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Journal articles on the topic 'One-pot catalysis'

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Published: 7 July 2024
Last updated: 7 July 2024

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1

Choi, Youngbo, Yang Sik Yun, Hongseok Park, Dae Sung Park, Danim Yun, and Jongheop Yi. "A facile approach for the preparation of tunable acid nano-catalysts with a hierarchically mesoporous structure." Chem. Commun. 50, no. 57 (2014): 7652–55. http://dx.doi.org/10.1039/c4cc01881h.

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2

Kumar, Devarapalli Ravi, and Gedu Satyanarayana. "Palladium Catalysis: One‐Pot Synthesis of Fluorenones." ChemistrySelect 3, no. 27 (July 18, 2018): 7867–70. http://dx.doi.org/10.1002/slct.201801787.

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3

Zhang, Luxin, Xu Xing, Ruijun Sun, and Meng Hu. "Catalytic conversion of carbohydrates into 5-ethoxymethylfurfural using γ-AlOOH and CeO2@B2O3 catalyst synergistic effect." RSC Advances 12, no. 36 (2022): 23118–28. http://dx.doi.org/10.1039/d2ra01866g.

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4

Sau, Samaresh Chandra, Sudipta Raha Roy, and Swadhin K. Mandal. "One-Pot Consecutive Catalysis by Integrating Organometallic Catalysis with Organocatalysis." Chemistry - An Asian Journal 9, no. 10 (August 14, 2014): 2806–13. http://dx.doi.org/10.1002/asia.201402363.

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5

Pellissier, Hélène. "Asymmetric Zinc Catalysis in Green One-pot Processes." Current Organic Chemistry 25, no. 8 (April 28, 2021): 857–75. http://dx.doi.org/10.2174/1385272825666210216123607.

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This review collects for the first time enantioselective one-pot processes promoted by green chiral zinc catalysts. It illustrates how much these cheap, non-toxic and environmentally benign catalysts allow unprecedented asymmetric domino and tandem reactions of many types to be achieved, allowing direct access to a wide variety of very complex chiral molecules.
6

De Nisi, A., S. Sierra, M. Ferrara, M. Monari, and M. Bandini. "TBAF catalyzed one-pot synthesis of allenyl-indoles." Organic Chemistry Frontiers 4, no. 9 (2017): 1849–53. http://dx.doi.org/10.1039/c7qo00414a.

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7

Prochazka, Michal P., Rolf Carlson, Pentti Mälkönen, Heikki Hukkanen, M. Nielsen, M. S. Lehmann, and Tadashi Tokii. "One-Pot Fischer Indole Synthesis by Zeolite Catalysis." Acta Chemica Scandinavica 44 (1990): 614–16. http://dx.doi.org/10.3891/acta.chem.scand.44-0614.

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8

Gao, Xiang, and Henri B. Kagan. "One-pot multi-substrate screening in asymmetric catalysis." Chirality 10, no. 1-2 (1998): 120–24. http://dx.doi.org/10.1002/chir.19.

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9

Gao, Xiang, and Henri B. Kagan. "One‐pot multi‐substrate screening in asymmetric catalysis." Chirality 10, no. 12 (1998): 120–24. http://dx.doi.org/10.1002/(sici)1520-636x(1998)10:1/2<120::aid-chir19>3.3.co;2-1.

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10

Hou, Fang, Wei Zheng, and Nasser Yousefi. "Design, Characterization and Application of The SCMNPs@PC/VB1-Zn as A Green and Recyclable Biocatalyst for Synthesis of Pyrano[2,3-c]pyrazole and 4H-benzo-[b]-pyran Derivatives." Bulletin of Chemical Reaction Engineering & Catalysis 15, no. 1 (January 3, 2020): 199–212. http://dx.doi.org/10.9767/bcrec.15.1.6179.199-212.

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Eco-friendly and reusable solid acid catalysts (SCMNPs@PC/VB1-Zn) were identified as one of the most effective basic catalysts for the composition of a pot, three-component pyrano[2,3-c]pyrazoles. Methyl-1-phenyl-1H-pyrazole-5(4H)-one, benzaldehyde and malononitrile in high yield at 80 °C. SCMNPs@ PC/VB1-Zn reports the simple and efficient catalysis of a three-component pot reaction of dimedone, aldehydes, and malononitrile to 4H-benzo-[b]-pyran derivatives. This magnetic nanocatalyst can be recycled more than 6 times without dramatically reducing performance with respect to reaction time and efficiency. Copyright © 2020 BCREC Group. All rights reserved
11

Faul, Dieter, Edith Leber, and Gerhard Himbert. "One-Pot Synthesis of Hexatriynediamines." Synthesis 1987, no. 01 (1987): 73–74. http://dx.doi.org/10.1055/s-1987-27853.

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12

Niu, Chengrong, Jie Hu, Yinfeng Li, Jinghang Leng, and Songjun Li. "A thermoresponsive nanorattle containing two different catalysts for controllable one-pot tandem catalysis." Nanotechnology 29, no. 10 (January 30, 2018): 105501. http://dx.doi.org/10.1088/1361-6528/aaa3d2.

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13

Tang, Xinxin, Lan Gan, Xin Zhang, and Zheng Huang. "n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis." Science Advances 6, no. 47 (November 2020): eabc6688. http://dx.doi.org/10.1126/sciadv.abc6688.

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Nature is able to synergistically combine multiple enzymes to conduct well-ordered biosynthetic transformations. Mimicking nature’s multicatalysis in vitro may give rise to new chemical transformations via interplay of numerous molecular catalysts in one pot. The direct and selective conversion of abundant n-alkanes to valuable n-alcohols is a reaction with enormous potential applicability but has remained an unreached goal. Here, we show that a quadruple relay catalysis system involving three discrete transition metal catalysts enables selective synthesis of n-alcohols via n-alkane primary C─H bond hydroxymethylation. This one-pot multicatalysis system is composed of Ir-catalyzed alkane dehydrogenation, Rh-catalyzed olefin isomerization and hydroformylation, and Ru-catalyzed aldehyde hydrogenation. This system is further applied to synthesis of α,ω-diols from simple α-olefins through terminal-selective hydroxymethylation of silyl alkanes.
14

Corma, Avelino, Javier Navas, and Maria J. Sabater. "Advances in One-Pot Synthesis through Borrowing Hydrogen Catalysis." Chemical Reviews 118, no. 4 (January 10, 2018): 1410–59. http://dx.doi.org/10.1021/acs.chemrev.7b00340.

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15

Ballini, Roberto, Giovanna Bosica, Dennis Fiorini, and Alessandro Palmieri. "One-Pot Synthesis of 1,3-Dinitroalkanes under Heterogeneous Catalysis." Synthesis 2004, no. 12 (July 21, 2004): 1938–40. http://dx.doi.org/10.1055/s-2004-829160.

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16

Hashmi, A. Stephen K., and Anna Littmann. "Gold Catalysis: One-Pot Alkylideneoxazoline Synthesis/Alder-Ene Reaction." Chemistry - An Asian Journal 7, no. 6 (March 20, 2012): 1435–42. http://dx.doi.org/10.1002/asia.201200046.

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17

Xiao, Xiong, Jing Zeng, Jing Fang, Jiuchang Sun, Ting Li, Zejin Song, Lei Cai, and Qian Wan. "One-Pot Relay Glycosylation." Journal of the American Chemical Society 142, no. 12 (March 9, 2020): 5498–503. http://dx.doi.org/10.1021/jacs.0c00447.

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18

Parenty, Alexis, and Leroy Cronin. "One-Pot Synthesis of Imidazopyridine Derivatives." Synthesis 2008, no. 9 (May 2008): 1479–85. http://dx.doi.org/10.1055/s-2007-1000936.

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19

Bayarmagnai, Bilguun, Christian Matheis, Eugen Risto, and Lukas J. Goossen. "One-Pot Sandmeyer Trifluoromethylation and Trifluoromethylthiolation." Advanced Synthesis & Catalysis 356, no. 10 (June 20, 2014): 2343–48. http://dx.doi.org/10.1002/adsc.201400340.

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20

Shu, Fan, Qingjuan Zheng, Wanrong Dong, Zhihong Peng, and Delie An. "One-pot synthesis of propynoates and propynenitriles." Canadian Journal of Chemistry 95, no. 2 (February 2017): 144–48. http://dx.doi.org/10.1139/cjc-2016-0181.

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An efficient transformation towards propynoates and propynenitriles is herein described. The practical methodology was conducted at low temperature (–78 or –60 °C) in a one-pot manner with the assistance of base rather than any transition metal catalysts. The base-induced protocol exhibits good functional group tolerance (up to 28 examples) and high efficiency (up to 92% yields) towards substituted acetylenes of great synthetic significance, which was also well demonstrated by the gram-scale reactions.
21

Pirouz, Maryam, M. Saeed Abaee, Pernille Harris, and Mohammad M. Mojtahedi. "One-pot synthesis of benzofurans via heteroannulation of benzoquinones." Heterocyclic Communications 27, no. 1 (January 1, 2021): 24–31. http://dx.doi.org/10.1515/hc-2020-0120.

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Abstract Three different reactions were explored leading to the synthesis of various benzofurans. All reactions took place under AcOH catalysis in a one-pot manner. As a result, benzoquinone derivatives underwent heteroannulation with either itself or cyclohexanones to produce furanylidene-benzofuran or benzofuran structures, respectively.
22

Luan, Huimin, Chi Lei, Qinming Wu, Na Sheng, Yeqing Wang, Xiangju Meng, and Feng-Shou Xiao. "Sustainable one-pot preparation of fully crystalline shaped zeolite catalysts." Catalysis Science & Technology 11, no. 16 (2021): 5650–55. http://dx.doi.org/10.1039/d1cy00948f.

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23

Szőllősi, György. "Asymmetric one-pot reactions using heterogeneous chemical catalysis: recent steps towards sustainable processes." Catalysis Science & Technology 8, no. 2 (2018): 389–422. http://dx.doi.org/10.1039/c7cy01671a.

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24

Cao, Yueling, Hepeng Zhang, Kangkai Liu, and Kai-Jie Chen. "Water-assisted one-pot synthesis of N-doped carbon supported Ru catalysts for heterogeneous catalysis." Chemical Communications 56, no. 76 (2020): 11311–14. http://dx.doi.org/10.1039/d0cc04743k.

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25

Chatterjee, Basujit, Deepti Kalsi, Akash Kaithal, Alexis Bordet, Walter Leitner, and Chidambaram Gunanathan. "One-pot dual catalysis for the hydrogenation of heteroarenes and arenes." Catalysis Science & Technology 10, no. 15 (2020): 5163–70. http://dx.doi.org/10.1039/d0cy00928h.

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A catalytic system resulting from a monohydrido bridged ruthenium complex hydrogenated both heteroarenes and arenes, exhibited dual catalysis and provided access to valuable saturated heterocycles and cycloalkanes.
26

Zhao, Xinpeng, Wang Liu, Lijun Zhu, Yanfei Zhang, Mengya Sun, Gai Miao, Hu Luo, Shenggang Li, and Lingzhao Kong. "Efficient one-pot tandem catalysis of glucose into 1,1,2-trimethoxyethane over W-Beta catalysts." Sustainable Energy & Fuels 6, no. 4 (2022): 1051–57. http://dx.doi.org/10.1039/d1se02048j.

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27

Motokura, Ken. "Development of Multiactive Site Catalysts for Surface Concerted Catalysis Aimed at One-Pot Synthesis." Bulletin of the Chemical Society of Japan 90, no. 2 (February 15, 2017): 137–47. http://dx.doi.org/10.1246/bcsj.20160291.

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28

Ren, Yufeng, Wei Zhang, Jun Lu, Kai Gao, Xiali Liao, and Xiaozhen Chen. "One-pot synthesis of tetrahydro-4H-chromenes by supramolecular catalysis in water." RSC Advances 5, no. 97 (2015): 79405–12. http://dx.doi.org/10.1039/c5ra14385c.

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29

Davies, Alyn T., John M. Curto, Scott W. Bagley, and Michael C. Willis. "One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides." Chemical Science 8, no. 2 (2017): 1233–37. http://dx.doi.org/10.1039/c6sc03924c.

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30

Cui, Hai-Lei, and Fujie Tanaka. "One-pot synthesis of polysubstituted 3-acylpyrroles by cooperative catalysis." Org. Biomol. Chem. 12, no. 31 (2014): 5822–26. http://dx.doi.org/10.1039/c4ob01019a.

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Polysubstituted 3-acylpyrroles were synthesized from readily available unsaturated ketones and N-substituted propargylated amines via an aza-Michael/alkyne carbocyclization cascade followed by oxidation in one pot.
31

Li, Yong-Qi, Peng Wang, Huan Liu, Yong Lu, Xiao-Li Zhao, and Ye Liu. "Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins." Green Chemistry 18, no. 6 (2016): 1798–806. http://dx.doi.org/10.1039/c5gc02127h.

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32

Rene, Loic, Joël Poncet, and Gilles Auzou. "A One Pot Synthesis of β-Cyanoenamines." Synthesis 1986, no. 05 (1986): 419–20. http://dx.doi.org/10.1055/s-1986-31661.

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33

El Cherif, Souheir, and Loïc René. "A One-Pot Synthesis of β-Acylenamines." Synthesis 1988, no. 02 (1988): 138–40. http://dx.doi.org/10.1055/s-1988-27492.

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34

Dehmlow, E. V., U. Fastabend, and M. Keßler. "A One-Pot Synthesis of Trimethylsilyl Fluoride." Synthesis 1988, no. 12 (1988): 996–97. http://dx.doi.org/10.1055/s-1988-27783.

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35

Hudson, Richard, David Fouchard, and L. Tillekeratne. "An Efficient One-Pot Synthesis of Aminobenzimidazoles." Synthesis 2005, no. 01 (November 17, 2004): 17–18. http://dx.doi.org/10.1055/s-2004-834925.

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36

Handy, Scott, and Samantha Anderson. "One-Pot Double Suzuki Couplings of Dichloropyrimidines." Synthesis 2010, no. 16 (July 7, 2010): 2721–24. http://dx.doi.org/10.1055/s-0030-1258150.

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37

Schmalz, Hans-Günther, and Peter Huy. "Practical One-Pot Double Functionalizations of Proline." Synthesis 2011, no. 06 (February 10, 2011): 954–60. http://dx.doi.org/10.1055/s-0030-1258428.

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38

Korpak, Margarete, and Jörg Pietruszka. "Chemoenzymatic One-Pot Synthesis of γ-Butyrolactones." Advanced Synthesis & Catalysis 353, no. 9 (June 2011): 1420–24. http://dx.doi.org/10.1002/adsc.201100110.

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39

Peterson, Geneva R, and Nick Bampos. "One-Pot Synthesis of Indene-Expanded Porphyrins." Angewandte Chemie International Edition 49, no. 23 (May 10, 2010): 3930–33. http://dx.doi.org/10.1002/anie.200906580.

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40

Matsumoto, Kazuhiro, Yuki Oba, Yumiko Nakajima, Shigeru Shimada, and Kazuhiko Sato. "One-Pot Sequence-Controlled Synthesis of Oligosiloxanes." Angewandte Chemie International Edition 57, no. 17 (March 15, 2018): 4637–41. http://dx.doi.org/10.1002/anie.201801031.

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41

Inamdar, Suleman M., Ashok Konala, and Nitin T. Patil. "When gold meets chiral Brønsted acid catalysts: extending the boundaries of enantioselective gold catalysis." Chem. Commun. 50, no. 96 (2014): 15124–35. http://dx.doi.org/10.1039/c4cc04633a.

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This review describes the development in the use of Au(i)/Brønsted acid binary catalytic systems to enable an enantioselective transformation in one-pot that cannot be achieved by gold catalysts alone.
42

Mo, Hanjie, Chengmin Pan, Dingben Chen, Di Chen, Jianrong Gao, and Jianguo Yang. "Phosphine/palladium-catalyzed one-pot synthesis of functionalized 6H-benzo[c]chromenes." RSC Advances 5, no. 71 (2015): 57462–68. http://dx.doi.org/10.1039/c5ra10550a.

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43

Aneeja, Thaipparambil, Sankaran Radhika, Mohan Neetha, and Gopinathan Anilkumar. "An Overview of the One-pot Synthesis of Imidazolines." Current Organic Chemistry 24, no. 20 (December 2, 2020): 2341–55. http://dx.doi.org/10.2174/1385272824999201001153735.

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One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.
44

Aneeja, Thaipparambil, Sankaran Radhika, Mohan Neetha, and Gopinathan Anilkumar. "An Overview of the One-pot Synthesis of Imidazolines." Current Organic Chemistry 24, no. 20 (October 2020): 2341–55. http://dx.doi.org/10.2174/138527282499920100115373.

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One-pot syntheses are a simple, efficient and easy methodology, which are widely used for the synthesis of organic compounds. Imidazoline is a valuable heterocyclic moiety used as a synthetic intermediate, chiral auxiliary, chiral catalyst and a ligand for asymmetric catalysis. Imidazole is a fundamental unit of biomolecules that can be easily prepared from imidazolines. The one-pot method is an impressive approach to synthesize organic compounds as it minimizes the reaction time, separation procedures, and ecological impact. Many significant one-pot methods such as N-bromosuccinimide mediated reaction, ring-opening of tetrahydrofuran, triflic anhydrate mediated reaction, etc. were reported for imidazoline synthesis. This review describes an overview of the one-pot synthesis of imidazolines and covers literature up to 2020.
45

Kwon, Yearang, Mina Jeon, Jin Yong Park, Young Ho Rhee, and Jaiwook Park. "Synthesis of 1H-azadienes and application to one-pot organic transformations." RSC Advances 6, no. 1 (2016): 661–68. http://dx.doi.org/10.1039/c5ra26230e.

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1H-Azadienes were synthesized from allyl azides by ruthenium catalysis under mild and neutral conditions. Applications of the 1H-azadienes were demonstrated for the one-pot synthesis of nitrogen containing organic compounds.
46

Harmata, Michael, and Neville Pavri. "A One-Pot, One-Operation [3+3] Annulation Approach to Benzothiazines." Angewandte Chemie International Edition 38, no. 16 (August 16, 1999): 2419–21. http://dx.doi.org/10.1002/(sici)1521-3773(19990816)38:16<2419::aid-anie2419>3.0.co;2-i.

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47

Fathi Vavsari, Vaezeh, Mehri Seyed Hashtroudi, and Saeed Balalaie. "Ru-Catalyzed One-Pot Synthesis of Heterocyclic Backbones." Catalysts 13, no. 1 (January 1, 2023): 87. http://dx.doi.org/10.3390/catal13010087.

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Ruthenium complexes are remarkable catalysts for the C–H activation approaches and organic transformations. Combining a Ru-catalyst with oxidants and other additives in a one-pot process is considered a sustainable approach due to the reduction in reaction steps and the minimal usage of solvents during synthesis, work-up, isolation of chemicals, and purification of the products. This review highlights the ruthenium-catalyzed organic transformations in a one-pot manner to achieve heterocyclic backbones, including indoles, benzofurans, indazoles, pyrans, pyrimidines, quinolines, and isoquinolines.
48

Akkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith, and Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols." Synthesis 52, no. 05 (January 7, 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.

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The Suzuki–Miyaura reaction is one of the most powerful tools for the formation of carbon–carbon bonds in organic synthesis. The utilization of alcohols in this powerful reaction is a challenging task. This short review covers progress in the transition-metal-catalyzed Suzuki­–Miyaura-type cross-coupling reaction of π-activated alcohol, such as aryl, benzylic, allylic, propargylic and allenic alcohols, between 2000 and June 2019.1 Introduction2 Suzuki–Miyaura Cross-Coupling Reactions of Aryl Alcohols2.1 One-Pot Reactions with Pre-activation of the C–O Bond2.1.1 Palladium Catalysis2.1.2 Nickel Catalysis2.2 Direct Activation of the C–O Bond2.2.1 Nickel Catalysis3 Suzuki–Miyaura-Type Cross-Coupling Reactions of Benzylic Alcohols4 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allylic Alcohols4.1 Rhodium Catalysis4.2 Palladium Catalysis4.3 Nickel Catalysis4.4 Stereospecific Reactions4.5 Stereoselective Reactions4.6 Domino Reactions5 Suzuki–Miyaura-Type Cross-Coupling Reactions of Propargylic Alcohols5.1 Palladium Catalysis5.2 Rhodium Catalysis6 Suzuki–Miyaura-Type Cross-Coupling Reactions of Allenic Alcohols6.1 Palladium Catalysis6.2 Rhodium Catalysis7 Conclusions
49

Suresh, Pavithira, and Subramaniapillai Selva Ganesan. "Lipophilic NHC assisted one-pot synthesis of syncarpamide analogues in aqueous medium." New Journal of Chemistry 43, no. 16 (2019): 6257–61. http://dx.doi.org/10.1039/c9nj00134d.

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50

Li, An-Hu, David Beard, Heather Coate, Ayako Honda, Mridula Kadalbajoo, Andrew Kleinberg, Radoslaw Laufer, et al. "One-Pot Friedländer Quinoline Synthesis: Scope and Limitations." Synthesis 2010, no. 10 (March 12, 2010): 1678–86. http://dx.doi.org/10.1055/s-0029-1218701.

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