Log in

Relevant bibliographies by topics / Stille coupling reactions / Journal articles

To see the other types of publications on this topic, follow the link: Stille coupling reactions.

Journal articles on the topic 'Stille coupling reactions'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

Create a spot-on reference in APA, MLA, Chicago, Harvard, and other styles

Select a source type:

Consult the top 50 journal articles for your research on the topic 'Stille coupling reactions.'

Next to every source in the list of references, there is an 'Add to bibliography' button. Press on it, and we will generate automatically the bibliographic reference to the chosen work in the citation style you need: APA, MLA, Harvard, Chicago, Vancouver, etc.

You can also download the full text of the academic publication as pdf and read online its abstract whenever available in the metadata.

Browse journal articles on a wide variety of disciplines and organise your bibliography correctly.

1

Pires, Marina, Sara Purificação, A. Santos, and M. Marques. "The Role of PEG on Pd- and Cu-Catalyzed Cross-Coupling Reactions." Synthesis 49, no. 11 (April 26, 2017): 2337–50. http://dx.doi.org/10.1055/s-0036-1589498.

Full text

Abstract:

Carbon–carbon and carbon–heteroatom coupling reactions are among the most important transformations in organic synthesis as they enable complex structures to be formed from readily available compounds under different routes and conditions. Several metal-catalyzed cross-coupling reactions have been developed creating many efficient methods accessible for the direct formation of new bonds between differently hybridized carbon atoms.During the last decade, much effort has been devoted towards improvement of the sustainability of these reactions, such as catalyst recovery and atom efficiency. Polyethylene glycol (PEG) can be used as a medium, as solid-liquid phase transfer catalyst, or even as a polymer support. PEG has been investigated in a wide variety of cross-coupling reactions either as an alternative solvent to the common organic solvents or as a support for catalyst, substrate, and ligand. In this review we will summarize the different roles of PEG in palladium- and copper-catalyzed cross-coupling reactions, with the focus on Heck, Suzuki–Miyaura, Sonogashira, Buchwald–Hartwig, Stille, Fukuyama, and homocoupling reactions. We will highlight the role of PEG, the preparation of PEGylated catalysts and substrates, and the importance for the reaction outcome and applicability.1 Introduction2 PEG in Heck Reactions3 PEG in Homocoupling Reactions4 PEG in Suzuki–Miyaura Reactions5 PEG in Sonogashira Reactions6 PEG in Buchwald–Hartwig Reactions7 PEG in Stille Reactions8 PEG in Fukuyama Reactions9 PEG in Miscellaneous Cross-Coupling Routes10 Conclusions

APA, Harvard, Vancouver, ISO, and other styles

2

Pattenden, Gerald, and Davey Stoker. "Stille Cross-Coupling Reactions Using Vinylcyclopropylstannanes." Synlett 2009, no. 11 (June 2, 2009): 1800–1802. http://dx.doi.org/10.1055/s-0029-1217327.

Full text

APA, Harvard, Vancouver, ISO, and other styles

3

Huang, Hongyan, Guanyuan Jiao, Shuli Liu, Quan Li, Xin Shi, Nina Fu, Lianhui Wang, Baomin Zhao, and Wei Huang. "Unprecedented side reactions in Stille coupling: desired ones for Stille polycondensation." Chemical Communications 51, no. 87 (2015): 15846–49. http://dx.doi.org/10.1039/c5cc05404d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

4

Clapham, Bruce, and Andrew J. Sutherland. "Stille Coupling Reactions of 4-Substituted-2,5-Diphenyloxazoles†." Journal of Organic Chemistry 66, no. 26 (December 2001): 9033–37. http://dx.doi.org/10.1021/jo0107150.

Full text

APA, Harvard, Vancouver, ISO, and other styles

5

Hrizi, Asma, Manon Cailler, Moufida Romdhani-Younes, Yvan Carcenac, and Jérôme Thibonnet. "Synthesis of New Highly Functionalized 1H-Indole-2-carbonitriles via Cross-Coupling Reactions." Molecules 26, no. 17 (August 31, 2021): 5287. http://dx.doi.org/10.3390/molecules26175287.

Full text

Abstract:

An approach for the preparation of polysubstituted indole-2-carbonitriles through a cross-coupling reaction of compounds 1-(but-2-ynyl)-1H-indole-2-carbonitriles and 1-benzyl-3-iodo-1H-indole-2-carbonitriles is described. The reactivity of indole derivatives with iodine at position 3 was studied using cross-coupling reactions. The Sonogashira, Suzuki–Miyaura, Stille and Heck cross-couplings afforded a variety of di-, tri- and tetra-substituted indole-2-carbonitriles.

APA, Harvard, Vancouver, ISO, and other styles

6

Quayle, Peter, Jingyang Wang, Jie Xu, and Christopher J. Urch. "Stereoselective Stille coupling reactions of 1,1-bis(trialkylstannyl)ethenes." Tetrahedron Letters 39, no. 5-6 (January 1998): 485–88. http://dx.doi.org/10.1016/s0040-4039(97)10583-4.

Full text

APA, Harvard, Vancouver, ISO, and other styles

7

Larhed, Mats, Masahide Hoshino, Sabine Hadida, Dennis P. Curran, and Anders Hallberg. "Rapid Fluorous Stille Coupling Reactions Conducted under Microwave Irradiation." Journal of Organic Chemistry 62, no. 16 (August 1997): 5583–87. http://dx.doi.org/10.1021/jo970362y.

Full text

APA, Harvard, Vancouver, ISO, and other styles

8

Fürstner, Alois, Jacques-Alexis Funel, Martin Tremblay, Laure C. Bouchez, Cristina Nevado, Mario Waser, Jens Ackerstaff, and Christopher C. Stimson. "A versatile protocol for Stille–Migita cross coupling reactions." Chemical Communications, no. 25 (2008): 2873. http://dx.doi.org/10.1039/b805299a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

9

Thiele, Christina M., and Terence N. Mitchell. "Short communication: Stille coupling reactions of functionalized triorganotin halides." Applied Organometallic Chemistry 18, no. 2 (January 28, 2004): 83–85. http://dx.doi.org/10.1002/aoc.585.

Full text

APA, Harvard, Vancouver, ISO, and other styles

10

Larson, Gerald. "Some Aspects of the Chemistry of Alkynylsilanes." Synthesis 50, no. 13 (May 18, 2018): 2433–62. http://dx.doi.org/10.1055/s-0036-1591979.

Full text

Abstract:

In amongst the considerable chemistry of acetylenes there lies some unique chemistry of alkynylsilanes (silylacetylenes) some of which is reviewed herein. This unique character is exemplified not only in the silyl protection of the terminal C–H of acetylenes, but also in the ability of the silyl group to be converted into other functionalities after reaction of the alkynylsilane and to its ability to dictate and improve the regioselectivity of reactions at the triple bond. This, when combined with the possible subsequent transformations of the silyl group, makes their chemistry highly versatile and useful.1 Introduction2 Safety3 Synthesis4 Protiodesilylation5 Sonogashira Reactions6 Cross-Coupling with the C–Si Bond7 Stille Cross-Coupling8 Reactions at the Terminal Carbon9 Cross-Coupling with Silylethynylmagnesium Bromides10 Reactions of Haloethynylsilanes11 Cycloaddition Reactions11.1 Formation of Aromatic Rings11.2 Diels–Alder Cyclizations11.3 Formation of Heterocycles11.4 Formation of 1,2,3-Triazines11.5 [2+3] Cycloadditions11.6 Other Cycloadditions12 Additions to the C≡C Bond13 Reactions at the C–Si Bond14 Miscellaneous Reactions

APA, Harvard, Vancouver, ISO, and other styles

11

Franzén, Robert. "The Suzuki, the Heck, and the Stille reaction - three versatile methods for the introduction of new C-C bonds on solid support." Canadian Journal of Chemistry 78, no. 7 (July 1, 2000): 957–62. http://dx.doi.org/10.1139/v00-089.

Full text

Abstract:

Metal-catalyzed coupling reactions are very efficient and reliable methods for the introduction of new carbon-carbon bonds onto molecules attached to a solid support. This review summarizes recent advances in utilizing the three most used methods, the Suzuki reaction, the Heck reaction, and the Stille reaction, in the field of solid phase organic synthesis resulting in small organic molecule libraries.Key words: metal-catalyzed coupling reactions, carbon-carbon bonds, solid phase synthesis, combinatorial chemistry, drug discovery.

APA, Harvard, Vancouver, ISO, and other styles

12

Sydnes, Magne O. "Green Bio-Based Solvents in C-C Cross-Coupling Reactions." Current Green Chemistry 6, no. 2 (October 25, 2019): 96–104. http://dx.doi.org/10.2174/2213346106666190411151447.

Full text

Abstract:

Solvent accounts for majority of the waste derived from synthetic transformations. This implies that by making changes to the solvent used by either switching to greener options, reducing the volume of solvent used, or even better avoiding the use of solvent totally will have a positive impact on the environment. Herein, the focus will be on the use of bio-based-green-solvents in C-C crosscoupling reactions highlighting the recent developments in this field of research. Emphasis in this review will be placed on developments obtained for Mizoroki-Heck, Hiyama, Stille, and Suzuki- Miyaura cross-couplings. For these cross-coupling reactions, good reaction conditions utilizing green solvents are now available.

APA, Harvard, Vancouver, ISO, and other styles

13

Ohtaka, Atsushi. "Transition-metal Nanoparticles Catalyzed Carbon-Carbon Coupling Reactions in Water." Current Organic Chemistry 23, no. 6 (July 4, 2019): 689–703. http://dx.doi.org/10.2174/1385272823666190419211714.

Full text

Abstract:

The use of transition-metal nanoparticles in catalysis has attracted much interest, and their use in carbon-carbon coupling reactions such as Suzuki, Heck, Sonogashira, Stille, Hiyama, and Ullmann coupling reactions constitutes one of their most important applications. The transition-metal nanoparticles are considered as one of the green catalysts because they show high catalytic activity for several reactions in water. This review is devoted to the catalytic system developed in the past 10 years in transition-metal nanoparticles-catalyzed carbon-carbon coupling reactions such as Suzuki, Heck, Sonogashira, Stille, Hiyama, and Ullmann coupling reactions in water.

APA, Harvard, Vancouver, ISO, and other styles

14

Dell’Anna, Maria Michela, Antonio Lofù, Piero Mastrorilli, Vittoria Mucciante, and Cosimo Francesco Nobile. "Stille coupling reactions catalysed by a polymer supported palladium complex." Journal of Organometallic Chemistry 691, no. 1-2 (January 2006): 131–37. http://dx.doi.org/10.1016/j.jorganchem.2005.07.104.

Full text

APA, Harvard, Vancouver, ISO, and other styles

15

Vitz, J?rgen, Dinh Hung Mac, and St?phanie Legoupy. "Ionic liquid supported tin reagents for Stille cross coupling reactions." Green Chemistry 9, no. 5 (2007): 431. http://dx.doi.org/10.1039/b616218e.

Full text

APA, Harvard, Vancouver, ISO, and other styles

16

Clapham, Bruce, and Andrew J. Sutherland. "ChemInform Abstract: Stille Coupling Reactions of 4-Substituted-2,5-diphenyloxazoles." ChemInform 33, no. 25 (May 21, 2010): no. http://dx.doi.org/10.1002/chin.200225117.

Full text

APA, Harvard, Vancouver, ISO, and other styles

17

Strueben, Jan, Paul J. Gates, and Anne Staubitz. "Tin-Functionalized Azobenzenes as Nucleophiles in Stille Cross-Coupling Reactions." Journal of Organic Chemistry 79, no. 4 (February 6, 2014): 1719–28. http://dx.doi.org/10.1021/jo402598u.

Full text

APA, Harvard, Vancouver, ISO, and other styles

18

Betzer, Jean-François. "Stille Coupling Reactions in the Preparation of Substituted Trienic Systems." Synthesis 1998, S1 (March 1998): 522–36. http://dx.doi.org/10.1055/s-1998-5936.

Full text

APA, Harvard, Vancouver, ISO, and other styles

19

Mowery, Molly E., and Philip DeShong. "Cross-Coupling Reactions of Hypervalent Siloxane Derivatives: An Alternative to Stille and Suzuki Couplings†." Journal of Organic Chemistry 64, no. 5 (March 1999): 1684–88. http://dx.doi.org/10.1021/jo982463h.

Full text

APA, Harvard, Vancouver, ISO, and other styles

20

Zhang, Xin, Long Lu, and Donald J. Burton. "The Stereoselective Preparation of Fluorinated Dienes via Stille-Liebeskind Cross-Coupling Reactions." Collection of Czechoslovak Chemical Communications 67, no. 9 (2002): 1247–61. http://dx.doi.org/10.1135/cccc20021247.

Full text

Abstract:

Readily prepared fluorinated vinylstannane reagents stereoselectively undergo Stille-Liebeskind cross-coupling reactions with vinyl halides (including fluorine-containing vinyl halides) with Pd(PPh3)4/CuI catalysis.

APA, Harvard, Vancouver, ISO, and other styles

21

Nagaki, Aiichiro, and Yosuke Ashikari. "Homogeneous Catalyzed Aryl–Aryl Cross-Couplings in Flow." Synthesis 53, no. 11 (January 18, 2021): 1879–88. http://dx.doi.org/10.1055/a-1360-7798.

Full text

Abstract:

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

APA, Harvard, Vancouver, ISO, and other styles

22

Jeanneret, Vincent, Lieven Meerpoel, and Pierre Vogel. "C-Glycosides and C-disaccharide precursors through carbonylative Stille coupling reactions." Tetrahedron Letters 38, no. 4 (January 1997): 543–46. http://dx.doi.org/10.1016/s0040-4039(96)02367-2.

Full text

APA, Harvard, Vancouver, ISO, and other styles

23

Domini, Claudia E., Gustavo F. Silbestri, Beatriz Fernández Band, and Alicia B. Chopa. "Ultrasound-assisted synthesis of unsymmetrical biaryls by Stille cross-coupling reactions." Ultrasonics Sonochemistry 19, no. 3 (May 2012): 410–14. http://dx.doi.org/10.1016/j.ultsonch.2011.08.013.

Full text

APA, Harvard, Vancouver, ISO, and other styles

24

Dien Pham, Phuoc, Jürgen Vitz, Cécile Chamignon, Arnaud Martel, and Stéphanie Legoupy. "Stille Cross-Coupling Reactions with Tin Reagents Supported on Ionic Liquids." European Journal of Organic Chemistry 2009, no. 19 (July 2009): 3249–57. http://dx.doi.org/10.1002/ejoc.200900177.

Full text

APA, Harvard, Vancouver, ISO, and other styles

25

LARHED, M., M. HOSHINO, S. HADIDA, D. P. CURRAN, and A. HALLBERG. "ChemInform Abstract: Rapid Fluorous Stille Coupling Reactions Conducted under Microwave Irradiation." ChemInform 29, no. 2 (June 24, 2010): no. http://dx.doi.org/10.1002/chin.199802076.

Full text

APA, Harvard, Vancouver, ISO, and other styles

26

QUAYLE, P., J. WANG, J. XU, and C. J. URCH. "ChemInform Abstract: Stereoselective Stille Coupling Reactions of 1,1-Bis(trialkylstannyl)ethenes." ChemInform 29, no. 16 (June 23, 2010): no. http://dx.doi.org/10.1002/chin.199816173.

Full text

APA, Harvard, Vancouver, ISO, and other styles

27

Kim, Won-Suk, Hyung-Jin Kim, and Cheon-Gyu Cho. "Regioselectivity in the Stille Coupling Reactions of 3,5-Dibromo-2-pyrone." Journal of the American Chemical Society 125, no. 47 (November 2003): 14288–89. http://dx.doi.org/10.1021/ja037043a.

Full text

APA, Harvard, Vancouver, ISO, and other styles

28

Nehls, B. S., U. Asawapirom, S. Füldner, E. Preis, T. Farrell, and U. Scherf. "Semiconducting Polymers via Microwave-Assisted Suzuki and Stille Cross-Coupling Reactions." Advanced Functional Materials 14, no. 4 (April 2004): 352–56. http://dx.doi.org/10.1002/adfm.200400010.

Full text

APA, Harvard, Vancouver, ISO, and other styles

29

Gribanov, Pavel S., Yulia D. Golenko, Maxim A. Topchiy, Lidiya I. Minaeva, Andrey F. Asachenko, and Mikhail S. Nechaev. "Stannylation of Aryl Halides, Stille Cross-Coupling, and One-Pot, Two-Step Stannylation/Stille Cross-Coupling Reactions under Solvent-Free Conditions." European Journal of Organic Chemistry 2018, no. 1 (January 10, 2018): 120–25. http://dx.doi.org/10.1002/ejoc.201701463.

Full text

APA, Harvard, Vancouver, ISO, and other styles

30

Zhao, Ning, Sunting Xuan, Brandon Byrd, Frank R. Fronczek, Kevin M. Smith, and M. Graça H. Vicente. "Synthesis and regioselective functionalization of perhalogenated BODIPYs." Organic & Biomolecular Chemistry 14, no. 26 (2016): 6184–88. http://dx.doi.org/10.1039/c6ob00935b.

Full text

Abstract:

We report the synthesis of perhalogenated BODIPYs and investigate the regioselective functionalization of a perhalogenated BODIPY using Pd(0)-catalyzed Stille cross-coupling reactions. Further reaction at the boron atom produces nona-functionalized BODIPYs.

APA, Harvard, Vancouver, ISO, and other styles

31

Ma, Xiao, Yajie Chen, Sigui Chen, Zhengshuang Xu, and Tao Ye. "Total syntheses of smenothiazoles A and B." Organic & Biomolecular Chemistry 15, no. 34 (2017): 7196–203. http://dx.doi.org/10.1039/c7ob01818e.

Full text

Abstract:

Stereocontrolled installation of vinyl chloride and the 2,5-diene system via silastannation, Stille reaction and desilylchlorination, and the final peptide coupling reactions led to the concise total synthesis of smenothiazoles A (1) and B (2).

APA, Harvard, Vancouver, ISO, and other styles

32

Anderson, Oren P., Anthony GM Barrett, Jeremy J. Edmunds, Shun-Ichiro Hachiya, James A. Hendrix, Kiyoshi Horita, James W. Malecha, Christopher J. Parkinson, and Andrew VanSickle. "Applications of crotyldiisopinocampheylboranes in synthesis: a formal total synthesis of (+)-calyculin A." Canadian Journal of Chemistry 79, no. 11 (November 1, 2001): 1562–92. http://dx.doi.org/10.1139/v01-133.

Full text

Abstract:

The formal total synthesis of the marine metabolite (+)-calyculin A is reported. The key steps involve (i) the use of Brown allylboration chemistry to control the relative and absolute stereochemistry of homoallylic alcohol arrays, thus setting eight of the desired stereocenters; (ii) Stille coupling methodology in the construction of the cyano tetraene unit of the natural product; and (iii) a modified CornforthMeyers approach to the synthesis of the oxazole fragment.Key words: calyculin, marine natural product, phosphatase inhibitor, total synthesis, palladium catalyzed coupling reactions, allylboration reactions, aldol reactions, spiroketal, CornforthMeyers oxazole reaction.

APA, Harvard, Vancouver, ISO, and other styles

33

Sain, Shalu, Sonika Jain, Manish Srivastava, Rajendra Vishwakarma, and Jaya Dwivedi. "Application of Palladium-Catalyzed Cross-Coupling Reactions in Organic Synthesis." Current Organic Synthesis 16, no. 8 (January 20, 2020): 1105–42. http://dx.doi.org/10.2174/1570179416666191104093533.

Full text

Abstract:

: Palladium-catalyzed cross-coupling reactions have gained a continuously growing interest of synthetic organic chemists. The present review gives a brief account of applications of the palladium-catalyzed cross-coupling reactions in comprehensive synthesis, viz., the Heck, Stille, Suzuki–Miyaura, Negishi, Sonogashira, Buchwald–Hartwig, Ullmann and the Oxidative, decarboxylative cross-coupling reactions, with particular emphasis on the synthesis of heterocyclic compounds.

APA, Harvard, Vancouver, ISO, and other styles

34

Shome, Sanchari, and Surya Prakhash Singh. "Access to small molecule semiconductors via C–H activation for photovoltaic applications." Chemical Communications 54, no. 53 (2018): 7322–25. http://dx.doi.org/10.1039/c8cc02706d.

Full text

APA, Harvard, Vancouver, ISO, and other styles

35

Tessema, Eskedar, Vijayanath Elakkat, Chiao-Fan Chiu, Zong-Lin Tsai, Ka Long Chan, Chia-Rui Shen, Han-Chang Su, and Norman Lu. "Recoverable Palladium-Catalyzed Carbon-Carbon Bond Forming Reactions under Thermomorphic Mode: Stille and Suzuki-Miyaura Reactions." Molecules 26, no. 5 (March 5, 2021): 1414. http://dx.doi.org/10.3390/molecules26051414.

Full text

Abstract:

The reaction of [PdCl2(CH3CN)2] and bis-4,4′-(RfCH2OCH2)-2,2′-bpy (1a–d), where Rf = n-C11F23 (a), n-C10F21 (b), n-C9F19 (c) and n-C8F17 (d), respectively, in the presence of dichloromethane (CH2Cl2) resulted in the synthesis of Pd complex, [PdCl2[4,4′-bis-(RfCH2OCH2)-2,2′-bpy] (2a–d). The Pd-catalyzed Stille arylations of vinyl tributyltin with aryl halides were selected to demonstrate the feasibility of recycling usage with 2a as the catalyst using NMP (N-methyl-2-pyrrolidone) as the solvent at 120–150 °C. Additionally, recycling and electronic effect studies of 2a–c were also carried out for Suzuki-Miyaura reaction of phenylboronic acid derivatives, 4-X-C6H4-B(OH)2, (X = H or Ph) with aryl halide, 4-Y-C6H4-Z, (Y = CN, H or OCH3; Z = I or Br) in dimethylformamide (DMF) at 135–150 °C. At the end of each cycle, the product mixtures were cooled to lower temperature (e.g., −10 °C), and then catalysts were recovered by decantation with Pd leaching less than 1%. The products were quantified by gas chromatography/mass spectrometry (GC/MS) analysis or by the isolated yield. The complex 2a-catalyzed Stille reaction of aryl iodides with vinyl tributyltin have good recycling results for a total of 8 times, with a high yield within short period of time (1–3 h). Similarly, 2a–c-catalyzed Suzuki-Miyaura reactions also have good recycling results. The electronic effect studies from substituents in both Stille and Suzuki-Miyaura coupling reactions showed that electron withdrawing groups speed up the reaction rate. To our knowledge, this is the first example of recoverable fluorous long-chained Pd-catalyzed Stille reactions under the thermomorphic mode.

APA, Harvard, Vancouver, ISO, and other styles

36

Setsune, Jun-ichiro. "Palladium chemistry in recent porphyrin research." Journal of Porphyrins and Phthalocyanines 08, no. 01 (January 2004): 93–102. http://dx.doi.org/10.1142/s1088424604000088.

Full text

Abstract:

Palladium-catalyzed reactions such as Sonogashira coupling, Suzuki coupling, Stille coupling, Heck reactions, and Glaser-Hey oxidation were used to construct porphyrin modules of nano-scale molecular size in recent years. Recent developments in the supramolecular assembly of porphyrins and Pd (II) and in the organopalladium complexes of various porphyrins are also summarized.

APA, Harvard, Vancouver, ISO, and other styles

37

Lee, Victor. "Application of copper(i) salt and fluoride promoted Stille coupling reactions in the synthesis of bioactive molecules." Organic & Biomolecular Chemistry 17, no. 41 (2019): 9095–123. http://dx.doi.org/10.1039/c9ob01602c.

Full text

APA, Harvard, Vancouver, ISO, and other styles

38

Nichele, Tatiana Z., and Adriano L. Monteiro. "Synthesis of diarylmethane derivatives from Stille cross-coupling reactions of benzylic halides." Tetrahedron Letters 48, no. 42 (October 2007): 7472–75. http://dx.doi.org/10.1016/j.tetlet.2007.08.072.

Full text

APA, Harvard, Vancouver, ISO, and other styles

39

Selig, Roland, Dieter Schollmeyer, Wolfgang Albrecht, and Stefan Laufer. "The application of Stille cross-coupling reactions with multiple nitrogen containing heterocycles." Tetrahedron 67, no. 47 (November 2011): 9204–13. http://dx.doi.org/10.1016/j.tet.2011.09.053.

Full text

APA, Harvard, Vancouver, ISO, and other styles

40

Koprowski, Marek, Rosa-Maria Sebastián, Valérie Maraval, Maria Zablocka, Victorio Cadierno, Bruno Donnadieu, Alain Igau, Anne-Marie Caminade, and Jean-Pierre Majoral. "Iminophosphine Palladium Complexes in Catalytic Stille Coupling Reactions: From Monomers to Dendrimers." Organometallics 21, no. 22 (October 2002): 4680–87. http://dx.doi.org/10.1021/om011076m.

Full text

APA, Harvard, Vancouver, ISO, and other styles

41

BETZER, J. F., J. Y. LALLEMAND, and A. PANCRAZI. "ChemInform Abstract: Stille Coupling Reactions in the Preparation of Substituted Trienic Systems." ChemInform 29, no. 30 (June 20, 2010): no. http://dx.doi.org/10.1002/chin.199830269.

Full text

APA, Harvard, Vancouver, ISO, and other styles

42

Strueben, Jan, Paul J. Gates, and Anne Staubitz. "ChemInform Abstract: Tin-Functionalized Azobenzenes as Nucleophiles in Stille Cross-Coupling Reactions." ChemInform 45, no. 31 (July 17, 2014): no. http://dx.doi.org/10.1002/chin.201431196.

Full text

APA, Harvard, Vancouver, ISO, and other styles

43

Skoda-Földes, Rita, György Jeges, László Kollár, Judit Horváth, and Zoltán Tuba. "Synthesis of Pentacyclic Steroids via Tandem Stille Coupling and Diels−Alder Reactions." Journal of Organic Chemistry 62, no. 5 (March 1997): 1326–32. http://dx.doi.org/10.1021/jo9615256.

Full text

APA, Harvard, Vancouver, ISO, and other styles

44

Abboud, Mohamed, Emmanuel Aubert, and Victor Mamane. "Double N-arylation reaction of polyhalogenated 4,4’-bipyridines. Expedious synthesis of functionalized 2,7-diazacarbazoles." Beilstein Journal of Organic Chemistry 8 (February 14, 2012): 253–58. http://dx.doi.org/10.3762/bjoc.8.26.

Full text

Abstract:

Unusual 2,7-diazacarbazoles were prepared in one step from readily available tetra-halogenated 4,4’-bipyridines by using a double N-arylation reaction in the presence of the Pd–XPhos catalyst system. Moderate to good yields were obtained in this site-selective Buchwald–Hartwig double amination. The functionalization of these tricyclic derivatives was performed by using Pd-catalyzed cross-coupling reactions such as the Stille and Suzuki couplings. Two compounds were analyzed by X-ray diffraction and show π–π stacking involving the diazacarbazole moieties and the phenyl rings of functionalized groups.

APA, Harvard, Vancouver, ISO, and other styles

45

Balšánek, Vojtěch, Lucie Tichotová, Jiří Kuneš, Marcel Špulák, Milan Pour, Ivan Votruba, and Vladimír Buchta. "Cytostatic tetrazole–butenolide conjugates: linking tetrazole and butenolide rings via stille coupling and biological activity of the target substances." Collection of Czechoslovak Chemical Communications 74, no. 7-8 (2009): 1161–78. http://dx.doi.org/10.1135/cccc2009040.

Full text

Abstract:

A series of tetrazoles linked to the butenolide core via benzene rings were prepared by the Stille coupling reaction of α-(tributylstannyl)butenolides and 5-(alkylsulfanyl)-1-(4-iodophenyl)tetrazoles, and the compounds were tested for antifungal and cytostatic activity. Interesting antifungal activities against the filamentous strain Absidia corymbifera, and cytostatic activities against leukemic cells HL-60 and CCRF-CEM were found. The cytostatic activity requires the presence of both the butenolide ring and the alkylsulfanyl group bound to tetrazole ring. In addition, the feasibility of Pd-coupling reactions with 5-iodotetrazoles was evaluated.

APA, Harvard, Vancouver, ISO, and other styles

46

Mowery, Molly E., and Philip DeShong. "ChemInform Abstract: Cross-Coupling Reactions of Hypervalent Siloxane Derivatives: An Alternative to Stille and Suzuki Couplings." ChemInform 30, no. 33 (June 14, 2010): no. http://dx.doi.org/10.1002/chin.199933109.

Full text

APA, Harvard, Vancouver, ISO, and other styles

47

Salih, Kifah S. M., and Younis Baqi. "Microwave-Assisted Palladium-Catalyzed Cross-Coupling Reactions: Generation of Carbon–Carbon Bond." Catalysts 10, no. 1 (December 18, 2019): 4. http://dx.doi.org/10.3390/catal10010004.

Full text

Abstract:

Cross-coupling reactions furnishing carbon–carbon (C–C) bond is one of the most challenging tasks in organic syntheses. The early developed reaction protocols by Negishi, Heck, Kumada, Sonogashira, Stille, Suzuki, and Hiyama, utilizing palladium or its salts as catalysis have, for decades, attracted and inspired researchers affiliated with academia and industry. Tremendous efforts have been paid to develop and achieve more sustainable reaction conditions, such as the reduction in energy consumption by applying the microwave irradiation technique. Chemical reactions under controlled microwave conditions dramatically reduce the reaction time and therefore resulting in increase in the yield of the desired product by minimizing the formation of side products. In this review, we mainly focus on the recent advances and applications of palladium catalyzed cross-coupling carbon–carbon bond formation under microwave technology.

APA, Harvard, Vancouver, ISO, and other styles

48

Brimble, Margaret A., and Letecia J. Duncalf. "The Synthesis of Oxygenated Naphthyl Stannanes Possessing ortho-Methoxy Substituents for Use in Stille Coupling Reactions." Australian Journal of Chemistry 52, no. 1 (1999): 19. http://dx.doi.org/10.1071/c98106.

Full text

Abstract:

The preparation of oxygenated naphthyl stannanes bearing an ortho-methoxy substituent is described, including stannanes (23) and (25) which are key intermediates for the synthesis of dimeric pyranonaphthoquinone antibiotics. Stannanes (17), (19) and (21)–(23) were obtained by metal–halogen exchange of the corresponding bromonaphthalenes. In an alternative approach to effect stannylation, a palladium(0)-mediated coupling reaction using hexaalkylditin reagents was examined. The Stille coupling reaction between naphthyl stannanes (23) and (25) and the corresponding bromonaphthalenes (11) and (24) failed to effect coupling to the desired binaphthyls.

APA, Harvard, Vancouver, ISO, and other styles

49

Ghorbani-Choghamarani, Arash, Ali Ashraf Derakhshan, Maryam Hajjami, and Laleh Rajabi. "Copper–Schiff base alumoxane: a new and reusable mesoporous nano catalyst for Suzuki–Miyaura and Stille C–C cross-coupling reactions." RSC Advances 6, no. 97 (2016): 94314–24. http://dx.doi.org/10.1039/c6ra19725f.

Full text

APA, Harvard, Vancouver, ISO, and other styles

50

Lau, Kelvin Chi Yin, and Pauline Chiu. "The application of non-cross-linked polystyrene-supported triphenylarsine in Stille coupling reactions." Tetrahedron Letters 48, no. 10 (March 2007): 1813–16. http://dx.doi.org/10.1016/j.tetlet.2007.01.005.

Full text

APA, Harvard, Vancouver, ISO, and other styles

We offer discounts on all premium plans for authors whose works are included in thematic literature selections. Contact us to get a unique promo code!