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Artigos de revistas sobre o tema "Dioxazolone"

Autor: Grafiati

Publicado: 19 de outubro de 2024

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1

Borah, Gongutri, Preetismita Borah e Pitambar Patel. "Cp*Co(iii)-catalyzed ortho-amidation of azobenzenes with dioxazolones". Organic & Biomolecular Chemistry 15, n.º 18 (2017): 3854–59. http://dx.doi.org/10.1039/c7ob00540g.

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2

Zhang, Lei, Xiangyun Zheng, Jinkang Chen, Kang Cheng, Licheng Jin, Xinpeng Jiang e Chuanming Yu. "Ru(ii)-Catalyzed C6-selective C–H amidation of 2-pyridones". Organic Chemistry Frontiers 5, n.º 20 (2018): 2969–73. http://dx.doi.org/10.1039/c8qo00795k.

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3

Pan, Deng, Gen Luo, Yang Yu, Jimin Yang e Yi Luo. "Computational insights into Ir(iii)-catalyzed allylic C–H amination of terminal alkenes: mechanism, regioselectivity, and catalytic activity". RSC Advances 11, n.º 31 (2021): 19113–20. http://dx.doi.org/10.1039/d1ra03842g.

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DFT studies on Ir(iii)-catalyzed branch-selective allylic C–H amination of terminal olefins with methyl dioxazolone have been carried out to investigate the mechanism, including the origins of regioselectivity and catalytic activity difference.

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4

Hall, David S., Toren Hynes e J. R. Dahn. "Dioxazolone and Nitrile Sulfite Electrolyte Additives for Lithium-Ion Cells". Journal of The Electrochemical Society 165, n.º 13 (2018): A2961—A2967. http://dx.doi.org/10.1149/2.0341813jes.

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5

Gauthier, Roby, David S. Hall, Katherine Lin, Jazmin Baltazar, Toren Hynes e J. R. Dahn. "Impact of Functionalization and Co-Additives on Dioxazolone Electrolyte Additives". Journal of The Electrochemical Society 167, n.º 8 (26 de maio de 2020): 080540. http://dx.doi.org/10.1149/1945-7111/ab8ed6.

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6

Ghosh, Payel, Sadhanendu Samanta e Alakananda Hajra. "Rhodium(iii)-catalyzed ortho-C–H amidation of 2-arylindazoles with a dioxazolone as an amidating reagent". Organic & Biomolecular Chemistry 18, n.º 9 (2020): 1728–32. http://dx.doi.org/10.1039/c9ob02756d.

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A simple and efficient method for directed amidation of a wide range of 2-arylindazoles has been established for the first time through a rhodium-catalyzed C–H activation reaction with alkyl, aryl and heteroaryl dioxazolones.

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7

Hande, Akshay Ekanath, Nachimuthu Muniraj e Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C-H Amidation of Azobenzene Derivatives Using Dioxazolone as an Amidating Reagent". ChemistrySelect 2, n.º 21 (21 de julho de 2017): 5965–69. http://dx.doi.org/10.1002/slct.201701277.

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8

Hande, Akshay Ekanath, e Kandikere Ramaiah Prabhu. "Ru(II)-Catalyzed C–H Amidation of Indoline at the C7-Position Using Dioxazolone as an Amidating Agent: Synthesis of 7-Amino Indoline Scaffold". Journal of Organic Chemistry 82, n.º 24 (28 de novembro de 2017): 13405–13. http://dx.doi.org/10.1021/acs.joc.7b02500.

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9

Liu, Chen-Fei, Man Liu, Jun-Shu Sun, Chao Li e Lin Dong. "Synthesis of 2-aminobenzaldehydes by rhodium(iii)-catalyzed C–H amidation of aldehydes with dioxazolones". Organic Chemistry Frontiers 5, n.º 13 (2018): 2115–19. http://dx.doi.org/10.1039/c8qo00413g.

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10

Tang, Shi-Biao, Xiao-Pan Fu, Gao-Rong Wu, Li-Li Zhang, Ke-Zuan Deng, Jin-Yue Yang, Cheng-Cai Xia e Ya-Fei Ji. "Rhodium(iii)-catalyzed C4-amidation of indole-oximes with dioxazolones via C–H activation". Organic & Biomolecular Chemistry 18, n.º 39 (2020): 7922–31. http://dx.doi.org/10.1039/d0ob01655a.

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11

Saxena, Paridhi, Neha Maida e Manmohan Kapur. "Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C–H arylation of 6,5-fused heterocycles". Chemical Communications 55, n.º 75 (2019): 11187–90. http://dx.doi.org/10.1039/c9cc05563k.

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12

Wang, Jinlei, Guangfan Zheng e Xingwei Li. "Rhodium(iii)-catalyzed diamidation of olefins via amidorhodation and further amidation". Chemical Communications 56, n.º 56 (2020): 7809–12. http://dx.doi.org/10.1039/d0cc00952k.

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13

Liu, Yuan, Fang Xie, Ai-Qun Jia e Xingwei Li. "Cp*Co(iii)-catalyzed amidation of olefinic and aryl C–H bonds: highly selective synthesis of enamides and pyrimidones". Chemical Communications 54, n.º 34 (2018): 4345–48. http://dx.doi.org/10.1039/c8cc01447g.

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14

Song, Dan, Changfeng Huang, Peishi Liang, Baofu Zhu, Xiang Liu e Hua Cao. "Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement". Organic Chemistry Frontiers 8, n.º 11 (2021): 2583–88. http://dx.doi.org/10.1039/d1qo00224d.

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An efficient, direct, and novel Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement under metal-free conditions has been documented.

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15

Tobisch, Sven. "Copper hydride-mediated electrophilic amidation of vinylarenes with dioxazolones – a computational mechanistic study". Dalton Transactions 48, n.º 38 (2019): 14337–46. http://dx.doi.org/10.1039/c9dt02540e.

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An in-depth computational mechanistic probe of the CuH-mediated formal hydroamidation of vinylarenes with dioxazolones allowed the substitution of mechanistic hypothesis advanced previously by a computationally verified mechanistic view.

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16

Ding, Jun, Wei Jiang, He-Yuan Bai, Tong-Mei Ding, Dafang Gao, Xiaoguang Bao e Shu-Yu Zhang. "Experimental and computational studies on H2O-promoted, Rh-catalyzed transient-ligand-free ortho-C(sp2)–H amidation of benzaldehydes with dioxazolones". Chemical Communications 54, n.º 64 (2018): 8889–92. http://dx.doi.org/10.1039/c8cc04904a.

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17

Bae, Hyeonwoong, Jinhwan Park, Rahyun Yoon, Seunghoon Lee e Jongwoo Son. "Copper-catalyzed synthesis of primary amides through reductive N–O cleavage of dioxazolones". RSC Advances 14, n.º 14 (2024): 9440–44. http://dx.doi.org/10.1039/d4ra00320a.

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Reaction of dioxazolones in the presence of a copper catalyst and a silane is represented. Mild reductive reaction conditions for the N–O bond cleavage and large-scale protocols are also highlighted with excellent tolerance in the presence of water.

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18

Yetra, Santhivardhana Reddy, Zhigao Shen, Hui Wang e Lutz Ackermann. "Thiocarbonyl-enabled ferrocene C–H nitrogenation by cobalt(III) catalysis: thermal and mechanochemical". Beilstein Journal of Organic Chemistry 14 (25 de junho de 2018): 1546–53. http://dx.doi.org/10.3762/bjoc.14.131.

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Versatile C–H amidations of synthetically useful ferrocenes were accomplished by weakly-coordinating thiocarbonyl-assisted cobalt catalysis. Thus, carboxylates enabled ferrocene C–H nitrogenations with dioxazolones, featuring ample substrate scope and robust functional group tolerance. Mechanistic studies provided strong support for a facile organometallic C–H activation manifold.

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19

Bondock, Samir, Ehab Abdel Latif e Johann Lex. "Solvent-free Photooxygenation of 5-methoxyoxazoles: Stereoselective Synthesis of α-amino-α-hydroxy Carboxylic Acid Derivatives". Journal of Chemical Research 2005, n.º 7 (julho de 2005): 422–26. http://dx.doi.org/10.3184/030823405774309168.

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A solvent-free photooxygenation of 5-methoxyoxazoles 1a–j embedded in porphrin-loaded polystyrene beads as solid support is described and applied for the synthesis of 3H-1,2,4-dioxazole derivatives 2a–j. Acid catalysed hydrolysis of 3H-1,2,4-dioxazole derivatives gave α-amino-α-hydroxy carboxylic acid derivatives 3a–j. The structural elucidation of the new compounds were carried on the basis of spectral and X-ray analyses.

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20

Pan, Jie, Haocong Li, Kai Sun, Shi Tang e Bing Yu. "Visible-Light-Induced Decarboxylation of Dioxazolones to Phosphinimidic Amides and Ureas". Molecules 27, n.º 12 (7 de junho de 2022): 3648. http://dx.doi.org/10.3390/molecules27123648.

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A visible-light-induced external catalyst-free decarboxylation of dioxazolones was realized for the bond formation of N=P and N–C bonds to access phosphinimidic amides and ureas. Various phosphinimidic amides and ureas (47 examples) were synthesized with high yields (up to 98%) by this practical strategy in the presence of the system’s ppm Fe.

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21

Colbeaux, Aimeline, Françoise Fenouillot, Jean-François Gerard, Mohamed Taha e Henri Wautier. "Dioxazoline coupling of maleic anhydride modified polyethylene". Journal of Applied Polymer Science 97, n.º 3 (2005): 837–43. http://dx.doi.org/10.1002/app.21793.

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22

Nishii, Yuji, Masahiro Miura, Chandrababu Naidu Kona e Rikuto Oku. "Peri-Selective Direct Acylmethylation and Amidation of Naphthalene Derivatives Using Iridium and Rhodium Catalysts". Synthesis 53, n.º 17 (31 de março de 2021): 3126–36. http://dx.doi.org/10.1055/a-1472-1059.

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AbstractAn iridium-catalyzed acylmethylation and a rhodium-catalyzed amidation of naphthalene derivatives are reported, adopting sulfoxonium ylides and dioxazolones as carbene and nitrene transfer agents, respectively. The use of SMe group as a directing group was key to ensure the peri-selective functionalization, and it can be easily removed or diversely transformed to other synthetically useful functionalities after the catalysis.

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23

Liao, Xian-Zhang, Man Liu e Lin Dong. "An Approach to Vinylidenequinazolines from Isoxazoles and Dioxazolones". Journal of Organic Chemistry 87, n.º 5 (28 de janeiro de 2022): 3741–50. http://dx.doi.org/10.1021/acs.joc.1c02746.

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24

van Vliet, Kaj M., e Bas de Bruin. "Dioxazolones: Stable Substrates for the Catalytic Transfer of Acyl Nitrenes". ACS Catalysis 10, n.º 8 (30 de março de 2020): 4751–69. http://dx.doi.org/10.1021/acscatal.0c00961.

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25

Samanta, Sadhanendu, Susmita Mondal, Debashis Ghosh e Alakananda Hajra. "Rhodium-Catalyzed Directed C–H Amidation of Imidazoheterocycles with Dioxazolones". Organic Letters 21, n.º 12 (12 de junho de 2019): 4905–9. http://dx.doi.org/10.1021/acs.orglett.9b01832.

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26

Mi, Xia, Weisheng Feng, Chao Pi e Xiuling Cui. "Iridium(III)-Catalyzed C–H Amidation of Nitrones with Dioxazolones". Journal of Organic Chemistry 84, n.º 9 (4 de abril de 2019): 5305–12. http://dx.doi.org/10.1021/acs.joc.9b00300.

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27

Chen, Jiajia, e Yuanzhi Xia. "Visible-Light-Induced Iron Catalysis for Nitrene Transfer Reactions with Dioxazolones". Chinese Journal of Organic Chemistry 41, n.º 9 (2021): 3748. http://dx.doi.org/10.6023/cjoc202100069.

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28

Jeoung, Daeun, Kunyoung Kim, Sang Hoon Han, Prithwish Ghosh, Suk Hun Lee, Saegun Kim, Won An, Hyung Sik Kim, Neeraj Kumar Mishra e In Su Kim. "Phthalazinone-Assisted C–H Amidation Using Dioxazolones Under Rh(III) Catalysis". Journal of Organic Chemistry 85, n.º 11 (10 de abril de 2020): 7014–23. http://dx.doi.org/10.1021/acs.joc.0c00352.

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29

Huang, Yanzhen, Chao Pi, Zhen Tang, Yangjie Wu e Xiuling Cui. "Cp*Co(III)-catalyzed C H amidation of azines with dioxazolones". Chinese Chemical Letters 31, n.º 12 (dezembro de 2020): 3237–40. http://dx.doi.org/10.1016/j.cclet.2020.08.046.

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30

Chalamet, Yvan, e Mohamed Taha. "Carboxyl terminated polyamide 12 chain extension using a dioxazoline coupling agent". Journal of Polymer Science Part A: Polymer Chemistry 35, n.º 17 (dezembro de 1997): 3697–705. http://dx.doi.org/10.1002/(sici)1099-0518(199712)35:17<3697::aid-pola9>3.0.co;2-p.

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31

Mishra, Neeraj Kumar, Yongguk Oh, Mijin Jeon, Sangil Han, Satyasheel Sharma, Sang Hoon Han, Sung Hee Um e In Su Kim. "Site-Selective C-H Amidation of Azobenzenes with Dioxazolones under Rhodium Catalysis". European Journal of Organic Chemistry 2016, n.º 29 (27 de setembro de 2016): 4976–80. http://dx.doi.org/10.1002/ejoc.201601096.

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32

Tang, Jing‐Jing, Xiaoqiang Yu, Yi Wang, Yoshinori Yamamoto e Ming Bao. "Interweaving Visible‐Light and Iron Catalysis for Nitrene Formation and Transformation with Dioxazolones". Angewandte Chemie 133, n.º 30 (10 de maio de 2021): 16562–71. http://dx.doi.org/10.1002/ange.202016234.

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33

Tang, Jing‐Jing, Xiaoqiang Yu, Yi Wang, Yoshinori Yamamoto e Ming Bao. "Interweaving Visible‐Light and Iron Catalysis for Nitrene Formation and Transformation with Dioxazolones". Angewandte Chemie International Edition 60, n.º 30 (10 de maio de 2021): 16426–35. http://dx.doi.org/10.1002/anie.202016234.

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34

Han, Gi Uk, Seohyun Shin, Yonghyeon Baek, Dongwook Kim, Kooyeon Lee, Jeung Gon Kim e Phil Ho Lee. "Mechanochemical Iridium(III)-Catalyzed B-Amidation of o-Carboranes with Dioxazolones". Organic Letters 23, n.º 21 (18 de outubro de 2021): 8622–27. http://dx.doi.org/10.1021/acs.orglett.1c03336.

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35

Jeon, Bomi, Uiseong Yeon, Jeong-Yu Son e Phil Ho Lee. "Selective Rhodium-Catalyzed C–H Amidation of Azobenzenes with Dioxazolones under Mild Conditions". Organic Letters 18, n.º 18 (26 de agosto de 2016): 4610–13. http://dx.doi.org/10.1021/acs.orglett.6b02250.

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36

Chamni, Supakarn, Jinquan Zhang e Hongbin Zou. "Benign synthesis of unsymmetrical arylurea derivatives using 3-substituted dioxazolones as isocyanate surrogates". Green Chemistry Letters and Reviews 13, n.º 3 (2 de julho de 2020): 246–57. http://dx.doi.org/10.1080/17518253.2020.1807616.

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37

Wang, Xiaoyang, Song Song e Ning Jiao. "Rh-catalyzed Transient Directing Group Promoted C-H Amidation of Benzaldehydes Utilizing Dioxazolones". Chinese Journal of Chemistry 36, n.º 3 (11 de janeiro de 2018): 213–16. http://dx.doi.org/10.1002/cjoc.201700726.

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38

Guo, Wusheng, e Biwei Yan. "Recent Advances in Decarboxylative Conversions of Cyclic Carbonates and Beyond". Synthesis 54, n.º 08 (7 de dezembro de 2021): 1964–76. http://dx.doi.org/10.1055/a-1715-7413.

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AbstractIn recent years, functionalized cyclic organic carbonates have emerged as valuable building blocks for the construction of interesting and useful molecules upon decarboxylation under transition-metal catalysis. By employing suitable catalytic systems, the development of chemo-, regio-, stereo- and enantioselective methods for the synthesis of useful and interesting compounds has advanced greatly. On the basis of previous research on this topic, this short review highlights the synthetic potential of cyclic carbonates under transition-metal catalysis over the last two years.1 Introduction2 Transition-Metal-Catalyzed Decarboxylation of Vinyl Cyclic Carbonates3 Zwitterionic Enolate Chemistry Based On Transition-Metal Catalysis4 Decarboxylation of Alkynyl Cyclic Carbonates and Dioxazolones5 Conclusions and Perspectives

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39

Sheng, Yaoguang, Jianmin Zhou, Yi Gao, Bingbing Duan, Yi Wang, Aleksandr Samorodov, Guang Liang, Qiuhua Zhao e Zengqiang Song. "Ruthenium(II)-Catalyzed Direct C7-Selective Amidation of Indoles with Dioxazolones at Room Temperature". Journal of Organic Chemistry 86, n.º 3 (20 de janeiro de 2021): 2827–39. http://dx.doi.org/10.1021/acs.joc.0c02779.

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40

Tang, Jing-Jing, Xiaoqiang Yu, Yoshinori Yamamoto e Ming Bao. "Visible-Light-Promoted Iron-Catalyzed N-Arylation of Dioxazolones with Arylboronic Acids". ACS Catalysis 11, n.º 22 (3 de novembro de 2021): 13955–61. http://dx.doi.org/10.1021/acscatal.1c04538.

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41

Lee, Sumin, e Tomislav Rovis. "Rh(III)-Catalyzed Three-Component Syn-Carboamination of Alkenes Using Arylboronic Acids and Dioxazolones". ACS Catalysis 11, n.º 14 (30 de junho de 2021): 8585–90. http://dx.doi.org/10.1021/acscatal.1c02406.

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42

Wang, Jie, Shanke Zha, Kehao Chen, Feifei Zhang, Chao Song e Jin Zhu. "Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C–H Functionalization of Benzimidates with Dioxazolones". Organic Letters 18, n.º 9 (8 de abril de 2016): 2062–65. http://dx.doi.org/10.1021/acs.orglett.6b00691.

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43

Schroth, Werner, e Olaf Peters. "2-Acylmethyl-1, 3, 4-dioxazole durch Ketovinylierung von Hydroxamsäuren". Zeitschrift für Chemie 18, n.º 2 (1 de setembro de 2010): 57–58. http://dx.doi.org/10.1002/zfch.19780180204.

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44

Huang, Jie, Jun Ding, Tong-Mei Ding, Shuiyi Zhang, Yaqiu Wang, Feng Sha, Shu-Yu Zhang, Xin-Yan Wu e Qiong Li. "Cobalt-Catalyzed Ortho-C(sp2)–H Amidation of Benzaldehydes with Dioxazolones Using Transient Directing Groups". Organic Letters 21, n.º 18 (3 de setembro de 2019): 7342–45. http://dx.doi.org/10.1021/acs.orglett.9b02632.

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45

Dhiman, Ankit Kumar, Ankita Thakur, Inder Kumar, Rakesh Kumar e Upendra Sharma. "Co(III)-Catalyzed C–H Amidation of Nitrogen-Containing Heterocycles with Dioxazolones under Mild Conditions". Journal of Organic Chemistry 85, n.º 14 (19 de junho de 2020): 9244–54. http://dx.doi.org/10.1021/acs.joc.0c01237.

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46

Khan, Bhuttu, Vikas Dwivedi e Basker Sundararaju. "Cp*Co(III)‐Catalyzed o ‐Amidation of Benzaldehydes with Dioxazolones Using Transient Directing Group Strategy". Advanced Synthesis & Catalysis 362, n.º 5 (8 de janeiro de 2020): 1195–200. http://dx.doi.org/10.1002/adsc.201901267.

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47

Chalamet, Yvan, e Mohamed Taha. "In-line residence time distribution of dicarboxylic acid oligomers/dioxazoline chain extension by reactive extrusion". Polymer Engineering & Science 39, n.º 2 (fevereiro de 1999): 347–55. http://dx.doi.org/10.1002/pen.11421.

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48

Chalamet, Yvan, e Mohamed Taha. "Kinetic and rheokinetic study of dicarboxylic fatty acid chain extension using a dioxazoline coupling agent". Journal of Applied Polymer Science 74, n.º 4 (24 de outubro de 1999): 1017–24. http://dx.doi.org/10.1002/(sici)1097-4628(19991024)74:4<1017::aid-app29>3.0.co;2-y.

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49

Nan, Jiang, Pu Chen, Xue Gong, Yan Hu, Qiong Ma, Bo Wang e Yangmin Ma. "Metal-Free C–H [5 + 1] Carbonylation of 2-Alkenyl/Pyrrolylanilines Using Dioxazolones as Carbonylating Reagents". Organic Letters 23, n.º 9 (15 de abril de 2021): 3761–66. http://dx.doi.org/10.1021/acs.orglett.1c01147.

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50

Massouh, Joe, Antoine Petrelli, Virginie Bellière‐Baca, Damien Hérault e Hervé Clavier. "Rhodium(III)‐Catalyzed Aldehyde C−H Activation and Functionalization with Dioxazolones: An Entry to Imide Synthesis". Advanced Synthesis & Catalysis 364, n.º 4 (29 de dezembro de 2021): 831–37. http://dx.doi.org/10.1002/adsc.202101099.

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