Artigos de revistas sobre o tema "One-pot catalysis"
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Choi, Youngbo, Yang Sik Yun, Hongseok Park, Dae Sung Park, Danim Yun e Jongheop Yi. "A facile approach for the preparation of tunable acid nano-catalysts with a hierarchically mesoporous structure". Chem. Commun. 50, n.º 57 (2014): 7652–55. http://dx.doi.org/10.1039/c4cc01881h.
Texto completo da fonteKumar, Devarapalli Ravi, e Gedu Satyanarayana. "Palladium Catalysis: One‐Pot Synthesis of Fluorenones". ChemistrySelect 3, n.º 27 (18 de julho de 2018): 7867–70. http://dx.doi.org/10.1002/slct.201801787.
Texto completo da fonteZhang, Luxin, Xu Xing, Ruijun Sun e Meng Hu. "Catalytic conversion of carbohydrates into 5-ethoxymethylfurfural using γ-AlOOH and CeO2@B2O3 catalyst synergistic effect". RSC Advances 12, n.º 36 (2022): 23118–28. http://dx.doi.org/10.1039/d2ra01866g.
Texto completo da fonteSau, Samaresh Chandra, Sudipta Raha Roy e Swadhin K. Mandal. "One-Pot Consecutive Catalysis by Integrating Organometallic Catalysis with Organocatalysis". Chemistry - An Asian Journal 9, n.º 10 (14 de agosto de 2014): 2806–13. http://dx.doi.org/10.1002/asia.201402363.
Texto completo da fontePellissier, Hélène. "Asymmetric Zinc Catalysis in Green One-pot Processes". Current Organic Chemistry 25, n.º 8 (28 de abril de 2021): 857–75. http://dx.doi.org/10.2174/1385272825666210216123607.
Texto completo da fonteDe Nisi, A., S. Sierra, M. Ferrara, M. Monari e M. Bandini. "TBAF catalyzed one-pot synthesis of allenyl-indoles". Organic Chemistry Frontiers 4, n.º 9 (2017): 1849–53. http://dx.doi.org/10.1039/c7qo00414a.
Texto completo da fonteProchazka, Michal P., Rolf Carlson, Pentti Mälkönen, Heikki Hukkanen, M. Nielsen, M. S. Lehmann e 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.
Texto completo da fonteGao, Xiang, e Henri B. Kagan. "One-pot multi-substrate screening in asymmetric catalysis". Chirality 10, n.º 1-2 (1998): 120–24. http://dx.doi.org/10.1002/chir.19.
Texto completo da fonteGao, Xiang, e Henri B. Kagan. "One‐pot multi‐substrate screening in asymmetric catalysis". Chirality 10, n.º 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.
Texto completo da fonteHou, Fang, Wei Zheng e 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, n.º 1 (3 de janeiro de 2020): 199–212. http://dx.doi.org/10.9767/bcrec.15.1.6179.199-212.
Texto completo da fonteFaul, Dieter, Edith Leber e Gerhard Himbert. "One-Pot Synthesis of Hexatriynediamines". Synthesis 1987, n.º 01 (1987): 73–74. http://dx.doi.org/10.1055/s-1987-27853.
Texto completo da fonteNiu, Chengrong, Jie Hu, Yinfeng Li, Jinghang Leng e Songjun Li. "A thermoresponsive nanorattle containing two different catalysts for controllable one-pot tandem catalysis". Nanotechnology 29, n.º 10 (30 de janeiro de 2018): 105501. http://dx.doi.org/10.1088/1361-6528/aaa3d2.
Texto completo da fonteTang, Xinxin, Lan Gan, Xin Zhang e Zheng Huang. "n-Alkanes to n-alcohols: Formal primary C─H bond hydroxymethylation via quadruple relay catalysis". Science Advances 6, n.º 47 (novembro de 2020): eabc6688. http://dx.doi.org/10.1126/sciadv.abc6688.
Texto completo da fonteCorma, Avelino, Javier Navas e Maria J. Sabater. "Advances in One-Pot Synthesis through Borrowing Hydrogen Catalysis". Chemical Reviews 118, n.º 4 (10 de janeiro de 2018): 1410–59. http://dx.doi.org/10.1021/acs.chemrev.7b00340.
Texto completo da fonteBallini, Roberto, Giovanna Bosica, Dennis Fiorini e Alessandro Palmieri. "One-Pot Synthesis of 1,3-Dinitroalkanes under Heterogeneous Catalysis". Synthesis 2004, n.º 12 (21 de julho de 2004): 1938–40. http://dx.doi.org/10.1055/s-2004-829160.
Texto completo da fonteHashmi, A. Stephen K., e Anna Littmann. "Gold Catalysis: One-Pot Alkylideneoxazoline Synthesis/Alder-Ene Reaction". Chemistry - An Asian Journal 7, n.º 6 (20 de março de 2012): 1435–42. http://dx.doi.org/10.1002/asia.201200046.
Texto completo da fonteXiao, Xiong, Jing Zeng, Jing Fang, Jiuchang Sun, Ting Li, Zejin Song, Lei Cai e Qian Wan. "One-Pot Relay Glycosylation". Journal of the American Chemical Society 142, n.º 12 (9 de março de 2020): 5498–503. http://dx.doi.org/10.1021/jacs.0c00447.
Texto completo da fonteParenty, Alexis, e Leroy Cronin. "One-Pot Synthesis of Imidazopyridine Derivatives". Synthesis 2008, n.º 9 (maio de 2008): 1479–85. http://dx.doi.org/10.1055/s-2007-1000936.
Texto completo da fonteBayarmagnai, Bilguun, Christian Matheis, Eugen Risto e Lukas J. Goossen. "One-Pot Sandmeyer Trifluoromethylation and Trifluoromethylthiolation". Advanced Synthesis & Catalysis 356, n.º 10 (20 de junho de 2014): 2343–48. http://dx.doi.org/10.1002/adsc.201400340.
Texto completo da fonteShu, Fan, Qingjuan Zheng, Wanrong Dong, Zhihong Peng e Delie An. "One-pot synthesis of propynoates and propynenitriles". Canadian Journal of Chemistry 95, n.º 2 (fevereiro de 2017): 144–48. http://dx.doi.org/10.1139/cjc-2016-0181.
Texto completo da fontePirouz, Maryam, M. Saeed Abaee, Pernille Harris e Mohammad M. Mojtahedi. "One-pot synthesis of benzofurans via heteroannulation of benzoquinones". Heterocyclic Communications 27, n.º 1 (1 de janeiro de 2021): 24–31. http://dx.doi.org/10.1515/hc-2020-0120.
Texto completo da fonteLuan, Huimin, Chi Lei, Qinming Wu, Na Sheng, Yeqing Wang, Xiangju Meng e Feng-Shou Xiao. "Sustainable one-pot preparation of fully crystalline shaped zeolite catalysts". Catalysis Science & Technology 11, n.º 16 (2021): 5650–55. http://dx.doi.org/10.1039/d1cy00948f.
Texto completo da fonteSzőllősi, György. "Asymmetric one-pot reactions using heterogeneous chemical catalysis: recent steps towards sustainable processes". Catalysis Science & Technology 8, n.º 2 (2018): 389–422. http://dx.doi.org/10.1039/c7cy01671a.
Texto completo da fonteCao, Yueling, Hepeng Zhang, Kangkai Liu e Kai-Jie Chen. "Water-assisted one-pot synthesis of N-doped carbon supported Ru catalysts for heterogeneous catalysis". Chemical Communications 56, n.º 76 (2020): 11311–14. http://dx.doi.org/10.1039/d0cc04743k.
Texto completo da fonteChatterjee, Basujit, Deepti Kalsi, Akash Kaithal, Alexis Bordet, Walter Leitner e Chidambaram Gunanathan. "One-pot dual catalysis for the hydrogenation of heteroarenes and arenes". Catalysis Science & Technology 10, n.º 15 (2020): 5163–70. http://dx.doi.org/10.1039/d0cy00928h.
Texto completo da fonteZhao, Xinpeng, Wang Liu, Lijun Zhu, Yanfei Zhang, Mengya Sun, Gai Miao, Hu Luo, Shenggang Li e Lingzhao Kong. "Efficient one-pot tandem catalysis of glucose into 1,1,2-trimethoxyethane over W-Beta catalysts". Sustainable Energy & Fuels 6, n.º 4 (2022): 1051–57. http://dx.doi.org/10.1039/d1se02048j.
Texto completo da fonteMotokura, Ken. "Development of Multiactive Site Catalysts for Surface Concerted Catalysis Aimed at One-Pot Synthesis". Bulletin of the Chemical Society of Japan 90, n.º 2 (15 de fevereiro de 2017): 137–47. http://dx.doi.org/10.1246/bcsj.20160291.
Texto completo da fonteRen, Yufeng, Wei Zhang, Jun Lu, Kai Gao, Xiali Liao e Xiaozhen Chen. "One-pot synthesis of tetrahydro-4H-chromenes by supramolecular catalysis in water". RSC Advances 5, n.º 97 (2015): 79405–12. http://dx.doi.org/10.1039/c5ra14385c.
Texto completo da fonteDavies, Alyn T., John M. Curto, Scott W. Bagley e Michael C. Willis. "One-pot palladium-catalyzed synthesis of sulfonyl fluorides from aryl bromides". Chemical Science 8, n.º 2 (2017): 1233–37. http://dx.doi.org/10.1039/c6sc03924c.
Texto completo da fonteCui, Hai-Lei, e Fujie Tanaka. "One-pot synthesis of polysubstituted 3-acylpyrroles by cooperative catalysis". Org. Biomol. Chem. 12, n.º 31 (2014): 5822–26. http://dx.doi.org/10.1039/c4ob01019a.
Texto completo da fonteLi, Yong-Qi, Peng Wang, Huan Liu, Yong Lu, Xiao-Li Zhao e Ye Liu. "Co-catalysis of a bi-functional ligand containing phosphine and Lewis acidic phosphonium for hydroformylation–acetalization of olefins". Green Chemistry 18, n.º 6 (2016): 1798–806. http://dx.doi.org/10.1039/c5gc02127h.
Texto completo da fonteRene, Loic, Joël Poncet e Gilles Auzou. "A One Pot Synthesis of β-Cyanoenamines". Synthesis 1986, n.º 05 (1986): 419–20. http://dx.doi.org/10.1055/s-1986-31661.
Texto completo da fonteEl Cherif, Souheir, e Loïc René. "A One-Pot Synthesis of β-Acylenamines". Synthesis 1988, n.º 02 (1988): 138–40. http://dx.doi.org/10.1055/s-1988-27492.
Texto completo da fonteDehmlow, E. V., U. Fastabend e M. Keßler. "A One-Pot Synthesis of Trimethylsilyl Fluoride". Synthesis 1988, n.º 12 (1988): 996–97. http://dx.doi.org/10.1055/s-1988-27783.
Texto completo da fonteHudson, Richard, David Fouchard e L. Tillekeratne. "An Efficient One-Pot Synthesis of Aminobenzimidazoles". Synthesis 2005, n.º 01 (17 de novembro de 2004): 17–18. http://dx.doi.org/10.1055/s-2004-834925.
Texto completo da fonteHandy, Scott, e Samantha Anderson. "One-Pot Double Suzuki Couplings of Dichloropyrimidines". Synthesis 2010, n.º 16 (7 de julho de 2010): 2721–24. http://dx.doi.org/10.1055/s-0030-1258150.
Texto completo da fonteSchmalz, Hans-Günther, e Peter Huy. "Practical One-Pot Double Functionalizations of Proline". Synthesis 2011, n.º 06 (10 de fevereiro de 2011): 954–60. http://dx.doi.org/10.1055/s-0030-1258428.
Texto completo da fonteKorpak, Margarete, e Jörg Pietruszka. "Chemoenzymatic One-Pot Synthesis of γ-Butyrolactones". Advanced Synthesis & Catalysis 353, n.º 9 (junho de 2011): 1420–24. http://dx.doi.org/10.1002/adsc.201100110.
Texto completo da fontePeterson, Geneva R, e Nick Bampos. "One-Pot Synthesis of Indene-Expanded Porphyrins". Angewandte Chemie International Edition 49, n.º 23 (10 de maio de 2010): 3930–33. http://dx.doi.org/10.1002/anie.200906580.
Texto completo da fonteMatsumoto, Kazuhiro, Yuki Oba, Yumiko Nakajima, Shigeru Shimada e Kazuhiko Sato. "One-Pot Sequence-Controlled Synthesis of Oligosiloxanes". Angewandte Chemie International Edition 57, n.º 17 (15 de março de 2018): 4637–41. http://dx.doi.org/10.1002/anie.201801031.
Texto completo da fonteInamdar, Suleman M., Ashok Konala e Nitin T. Patil. "When gold meets chiral Brønsted acid catalysts: extending the boundaries of enantioselective gold catalysis". Chem. Commun. 50, n.º 96 (2014): 15124–35. http://dx.doi.org/10.1039/c4cc04633a.
Texto completo da fonteMo, Hanjie, Chengmin Pan, Dingben Chen, Di Chen, Jianrong Gao e Jianguo Yang. "Phosphine/palladium-catalyzed one-pot synthesis of functionalized 6H-benzo[c]chromenes". RSC Advances 5, n.º 71 (2015): 57462–68. http://dx.doi.org/10.1039/c5ra10550a.
Texto completo da fonteAneeja, Thaipparambil, Sankaran Radhika, Mohan Neetha e Gopinathan Anilkumar. "An Overview of the One-pot Synthesis of Imidazolines". Current Organic Chemistry 24, n.º 20 (2 de dezembro de 2020): 2341–55. http://dx.doi.org/10.2174/1385272824999201001153735.
Texto completo da fonteAneeja, Thaipparambil, Sankaran Radhika, Mohan Neetha e Gopinathan Anilkumar. "An Overview of the One-pot Synthesis of Imidazolines". Current Organic Chemistry 24, n.º 20 (outubro de 2020): 2341–55. http://dx.doi.org/10.2174/138527282499920100115373.
Texto completo da fonteKwon, Yearang, Mina Jeon, Jin Yong Park, Young Ho Rhee e Jaiwook Park. "Synthesis of 1H-azadienes and application to one-pot organic transformations". RSC Advances 6, n.º 1 (2016): 661–68. http://dx.doi.org/10.1039/c5ra26230e.
Texto completo da fonteHarmata, Michael, e Neville Pavri. "A One-Pot, One-Operation [3+3] Annulation Approach to Benzothiazines". Angewandte Chemie International Edition 38, n.º 16 (16 de agosto de 1999): 2419–21. http://dx.doi.org/10.1002/(sici)1521-3773(19990816)38:16<2419::aid-anie2419>3.0.co;2-i.
Texto completo da fonteFathi Vavsari, Vaezeh, Mehri Seyed Hashtroudi e Saeed Balalaie. "Ru-Catalyzed One-Pot Synthesis of Heterocyclic Backbones". Catalysts 13, n.º 1 (1 de janeiro de 2023): 87. http://dx.doi.org/10.3390/catal13010087.
Texto completo da fonteAkkarasamiyo, Sunisa, Somsak Ruchirawat, Poonsaksi Ploypradith e Joseph S. M. Samec. "Transition-Metal-Catalyzed Suzuki–Miyaura-Type Cross-Coupling Reactions of π-Activated Alcohols". Synthesis 52, n.º 05 (7 de janeiro de 2020): 645–59. http://dx.doi.org/10.1055/s-0039-1690740.
Texto completo da fonteSuresh, Pavithira, e Subramaniapillai Selva Ganesan. "Lipophilic NHC assisted one-pot synthesis of syncarpamide analogues in aqueous medium". New Journal of Chemistry 43, n.º 16 (2019): 6257–61. http://dx.doi.org/10.1039/c9nj00134d.
Texto completo da fonteLi, 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, n.º 10 (12 de março de 2010): 1678–86. http://dx.doi.org/10.1055/s-0029-1218701.
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