилі APA, Harvard, Vancouver, ISO та ін.

22

Wang, Aohan, Masanori Toyofuku, Nobuhiko Nomura, and Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation." International Letters of Chemistry, Physics and Astronomy 32 (April 2014): 62–70. http://dx.doi.org/10.18052/www.scipress.com/ilcpa.32.62.

Повний текст джерела

Анотація:

Signal molecules for quorum sensing are employed for ligands to palladium. The complex canbe used as a catalyst. Migita-Kosugi-Stille coupling reactions are driven by using a series of N-(3-oxo-acyl)-L-homoserine lactones as ligands coordinating with Pd. Catalysis of [Pd-(signal moleculesfor quorum sensing), or Pd/QS] allows production of conjugated polymers with light-emittingfunctions.

Стилі APA, Harvard, Vancouver, ISO та ін.

23

Wang, Aohan, Masanori Toyofuku, Nobuhiko Nomura, and Hiromasa Goto. "Quorum Sensing Materials as New Ligand for Palladium Catalyzed Migita-Kosugi-Stille Polycondensation." International Letters of Chemistry, Physics and Astronomy 32 (April 22, 2014): 62–70. http://dx.doi.org/10.56431/p-kk1e9q.

Повний текст джерела

Анотація:

Signal molecules for quorum sensing are employed for ligands to palladium. The complex canbe used as a catalyst. Migita-Kosugi-Stille coupling reactions are driven by using a series of N-(3-oxo-acyl)-L-homoserine lactones as ligands coordinating with Pd. Catalysis of [Pd-(signal moleculesfor quorum sensing), or Pd/QS] allows production of conjugated polymers with light-emittingfunctions.

Стилі APA, Harvard, Vancouver, ISO та ін.

24

Fürstner, Alois, Jacques-Alexis Funel, Martin Tremblay, et al. "A versatile protocol for Stille–Migita cross coupling reactions." Chemical Communications, no. 25 (2008): 2873. http://dx.doi.org/10.1039/b805299a.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

25

Probst, Nicolas, Rémy Lartia, Océane Théry, Mouâd Alami, Eric Defrancq, and Samir Messaoudi. "Efficient Buchwald-Hartwig-Migita Cross-Coupling for DNA Thioglycoconjugation." Chemistry - A European Journal 24, no. 8 (2018): 1795–800. http://dx.doi.org/10.1002/chem.201705371.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

26

Nagaki, Aiichiro, and Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow." Synthesis 53, no. 11 (2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.

Повний текст джерела

Анотація:

AbstractAryl–aryl cross-coupling reactions are important reactions for the production of various biaryl compounds. This short review covers the various aryl–aryl cross-coupling reactions carried out in flow, focusing on the metal species of the aryl nucleophiles used in the cross-coupling reactions.1 Introduction2 Suzuki–Miyaura Coupling (B)3 Migita–Kosugi–Stille Coupling (Sn)4 Negishi Coupling (Zn)5 Kumada–Tamao–Corriu Coupling (Mg)6 Murahashi Coupling (Li)7 Conclusion

Стилі APA, Harvard, Vancouver, ISO та ін.

27

Yu, Jingbo, Zikun Hong, Xinjie Yang, Yu Jiang, Zhijiang Jiang, and Weike Su. "Bromide-assisted chemoselective Heck reaction of 3-bromoindazoles under high-speed ball-milling conditions: synthesis of axitinib." Beilstein Journal of Organic Chemistry 14 (April 6, 2018): 786–95. http://dx.doi.org/10.3762/bjoc.14.66.

Повний текст джерела

Анотація:

A mechanically-activated chemoselective Heck coupling for the synthesis of 3-vinylindazoles has been developed with the aid of catalytic amounts of TBAB and NaBr as both dehalogenation restrainer and grinding auxiliary. After tuning of the chemical conditions and mechanical parameters, a series of non-activated 3-bromoindazoles and a broad scope of olefins worked well to give the corresponding coupling products in good to excellent yields. A further application of this protocol was performed in a two-step mechanochemical Heck/Migita cross coupling, which provided a highly efficient route for t

Стилі APA, Harvard, Vancouver, ISO та ін.

28

Gatwaza, Olivier Clement, Xin Cao, and Mukete Beckline. "Impact of Urbanization on the Hydrological Cycle of Migina Catchment, Rwanda." OALib 03, no. 07 (2016): 1–12. http://dx.doi.org/10.4236/oalib.1102830.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

29

Wang, Xiu, Zhenhua Wang, Li Liu, Yuya Asanuma, and Yasushi Nishihara. "Nickel-Catalyzed Decarbonylative Stannylation of Acyl Fluorides under Ligand-Free Conditions." Molecules 24, no. 9 (2019): 1671. http://dx.doi.org/10.3390/molecules24091671.

Повний текст джерела

Анотація:

Nickel-catalyzed decarbonylative stannylation of acyl fluorides under ligand-free conditions was disclosed. A variety of aromatic acyl fluorides are capable of reacting with silylstannanes in the presence of cesium fluoride. A one-pot decarbonylative stannylation/Migita-Kosugi-Stille reaction of benzoyl fluoride, giving rise to the direct formation of the corresponding cross-coupled products, further demonstrated the synthetic utility of the present method. This newly developed methodology with a good functional-group compatibility via C–F bond cleavage and C–Sn bond formation under nickel cat

Стилі APA, Harvard, Vancouver, ISO та ін.

30

Higashihara, Tomoya. "Nonstoichiometric Migita-Kosugi-Stille Coupling Polycondensation based on Intramolecular Catalyst Transfer System." Journal of Synthetic Organic Chemistry, Japan 81, no. 6 (2023): 574–81. http://dx.doi.org/10.5059/yukigoseikyokaishi.81.574.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

31

Calamante, Massimo, Gianna Reginato, Alessio Dessì, Matteo Bartolini, Lorenzo Zani, and Alessandro Mordini. "Extending the Conjugation of Pechmann Lactone Thienyl Derivatives: A New Class of Small Molecules for Organic Electronics Application." Synthesis 50, no. 06 (2017): 1284–92. http://dx.doi.org/10.1055/s-0036-1591856.

Повний текст джерела

Анотація:

The preparation and spectroscopic characterization of some symmetrical small molecules containing the disubstituted (E)-3,3′-bifuranylidene-2,2′-dione chromophore (the so-called Pechmann lactone) and featuring an extended conjugation are reported. The synthetic approach of such compounds is based on the Stille–Migita coupling reaction, which is carried out in very mild conditions, suitable to be applied with the very sensitive Pechmann core. The absorption and emission spectra of the new molecules obtained have been recorded in solution and clearly show how their photophysical properties can b

Стилі APA, Harvard, Vancouver, ISO та ін.

32

Ishikawa, Takumi, Mako Murata, Hiroshi Masai, Tomohiro Iwai, and Jun Terao. "Irradiation with UV Light Accelerates the Migita–Kosugi–Stille Coupling Reaction in Air." Chemistry Letters 51, no. 2 (2022): 124–26. http://dx.doi.org/10.1246/cl.210665.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

33

Bennai, Nedjwa, Nada Ibrahim, Jérôme Marrot, et al. "Synthesis of S-Trifluoromethyl S-Arylsulfoximine Thioglycosides through Pd-Catalyzed Migita Cross-Coupling." European Journal of Organic Chemistry 2020, no. 31 (2020): 4972–81. http://dx.doi.org/10.1002/ejoc.202000821.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

34

Munyaneza, O., A. Mukubwa, S. Maskey, J. Wenninger, and S. Uhlenbrook. "Assessment of surface water resources availability using catchment modeling and the results of tracer studies in the meso-scale Migina Catchment, Rwanda." Hydrology and Earth System Sciences Discussions 10, no. 12 (2013): 15375–408. http://dx.doi.org/10.5194/hessd-10-15375-2013.

Повний текст джерела

Анотація:

Abstract. In the last couple of years, different hydrological research projects were undertaken in the Migina catchment (243.2 km2), a tributary of the Kagera river in Southern Rwanda. These projects were aimed to understand hydrological processes of the catchment using analytical and experimental approaches and to build a pilot case whose experience can be extended to other catchments in Rwanda. In the present study, we developed a hydrological model of the catchment, which can be used to inform water resources planning and decision making. The semi-distributed hydrological model HEC-HMS (ver

Стилі APA, Harvard, Vancouver, ISO та ін.

35

Franchi, Daniele, Massimo Calamante, Carmen Coppola, et al. "Synthesis and Characterization of New Organic Dyes Containing the Indigo Core." Molecules 25, no. 15 (2020): 3377. http://dx.doi.org/10.3390/molecules25153377.

Повний текст джерела

Анотація:

A new series of symmetrical organic dyes containing an indigo central core decorated with different electron donor groups have been prepared, starting from Tyrian Purple and using the Pd-catalyzed Stille-Migita coupling process. The effect of substituents on the spectroscopic properties of the dyes has been investigated theoretically and experimentally. In general, all dyes presented intense light absorption bands, both in the blue and red regions of the visible spectrum, conferring them a bright green color in solution. Using the same approach, an asymmetrically substituted D–A-π–A green dye,

Стилі APA, Harvard, Vancouver, ISO та ін.

36

Kratochvíl, Jiří, Zdeněk Novák, Mukund Ghavre, et al. "Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita–Stille Coupling of Iodoacrylates." Organic Letters 17, no. 3 (2015): 520–23. http://dx.doi.org/10.1021/ol5035113.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

37

Andrade, Maria Aparecida de O. G., and Thaís Grossi Andrade. "O DUTY TO MIGITATE THE LOSS NO BRASIL: O DEVER DO CREDOR DE MITIGAR SEU PROPRIO PREJUÍZO." Conecta - Revista Interdisciplinar da Faculdade Arnaldo Janssen 1, no. 1 (2023): 123–42. http://dx.doi.org/10.60033/conecta.v1i1.5.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

38

Yano, Hiroki, Yui Nakajima, and Yasushi Obora. "N,N-Dimethylformamide-stabilized palladium nanoclusters as catalyst for Migita–Kosugi–Stille cross-coupling reactions." Journal of Organometallic Chemistry 745-746 (November 2013): 258–61. http://dx.doi.org/10.1016/j.jorganchem.2013.08.004.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

39

Zhu, Mingxiang, Mouad Alami, and Samir Messaoudi. "Electrochemical nickel-catalyzed Migita cross-coupling of 1-thiosugars with aryl, alkenyl and alkynyl bromides." Chemical Communications 56, no. 32 (2020): 4464–67. http://dx.doi.org/10.1039/d0cc01126f.

Повний текст джерела

Анотація:

An efficient electrochemical route towards the synthesis of thioglycosides is reported. This approach involves a S–C cross-coupling from protected and unprotected thiosugars with aryl bromides under base free conditions.

Стилі APA, Harvard, Vancouver, ISO та ін.

40

Krause, André, Alexander Hertl, Fabian Muttach, and Andres Jäschke. "Phosphine-Free Stille-Migita Chemistry for the Mild and Orthogonal Modification of DNA and RNA." Chemistry - A European Journal 20, no. 50 (2014): 16613–19. http://dx.doi.org/10.1002/chem.201404843.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

41

Campos, Joana F., and Sabine Berteina-Raboin. "Eucalyptol as bio-based solvent for Migita–Kosugi–Stille coupling reaction on O,S,N-heterocycle." Catalysis Today 358 (December 2020): 138–42. http://dx.doi.org/10.1016/j.cattod.2019.11.004.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

42

Dowlut, Meenakshi, Debasis Mallik, and Michael G Organ. "An Efficient Low-Temperature Stille-Migita Cross-Coupling Reaction for Heteroaromatic Compounds by Pd-PEPPSI-IPent." Chemistry - A European Journal 16, no. 14 (2010): 4279–83. http://dx.doi.org/10.1002/chem.200903337.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

43

Kratochvil, Jiri, Zdenek Novak, Mukund Ghavre, et al. "ChemInform Abstract: Fully Substituted Pyranones via Quasi-Heterogeneous Genuinely Ligand-Free Migita-Stille Coupling of Iodoacrylates." ChemInform 46, no. 28 (2015): no. http://dx.doi.org/10.1002/chin.201528186.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

44

Ansari, Nurul N., Matthew M. Cummings, and Björn C. G. Söderberg. "Chemoselectivity in the Kosugi-Migita-Stille coupling of bromophenyl triflates and bromo-nitrophenyl triflates with (ethenyl)tributyltin." Tetrahedron 74, no. 21 (2018): 2547–60. http://dx.doi.org/10.1016/j.tet.2018.02.051.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

45

Yano, Hiroki, Yui Nakajima, and Yasushi Obora. "ChemInform Abstract: N,N-Dimethylformamide-Stabilized Palladium Nanoclusters as Catalyst for Migita-Kosugi-Stille Cross-Coupling Reactions." ChemInform 45, no. 14 (2014): no. http://dx.doi.org/10.1002/chin.201414040.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

46

Regassa, Megersa, Terefe Mitiku, and Waktole Hailu. "Addooyyee: Girl’s Indigenous Friendship Institution in Oromoo, Ethiopia." International Journal of Multicultural and Multireligious Understanding 6, no. 1 (2019): 307. http://dx.doi.org/10.18415/ijmmu.v6i1.620.

Повний текст джерела

Анотація:

This thesis explores the role of the addooyyee institution in making friendship and sisterhood relation among girls. It aims at discussing the procedure by which addooyyee established between girls and used as girls’ friendship. During data collection, ethnographic methods such as observation, focus group discussions and semi-structured interview were employed. In data analysis, interpretive method was used to discuss the collected data. The analyzed data shows that, the addooyyee institution has vital role in making friendship and sisterhood relation among girls in their social, economic and

Стилі APA, Harvard, Vancouver, ISO та ін.

47

Dowlut, Meenakshi, Debasis Mallik, and Michael G. Organ. "ChemInform Abstract: An Efficient Low-Temperature Stille-Migita Cross-Coupling Reaction for Heteroaromatic Compounds by Pd-PEPPSI-IPent." ChemInform 41, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.201035049.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

48

Terayama, Kosuke, Chuan-Wen Liu, and Tomoya Higashihara. "Catalyst-transfer system in stoichiometry-independent AA+BB-type Migita–Kosugi–Stille coupling polycondensation using ester-functionalized dibromo monomer." Polymer Journal 54, no. 2 (2021): 143–50. http://dx.doi.org/10.1038/s41428-021-00571-2.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

49

Izgu, Enver Cagri, and Thomas R. Hoye. "o-(Trialkylstannyl)anilines and their utility in Migita–Kosugi–Stille cross-coupling: direct introduction of the 2-aminophenyl substituent." Tetrahedron Letters 53, no. 37 (2012): 4938–41. http://dx.doi.org/10.1016/j.tetlet.2012.06.138.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

50

Uwimana, Abias, Anne A. van Dam, Gretchen M. Gettel, and Kenneth Irvine. "Effects of agricultural land use on sediment and nutrient retention in valley-bottom wetlands of Migina catchment, southern Rwanda." Journal of Environmental Management 219 (August 2018): 103–14. http://dx.doi.org/10.1016/j.jenvman.2018.04.094.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

Ми пропонуємо знижки на всі преміум-плани для авторів, чиї праці увійшли до тематичних добірок літератури. Зв'яжіться з нами, щоб отримати унікальний промокод!