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Journal articles on the topic 'Mizoroki-Heck'

Author: Grafiati

Published: 6 July 2022

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1

Srivastava, Vivek. "Synthesis and Characterization of Pd exchanged MMT Clay for Mizoroki-Heck Reaction." Open Chemistry 16, no. 1 (June 20, 2018): 605–13. http://dx.doi.org/10.1515/chem-2018-0065.

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AbstractWe successfully synthesized Pd@MMT clay using a cation exchange process. We characterized all the synthesized Pd@MMT clays using sophisticated analytical techniques before testing them as a heterogeneous catalyst for the Mizoroki - Heck reaction (mono and double). The highest yield of the Mizoroki-Heck reaction product was recovered using thermally stable and highly reactive Pd@ MMT-1 clay catalyst in the functionalized ionic liquid reaction medium. We successfully isolated 2-aryl-vinyl phosphonates (mono-Mizoroki-Heck reaction product) and 2,2-diaryl-vinylphosphonates (double-Mizoroki-Heck reaction product) using aryl halides and dialkyl vinyl phosphonates in higher yields. The low catalyst loading, easy recovery of reaction product and 8 times catalyst recycling are the major highlights of this proposed protocol.

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2

Schmidt, Bernd. "The Mizoroki-Heck Reaction." Synthesis 2010, no. 04 (February 2010): 718. http://dx.doi.org/10.1055/s-0029-1218660.

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3

Watson, Allan, Kirsty Wilson, Jane Murray, Helen Sneddon, and Craig Jamieson. "Dimethylisosorbide (DMI) as a Bio-Derived Solvent for Pd-Catalyzed Cross-Coupling Reactions." Synlett 29, no. 17 (September 28, 2018): 2293–97. http://dx.doi.org/10.1055/s-0037-1611054.

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Palladium-catalyzed bond-forming reactions, such as the Suzuki–Miyaura and Mizoroki–Heck reactions, are some of the most broadly utilized reactions within the chemical industry. These reactions frequently employ hazardous solvents; however, to adhere to increasing sustainability pressures and restrictions regarding the use of such solvents, alternatives are highly sought after. Here we demonstrate the utility of dimethyl isosorbide (DMI) as a bio-derived solvent in several benchmark Pd-catalyzed reactions: Suzuki–Miyaura (13 examples, 62–100% yield), Mizoroki–Heck (13 examples, 47–91% yield), and Sonogashira (12 examples, 65–98% yield).

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4

Ojha, Subhadra, and Niranjan Panda. "Pd-Catalyzed desulfitative arylation of olefins by N-methoxysulfonamide." Organic & Biomolecular Chemistry 20, no. 6 (2022): 1292–98. http://dx.doi.org/10.1039/d1ob02360h.

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5

Yamazaki, Yasuomi, Tatsuki Morimoto, and Osamu Ishitani. "Synthesis of novel photofunctional multinuclear complexes using a coupling reaction." Dalton Transactions 44, no. 25 (2015): 11626–35. http://dx.doi.org/10.1039/c5dt01717c.

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6

Kaur, Navneet, Gurpreet Kaur, Aman Bhalla, Jaspreet S. Dhau, and Ganga Ram Chaudhary. "Metallosurfactant based Pd–Ni alloy nanoparticles as a proficient catalyst in the Mizoroki Heck coupling reaction." Green Chemistry 20, no. 7 (2018): 1506–14. http://dx.doi.org/10.1039/c7gc03877a.

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7

Shibasaki, M., T. Ohshima, and W. Itano. "ChemInform Abstract: Mizoroki-Heck Reaction." ChemInform 42, no. 42 (September 27, 2011): no. http://dx.doi.org/10.1002/chin.201142250.

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8

Wang, Shi-Meng, Hai-Xia Song, Xiao-Yan Wang, Nan Liu, Hua-Li Qin, and Cheng-Pan Zhang. "Palladium-catalyzed Mizoroki–Heck-type reactions of [Ph2SRfn][OTf] with alkenes at room temperature." Chemical Communications 52, no. 80 (2016): 11893–96. http://dx.doi.org/10.1039/c6cc06089g.

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9

Shao, Linjun, and Chenze Qi. "Chitosan microspheres-supported palladium species as an efficient and recyclable catalyst for Mizoroki–Heck reaction." New Journal of Chemistry 41, no. 16 (2017): 8156–65. http://dx.doi.org/10.1039/c7nj01918a.

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10

Zhang, Qing-Song, Shi-Li Wan, Di Chen, Chang-Hua Ding, and Xue-Long Hou. "Palladium-catalyzed asymmetric intermolecular Mizoroki–Heck reaction for construction of a chiral quaternary carbon center." Chemical Communications 51, no. 61 (2015): 12235–38. http://dx.doi.org/10.1039/c5cc03601a.

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11

Landge, Vinod G., Audrey L. Bonds, Thandazile A. Mncwango, Carolina B. Mather, Yasaman Saleh, Hunter L. Fields, Frank Lee, and Michael C. Young. "Amine-directed Mizoroki–Heck arylation of free allylamines." Organic Chemistry Frontiers 9, no. 7 (2022): 1967–74. http://dx.doi.org/10.1039/d2qo00041e.

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12

García, Carolina S., Paula M. Uberman, and Sandra E. Martín. "An effective Pd nanocatalyst in aqueous media: stilbene synthesis by Mizoroki–Heck coupling reaction under microwave irradiation." Beilstein Journal of Organic Chemistry 13 (August 18, 2017): 1717–27. http://dx.doi.org/10.3762/bjoc.13.166.

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Aqueous Mizoroki–Heck coupling reactions under microwave irradiation (MW) were carried out with a colloidal Pd nanocatalyst stabilized with poly(N-vinylpyrrolidone) (PVP). Many stilbenes and novel heterostilbenes were achieved in good to excellent yields starting from aryl bromides and different olefins. The reaction was carried out in a short reaction time and with low catalyst loading, leading to high turnover frequency (TOFs of the order of 100 h−1). The advantages like operational simplicity, high robustness, efficiency and turnover frequency, the utilization of aqueous media and simple product work-up make this protocol a great option for stilbene syntheses by Mizoroki–Heck reaction.

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13

Shen, Chao, Hongyun Shen, Ming Yang, Chengcai Xia, and Pengfei Zhang. "A novel d-glucosamine-derived pyridyl-triazole@palladium catalyst for solvent-free Mizoroki–Heck reactions and its application in the synthesis of Axitinib." Green Chemistry 17, no. 1 (2015): 225–30. http://dx.doi.org/10.1039/c4gc01606h.

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14

Jadhav, Sanjay N., and Chandrashekhar V. Rode. "An efficient palladium catalyzed Mizoroki–Heck cross-coupling in water." Green Chemistry 19, no. 24 (2017): 5958–70. http://dx.doi.org/10.1039/c7gc02869e.

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15

Muthusamy, Gopinathan, and Sunil V. Pansare. "Stereoselective synthesis of E-3-(arylmethylidene)-5-(alkyl/aryl)-2(3H)-furanones by sequential hydroacyloxylation-Mizoroki–Heck reactions of iodoalkynes." Organic & Biomolecular Chemistry 16, no. 42 (2018): 7971–83. http://dx.doi.org/10.1039/c8ob02063a.

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16

Ju, Pengyao, Shujie Wu, Qing Su, Xiaodong Li, Ziqian Liu, Guanghua Li, and Qiaolin Wu. "Salen–porphyrin-based conjugated microporous polymer supported Pd nanoparticles: highly efficient heterogeneous catalysts for aqueous C–C coupling reactions." Journal of Materials Chemistry A 7, no. 6 (2019): 2660–66. http://dx.doi.org/10.1039/c8ta11330k.

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17

Moitra, Nirmalya, Ayumi Matsushima, Toshiyuki Kamei, Kazuyoshi Kanamori, Yumi H. Ikuhara, Xiang Gao, Kazuyuki Takeda, Yang Zhu, Kazuki Nakanishi, and Toyoshi Shimada. "A new hierarchically porous Pd@HSQ monolithic catalyst for Mizoroki–Heck cross-coupling reactions." New J. Chem. 38, no. 3 (2014): 1144–49. http://dx.doi.org/10.1039/c3nj01433a.

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18

Puthiaraj, Pillaiyar, and Kasi Pitchumani. "Palladium nanoparticles supported on triazine functionalised mesoporous covalent organic polymers as efficient catalysts for Mizoroki–Heck cross coupling reaction." Green Chem. 16, no. 9 (2014): 4223–33. http://dx.doi.org/10.1039/c4gc00412d.

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19

Martín, Laura, Elies Molins, and Adelina Vallribera. "Tuning and enhancement of the Mizoroki–Heck reaction using polarized Pd nanocomposite carbon aerogels." New Journal of Chemistry 40, no. 12 (2016): 10208–12. http://dx.doi.org/10.1039/c6nj02279k.

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20

Martínez, Alejandro V., Alejandro Leal-Duaso, José I. García, and José A. Mayoral. "An extremely highly recoverable clay-supported Pd nanoparticle catalyst for solvent-free Heck–Mizoroki reactions." RSC Advances 5, no. 74 (2015): 59983–90. http://dx.doi.org/10.1039/c5ra10191c.

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21

Putta, Chandrababu, Vittal Sharavath, Suprabhat Sarkar, and Sutapa Ghosh. "Palladium nanoparticles on β-cyclodextrin functionalised graphene nanosheets: a supramolecular based heterogeneous catalyst for C–C coupling reactions under green reaction conditions." RSC Advances 5, no. 9 (2015): 6652–60. http://dx.doi.org/10.1039/c4ra14323j.

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Palladium nanoparticles on β-cyclodextrin functionalised graphene based supramolecular heterogeneous catalyst are used for Suzuki–Miyaura and Heck–Mizoroki coupling reactions under green reaction conditions.

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22

Nejat, Razieh, Ali Reza Mahjoub, Zahra Hekmatian, and Tahereh Azadbakht. "Pd-functionalized MCM-41 nanoporous silica as an efficient and reusable catalyst for promoting organic reactions." RSC Advances 5, no. 21 (2015): 16029–35. http://dx.doi.org/10.1039/c4ra11850b.

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23

Mandegani, Zeinab, Mozaffar Asadi, Zahra Asadi, Afshan Mohajeri, Nasser Iranpoor, and Akbar Omidvar. "A nano tetraimine Pd(0) complex: synthesis, characterization, computational studies and catalytic applications in the Heck–Mizoroki reaction in water." Green Chemistry 17, no. 6 (2015): 3326–37. http://dx.doi.org/10.1039/c5gc00616c.

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24

Takata, Shohei, Yuta Endo, Mohammad Shahid Ullah, and Shinichi Itsuno. "Synthesis of cinchona alkaloid sulfonamide polymers as sustainable catalysts for the enantioselective desymmetrization of cyclic anhydrides." RSC Advances 6, no. 76 (2016): 72300–72305. http://dx.doi.org/10.1039/c6ra14535c.

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Mizoroki–Heck polymerization of cinchona sulfonamide gave chiral polymers, which are active catalysts for enantioselective desymmetrization of cyclic anhydrides to give chiral hemiesters in high yield with high enantioselectivities.

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25

Rouzifar, Majid, Sara Sobhani, Alireza Farrokhi, and José Miguel Sansano. "Fe-MIL-101 modified by isatin-Schiff-base-Co: a heterogeneous catalyst for C–C, C–O, C–N, and C–P cross coupling reactions." New Journal of Chemistry 45, no. 42 (2021): 19963–76. http://dx.doi.org/10.1039/d1nj03468e.

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26

Garnes-Portolés, Francisco, Rossella Greco, Judit Oliver-Meseguer, Jorge Castellanos-Soriano, M. Consuelo Jiménez, Miguel López-Haro, Juan Carlos Hernández-Garrido, Mercedes Boronat, Raúl Pérez-Ruiz, and Antonio Leyva-Pérez. "Regioirregular and catalytic Mizoroki–Heck reactions." Nature Catalysis 4, no. 4 (April 2021): 293–303. http://dx.doi.org/10.1038/s41929-021-00592-3.

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27

Sharavath, Vittal, and Sutapa Ghosh. "Palladium nanoparticles on noncovalently functionalized graphene-based heterogeneous catalyst for the Suzuki–Miyaura and Heck–Mizoroki reactions in water." RSC Adv. 4, no. 89 (2014): 48322–30. http://dx.doi.org/10.1039/c4ra06868h.

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Palladium nanoparticles supported on noncovalently functionalized graphene based heterogeneous catalyst for the Suzuki–Miyaura and Heck–Mizoroki C–C coupling reactions towards aryl bromides and less reactive aryl chlorides in water.

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28

Matsheku, Asanda C., Richard Tia, Munaka C. Maumela, and Banothile C. E. Makhubela. "Ferrocenylimine Palladium (II) Complexes: Synthesis, Characterization and Application in Mizoroki-Heck and Suzuki-Miyaura Cross-Coupling Reactions." Catalysts 11, no. 7 (June 22, 2021): 755. http://dx.doi.org/10.3390/catal11070755.

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Carbon-carbon cross-coupling reactions are essential synthetic tools for synthesizing polymers, natural products, agrochemicals, and pharmaceuticals. Therefore, new catalysts that function with greater efficiency and functional group tolerance are being researched. We have prepared new ferrocenylimine monodentate N and P donor ligands and N^N and N^P bidentate chelating ligands (L1 to L4) employed in stabilizing palladium ions for application in Mizoroki-Heck and Suzuki-Miyaura cross-coupling reactions. The ferrocenylimine ligands were successfully synthesized by Schiff base condensation reactions of acetyl ferrocene with hydrazine monohydrate to afford ferrocenyl hydrazone (L1). Ligand L1 was further treated with aldehydes to give ferrocenyl(2-diphenylphosphino)imine (L3) and ferrocenyl(pyridyl)imine (L3), while phosphination of L1 with chlorodiphenylphosphine afforded L2. The ligands were used to prepare new palladium(II) complexes (C1 to C4) by complexation with [PdCl2(MeCN)2]. All the ligands and complexes were fully characterized using standard spectroscopic and analytical techniques, including 1H NMR and 13C NMR spectroscopy, FT-IR spectroscopy, mass spectrometry and elemental analysis. The complexes (C1 to C4) were tested for efficacies in catalyzing Mizoroki-Heck and Suzuki-Miyaura C-C cross-coupling reactions and proved to be suitable catalyst precursors. Ferrocenyl(2-diphenylphosphine)imino and ferrocenyl-methyl hydrazone palladium(II) complexes C2 and C3 showed the best activities at TONs of up to 201. The ferrocenyl palladium(II) (pre)catalysts demonstrated moderate activity in Mizoroki-Heck reactions involving substrates with substituents on the olefin and aryl halide (including 4-Cl, 4-CH3, -CO2Me and -CO2Et). Density Functional Theory was used to study the mechanism of the Mizoroki-Heck cross-coupling reactions and have led to confirmation of the widely accepted catalytic cycle. Catalyst precursors (C1 to C4) also displayed good activity and selectivity in Suzuki-Miyaura cross-coupling reactions, at 0.5 mol% catalyst loading, with good tolerance to functional groups present on the aryl halide and boronic acid substrates (such as 4-Cl, 4-CHO, 4-COOH, 3-NO2, 3,5-dimethoxy and 4-CH3).

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29

Lee, Jhen-Yi, Jiun-Shian Shen, Ru-Jiun Tzeng, I.-Chen Lu, Jenn-Huei Lii, Ching-Han Hu, and Hon Man Lee. "Well-defined palladium(0) complexes bearing N-heterocyclic carbene and phosphine moieties: efficient catalytic applications in the Mizoroki–Heck reaction and direct C–H functionalization." Dalton Transactions 45, no. 25 (2016): 10375–88. http://dx.doi.org/10.1039/c6dt01323f.

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A well-defined palladium(0) complex with a phosphine-functionalized N-heterocyclic carbene ligand was prepared and shown to be inefficient in catalyzing Mizoroki–Heck coupling and direct C–H functionalization reactions.

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30

Rangraz, Yalda, Firouzeh Nemati, and Ali Elhampour. "Organoselenium–palladium(ii) complex immobilized on functionalized magnetic nanoparticles as a promising retrievable nanocatalyst for the “phosphine-free” Heck–Mizoroki coupling reaction." New Journal of Chemistry 42, no. 18 (2018): 15361–71. http://dx.doi.org/10.1039/c8nj02433b.

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An air- and moisture-stable organoselenium–palladium complex immobilized on silica-coated magnetic nanoparticles is designed, synthesized and applied as a practical and retrievable catalyst in the Heck–Mizoroki cross-coupling reaction.

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31

Khamrai, Jagadish, Saikat Das, Aleksandr Savateev, Markus Antonietti, and Burkhard König. "Mizoroki–Heck type reactions and synthesis of 1,4-dicarbonyl compounds by heterogeneous organic semiconductor photocatalysis." Green Chemistry 23, no. 5 (2021): 2017–24. http://dx.doi.org/10.1039/d0gc03792c.

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We report the synthesis of 1,4-dicarbonyl compounds and substituted alkenes (Mizoroki–Heck type coupling) starting from secondary and tertiary alkyl halides and vinyl acetate or styrene derivatives using visible-light photocatalysis.

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32

Pradhan, Subhashis, and Rohith P. John. "A discrete self-assembled palladium nano-cage catalyses Suzuki–Miyaura coupling heterogeneously and Heck–Mizoroki coupling homogeneously." New Journal of Chemistry 39, no. 7 (2015): 5759–66. http://dx.doi.org/10.1039/c5nj01032b.

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A coordination driven Pd₂L₄ nano-cage heterogeneously catalysed Suzuki–Miyaura coupling and homogeneously catalysed Heck–Mizoroki coupling under aerobic phosphine free conditions without significant loss of activity.

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33

Martínez, Alejandro V., Fabio Invernizzi, Alejandro Leal-Duaso, José A. Mayoral, and José I. García. "Microwave-promoted solventless Mizoroki–Heck reactions catalysed by Pd nanoparticles supported on laponite clay." RSC Advances 5, no. 14 (2015): 10102–9. http://dx.doi.org/10.1039/c4ra15418e.

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Palladium nanoparticles supported on laponite efficiently catalyse solventless Mizoroki–Heck reactions activated by microwaves. High yields are obtained in a few minutes and the catalyst can be efficiently recovered and reused up to thirteen times.

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34

Madden, Katrina S., Sylvain David, Jonathan P. Knowles, and Andrew Whiting. "Heck–Mizoroki coupling of vinyliodide and applications in the synthesis of dienes and trienes." Chemical Communications 51, no. 57 (2015): 11409–12. http://dx.doi.org/10.1039/c5cc03273c.

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Vinyliodide reacts chemoselectively under Heck–Mizoroki conditions with terminal alkenes to give diene products, including vinyl boronate esters, and the resulting dienylboronate undergoes Suzuki–Miyaura coupling with aryl, heteroaryl and alkenyl halides to access dienes and trienes.

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35

Yamazaki, Yasuomi, and Osamu Ishitani. "Selectivity control between Mizoroki–Heck and homo-coupling reactions for synthesising multinuclear metal complexes: unique addition effects of tertiary phosphines and O2." Dalton Transactions 46, no. 14 (2017): 4816–23. http://dx.doi.org/10.1039/c7dt00922d.

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Selectivity control between the Mizoroki–Heck and the homo-coupling reactions for synthesising multinuclear metal complexes could be achieved by using tertiary phosphines and air, which affected the particle size of Pd species as catalysts for the reactions.

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36

Yuen, On Ying, Chau Ming So, and Fuk Yee Kwong. "Open-air oxidative Mizoroki–Heck reaction of arylsulfonyl hydrazides with alkenes." RSC Advances 6, no. 33 (2016): 27584–89. http://dx.doi.org/10.1039/c6ra03188a.

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A palladium(ii)-catalyzed oxidative Mizoroki–Heck reaction of arylsulfonyl hydrazides with alkenes was developed employing Pd(OAc)₂ and pyridine ligand L9 as a catalyst system and atmospheric air as the sole oxidant in an open-vessel manner.

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37

Ghosh, Koena, Shubhajit Dhara, Sourav Jana, Subhomoy Das, and Sudeshna Roy. "NHC stabilized Pd nanoclusters in the Mizoroki–Heck reaction within microemulsion: exploring the role of imidazolium salt in rate enhancement." New Journal of Chemistry 43, no. 4 (2019): 1993–2001. http://dx.doi.org/10.1039/c8nj05118f.

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Significant rate enhancement of the Mizoroki–Heck reaction by in situ generated palladium nanoclusters within the confined space of water-in-oil mixed microemulsion in the presence of novel imidazo[1,5-α]pyridinium chlorides as N-heterocyclic carbene (NHC) precursors is reported.

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38

Santos, Carla I. M., Joana F. B. Barata, M. Amparo F. Faustino, Carlos Lodeiro, and M. Graça P. M. S. Neves. "Revisiting Heck–Mizoroki reactions in ionic liquids." RSC Advances 3, no. 42 (2013): 19219. http://dx.doi.org/10.1039/c3ra43493a.

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39

Schmidt, Bernd, Frank Hölter, René Berger, and Sönke Jessel. "Mizoroki-Heck Reactions with 4-Phenoldiazonium Salts." Advanced Synthesis & Catalysis 352, no. 14-15 (September 23, 2010): 2463–73. http://dx.doi.org/10.1002/adsc.201000493.

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40

SRIVASTAVA, VIVEK. "Carbene Based Palladium-catalyzed Mizoroki-Heck Reaction." Oriental Journal Of Chemistry 28, no. 4 (December 22, 2012): 1859–63. http://dx.doi.org/10.13005/ojc/280444.

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41

Han, Xiao-Qing, Lei Wang, Ping Yang, Jing-Yuan Liu, Wei-Yan Xu, Chao Zheng, Ren-Xiao Liang, Shu-Li You, Junliang Zhang, and Yi-Xia Jia. "Enantioselective Dearomative Mizoroki–Heck Reaction of Naphthalenes." ACS Catalysis 12, no. 1 (December 23, 2021): 655–61. http://dx.doi.org/10.1021/acscatal.1c05008.

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42

Jouffroy, Matthieu, Rafael Gramage-Doria, David Sémeril, Dominique Armspach, Dominique Matt, Werner Oberhauser, and Loïc Toupet. "Phosphinocyclodextrins as confining units for catalytic metal centres. Applications to carbon–carbon bond forming reactions." Beilstein Journal of Organic Chemistry 10 (October 15, 2014): 2388–405. http://dx.doi.org/10.3762/bjoc.10.249.

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The capacity of two cavity-shaped ligands, HUGPHOS-1 and HUGPHOS-2, to generate exclusively singly phosphorus-ligated complexes, in which the cyclodextrin cavity tightly wraps around the metal centre, was explored with a number of late transition metal cations. Both cyclodextrin-derived ligands were assessed in palladium-catalysed Mizoroki–Heck coupling reactions between aryl bromides and styrene on one hand, and the rhodium-catalysed asymmetric hydroformylation of styrene on the other hand. The inability of both chiral ligands to form standard bis(phosphine) complexes under catalytic conditions was established by high-pressure NMR studies and shown to have a deep impact on the two carbon–carbon bond forming reactions both in terms of activity and selectivity. For example, when used as ligands in the rhodium-catalysed hydroformylation of styrene, they lead to both high isoselectivity and high enantioselectivity. In the study dealing with the Mizoroki–Heck reactions, comparative tests were carried out with WIDEPHOS, a diphosphine analogue of HUGPHOS-2.

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43

Sharma, Kamal Nayan, Naveen Satrawala, Avinash Kumar Srivastava, Munsaf Ali, and Raj Kumar Joshi. "Palladium(ii) ligated with a selenated (Se, CNHC, N−)-type pincer ligand: an efficient catalyst for Mizoroki–Heck and Suzuki–Miyaura coupling in water." Organic & Biomolecular Chemistry 17, no. 40 (2019): 8969–76. http://dx.doi.org/10.1039/c9ob01674k.

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First Pd(ii) complex of a novel (Se, C_NHC, N⁻) type pincer ligand based on selenated NHC was synthesized and found to be very efficient in the catalysis of Mizoroki–Heck coupling of ArCl/Br and Suzuki–Miyaura coupling of ArBr in water.

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44

Kusy, Damian, Agata Wojciechowska, Joanna Małolepsza, and Katarzyna M. Błażewska. "Functionalization of the imidazo[1,2-a]pyridine ring in α-phosphonoacrylates and α-phosphonopropionates via microwave-assisted Mizoroki–Heck reaction." Beilstein Journal of Organic Chemistry 16 (January 3, 2020): 15–21. http://dx.doi.org/10.3762/bjoc.16.3.

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A series of new phosphonocarboxylates containing an imidazo[1,2-a]pyridine ring has been synthesized via the microwave-assisted Mizoroki–Heck reaction. The efficient modification of the imidazo[1,2-a]pyridine ring has been achieved as late-stage functionalization, enabling and accelerating the generation of a library of compounds from a common precursor.

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45

Csuk, René, and Sabrina Albert. "A Short Synthesis of Rhaponticin and its 3”-Fluoroanalog via a Wittig/Heck-Mizoroki Route." Zeitschrift für Naturforschung B 66, no. 3 (March 1, 2011): 311–16. http://dx.doi.org/10.1515/znb-2011-0314.

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Rhaponticin and its 3”-fluoroanalog have been prepared from easily accessible starting materials. The key step of these syntheses is the silver carbonate-mediated glycosidation reaction employed for the selective formation of a β -glycosidic bond. A palladium acetate-catalyzed Heck-Mizoroki reaction in triethanolamine established an (E) configuration in the stilbene with simultaneous deprotection of the carbohydrate.

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46

Usami, Yoshihide, Hayato Ichikawa, and Shinya Harusawa. "Heck-Mizoroki Reaction of 4-Iodo-1H-pyrazoles." HETEROCYCLES 83, no. 4 (2011): 827. http://dx.doi.org/10.3987/com-11-12146.

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47

Berteina-Raboin, Sabine. "Catalyzed Mizoroki-Heck Reaction or C-H Activation." Catalysts 9, no. 11 (November 6, 2019): 925. http://dx.doi.org/10.3390/catal9110925.

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In the last few decade, research conducted on the development by catalytic processes of C-C bonds formation on the one hand and on the other hand on the activation of C-H bonds has grown considerably [...]

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48

Suganthy, Pandimuni Kalpaga, Rupesh Narayana Prabhu, and Venugopal Shamugham Sridevi. "Nickel(II) thiosemicarbazone complex catalyzed Mizoroki–Heck reaction." Tetrahedron Letters 54, no. 42 (October 2013): 5695–98. http://dx.doi.org/10.1016/j.tetlet.2013.08.018.

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Walker, Benjamin R., and Christo S. Sevov. "An Electrochemically Promoted, Nickel-Catalyzed Mizoroki–Heck Reaction." ACS Catalysis 9, no. 8 (July 2019): 7197–203. http://dx.doi.org/10.1021/acscatal.9b02230.

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Uno, Daisuke, Hiroko Minami, Shinya Otsuka, Keisuke Nogi, and Hideki Yorimitsu. "Palladium-Catalyzed Mizoroki-Heck-Type Alkenylation of Monoaryldialkylsulfoniums." Chemistry - An Asian Journal 13, no. 17 (June 10, 2018): 2397–400. http://dx.doi.org/10.1002/asia.201800489.

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