Увійти

Готові списки джерел за темами / Dioxazolone / Статті в журналах

Статті в журналах з теми "Dioxazolone"

Щоб переглянути інші типи публікацій з цієї теми, перейдіть за посиланням: Dioxazolone.

Автор: Grafiati

Опубліковано: 19 жовтня 2024

Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями

Оберіть тип джерела:

Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Dioxazolone".

Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.

Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.

Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.

1

Borah, Gongutri, Preetismita Borah, and Pitambar Patel. "Cp*Co(iii)-catalyzed ortho-amidation of azobenzenes with dioxazolones." Organic & Biomolecular Chemistry 15, no. 18 (2017): 3854–59. http://dx.doi.org/10.1039/c7ob00540g.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

2

Zhang, Lei, Xiangyun Zheng, Jinkang Chen, Kang Cheng, Licheng Jin, Xinpeng Jiang, and Chuanming Yu. "Ru(ii)-Catalyzed C6-selective C–H amidation of 2-pyridones." Organic Chemistry Frontiers 5, no. 20 (2018): 2969–73. http://dx.doi.org/10.1039/c8qo00795k.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

3

Pan, Deng, Gen Luo, Yang Yu, Jimin Yang, and Yi Luo. "Computational insights into Ir(iii)-catalyzed allylic C–H amination of terminal alkenes: mechanism, regioselectivity, and catalytic activity." RSC Advances 11, no. 31 (2021): 19113–20. http://dx.doi.org/10.1039/d1ra03842g.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

4

Hall, David S., Toren Hynes, and J. R. Dahn. "Dioxazolone and Nitrile Sulfite Electrolyte Additives for Lithium-Ion Cells." Journal of The Electrochemical Society 165, no. 13 (2018): A2961—A2967. http://dx.doi.org/10.1149/2.0341813jes.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

5

Gauthier, Roby, David S. Hall, Katherine Lin, Jazmin Baltazar, Toren Hynes, and J. R. Dahn. "Impact of Functionalization and Co-Additives on Dioxazolone Electrolyte Additives." Journal of The Electrochemical Society 167, no. 8 (May 26, 2020): 080540. http://dx.doi.org/10.1149/1945-7111/ab8ed6.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

6

Ghosh, Payel, Sadhanendu Samanta, and Alakananda Hajra. "Rhodium(iii)-catalyzed ortho-C–H amidation of 2-arylindazoles with a dioxazolone as an amidating reagent." Organic & Biomolecular Chemistry 18, no. 9 (2020): 1728–32. http://dx.doi.org/10.1039/c9ob02756d.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

7

Hande, Akshay Ekanath, Nachimuthu Muniraj, and Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C-H Amidation of Azobenzene Derivatives Using Dioxazolone as an Amidating Reagent." ChemistrySelect 2, no. 21 (July 21, 2017): 5965–69. http://dx.doi.org/10.1002/slct.201701277.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

8

Hande, Akshay Ekanath, and 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, no. 24 (November 28, 2017): 13405–13. http://dx.doi.org/10.1021/acs.joc.7b02500.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

9

Liu, Chen-Fei, Man Liu, Jun-Shu Sun, Chao Li, and Lin Dong. "Synthesis of 2-aminobenzaldehydes by rhodium(iii)-catalyzed C–H amidation of aldehydes with dioxazolones." Organic Chemistry Frontiers 5, no. 13 (2018): 2115–19. http://dx.doi.org/10.1039/c8qo00413g.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

10

Tang, Shi-Biao, Xiao-Pan Fu, Gao-Rong Wu, Li-Li Zhang, Ke-Zuan Deng, Jin-Yue Yang, Cheng-Cai Xia, and Ya-Fei Ji. "Rhodium(iii)-catalyzed C4-amidation of indole-oximes with dioxazolones via C–H activation." Organic & Biomolecular Chemistry 18, no. 39 (2020): 7922–31. http://dx.doi.org/10.1039/d0ob01655a.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

11

Saxena, Paridhi, Neha Maida, and Manmohan Kapur. "Dioxazolones as masked ester surrogates in the Pd(ii)-catalyzed direct C–H arylation of 6,5-fused heterocycles." Chemical Communications 55, no. 75 (2019): 11187–90. http://dx.doi.org/10.1039/c9cc05563k.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

12

Wang, Jinlei, Guangfan Zheng, and Xingwei Li. "Rhodium(iii)-catalyzed diamidation of olefins via amidorhodation and further amidation." Chemical Communications 56, no. 56 (2020): 7809–12. http://dx.doi.org/10.1039/d0cc00952k.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

13

Liu, Yuan, Fang Xie, Ai-Qun Jia, and Xingwei Li. "Cp*Co(iii)-catalyzed amidation of olefinic and aryl C–H bonds: highly selective synthesis of enamides and pyrimidones." Chemical Communications 54, no. 34 (2018): 4345–48. http://dx.doi.org/10.1039/c8cc01447g.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

14

Song, Dan, Changfeng Huang, Peishi Liang, Baofu Zhu, Xiang Liu, and Hua Cao. "Lewis acid-catalyzed regioselective C–H carboxamidation of indolizines with dioxazolones via an acyl nitrene type rearrangement." Organic Chemistry Frontiers 8, no. 11 (2021): 2583–88. http://dx.doi.org/10.1039/d1qo00224d.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

15

Tobisch, Sven. "Copper hydride-mediated electrophilic amidation of vinylarenes with dioxazolones – a computational mechanistic study." Dalton Transactions 48, no. 38 (2019): 14337–46. http://dx.doi.org/10.1039/c9dt02540e.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

16

Ding, Jun, Wei Jiang, He-Yuan Bai, Tong-Mei Ding, Dafang Gao, Xiaoguang Bao, and 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, no. 64 (2018): 8889–92. http://dx.doi.org/10.1039/c8cc04904a.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

17

Bae, Hyeonwoong, Jinhwan Park, Rahyun Yoon, Seunghoon Lee, and Jongwoo Son. "Copper-catalyzed synthesis of primary amides through reductive N–O cleavage of dioxazolones." RSC Advances 14, no. 14 (2024): 9440–44. http://dx.doi.org/10.1039/d4ra00320a.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

18

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

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

19

Bondock, Samir, Ehab Abdel Latif та Johann Lex. "Solvent-free Photooxygenation of 5-methoxyoxazoles: Stereoselective Synthesis of α-amino-α-hydroxy Carboxylic Acid Derivatives". Journal of Chemical Research 2005, № 7 (липень 2005): 422–26. http://dx.doi.org/10.3184/030823405774309168.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

20

Pan, Jie, Haocong Li, Kai Sun, Shi Tang, and Bing Yu. "Visible-Light-Induced Decarboxylation of Dioxazolones to Phosphinimidic Amides and Ureas." Molecules 27, no. 12 (June 7, 2022): 3648. http://dx.doi.org/10.3390/molecules27123648.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

21

Colbeaux, Aimeline, Françoise Fenouillot, Jean-François Gerard, Mohamed Taha, and Henri Wautier. "Dioxazoline coupling of maleic anhydride modified polyethylene." Journal of Applied Polymer Science 97, no. 3 (2005): 837–43. http://dx.doi.org/10.1002/app.21793.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

22

Nishii, Yuji, Masahiro Miura, Chandrababu Naidu Kona, and Rikuto Oku. "Peri-Selective Direct Acylmethylation and Amidation of Naphthalene Derivatives Using Iridium and Rhodium Catalysts." Synthesis 53, no. 17 (March 31, 2021): 3126–36. http://dx.doi.org/10.1055/a-1472-1059.

Повний текст джерела

Анотація:

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.

Стилі APA, Harvard, Vancouver, ISO та ін.

23

Liao, Xian-Zhang, Man Liu, and Lin Dong. "An Approach to Vinylidenequinazolines from Isoxazoles and Dioxazolones." Journal of Organic Chemistry 87, no. 5 (January 28, 2022): 3741–50. http://dx.doi.org/10.1021/acs.joc.1c02746.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

24

van Vliet, Kaj M., and Bas de Bruin. "Dioxazolones: Stable Substrates for the Catalytic Transfer of Acyl Nitrenes." ACS Catalysis 10, no. 8 (March 30, 2020): 4751–69. http://dx.doi.org/10.1021/acscatal.0c00961.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

25

Samanta, Sadhanendu, Susmita Mondal, Debashis Ghosh, and Alakananda Hajra. "Rhodium-Catalyzed Directed C–H Amidation of Imidazoheterocycles with Dioxazolones." Organic Letters 21, no. 12 (June 12, 2019): 4905–9. http://dx.doi.org/10.1021/acs.orglett.9b01832.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

26

Mi, Xia, Weisheng Feng, Chao Pi, and Xiuling Cui. "Iridium(III)-Catalyzed C–H Amidation of Nitrones with Dioxazolones." Journal of Organic Chemistry 84, no. 9 (April 4, 2019): 5305–12. http://dx.doi.org/10.1021/acs.joc.9b00300.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

27

Chen, Jiajia, and Yuanzhi Xia. "Visible-Light-Induced Iron Catalysis for Nitrene Transfer Reactions with Dioxazolones." Chinese Journal of Organic Chemistry 41, no. 9 (2021): 3748. http://dx.doi.org/10.6023/cjoc202100069.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

28

Jeoung, Daeun, Kunyoung Kim, Sang Hoon Han, Prithwish Ghosh, Suk Hun Lee, Saegun Kim, Won An, Hyung Sik Kim, Neeraj Kumar Mishra, and In Su Kim. "Phthalazinone-Assisted C–H Amidation Using Dioxazolones Under Rh(III) Catalysis." Journal of Organic Chemistry 85, no. 11 (April 10, 2020): 7014–23. http://dx.doi.org/10.1021/acs.joc.0c00352.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

29

Huang, Yanzhen, Chao Pi, Zhen Tang, Yangjie Wu, and Xiuling Cui. "Cp*Co(III)-catalyzed C H amidation of azines with dioxazolones." Chinese Chemical Letters 31, no. 12 (December 2020): 3237–40. http://dx.doi.org/10.1016/j.cclet.2020.08.046.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

30

Chalamet, Yvan, and Mohamed Taha. "Carboxyl terminated polyamide 12 chain extension using a dioxazoline coupling agent." Journal of Polymer Science Part A: Polymer Chemistry 35, no. 17 (December 1997): 3697–705. http://dx.doi.org/10.1002/(sici)1099-0518(199712)35:17<3697::aid-pola9>3.0.co;2-p.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

31

Mishra, Neeraj Kumar, Yongguk Oh, Mijin Jeon, Sangil Han, Satyasheel Sharma, Sang Hoon Han, Sung Hee Um, and In Su Kim. "Site-Selective C-H Amidation of Azobenzenes with Dioxazolones under Rhodium Catalysis." European Journal of Organic Chemistry 2016, no. 29 (September 27, 2016): 4976–80. http://dx.doi.org/10.1002/ejoc.201601096.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

32

Tang, Jing‐Jing, Xiaoqiang Yu, Yi Wang, Yoshinori Yamamoto, and Ming Bao. "Interweaving Visible‐Light and Iron Catalysis for Nitrene Formation and Transformation with Dioxazolones." Angewandte Chemie 133, no. 30 (May 10, 2021): 16562–71. http://dx.doi.org/10.1002/ange.202016234.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

33

Tang, Jing‐Jing, Xiaoqiang Yu, Yi Wang, Yoshinori Yamamoto, and Ming Bao. "Interweaving Visible‐Light and Iron Catalysis for Nitrene Formation and Transformation with Dioxazolones." Angewandte Chemie International Edition 60, no. 30 (May 10, 2021): 16426–35. http://dx.doi.org/10.1002/anie.202016234.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

34

Han, Gi Uk, Seohyun Shin, Yonghyeon Baek, Dongwook Kim, Kooyeon Lee, Jeung Gon Kim, and Phil Ho Lee. "Mechanochemical Iridium(III)-Catalyzed B-Amidation of o-Carboranes with Dioxazolones." Organic Letters 23, no. 21 (October 18, 2021): 8622–27. http://dx.doi.org/10.1021/acs.orglett.1c03336.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

35

Jeon, Bomi, Uiseong Yeon, Jeong-Yu Son, and Phil Ho Lee. "Selective Rhodium-Catalyzed C–H Amidation of Azobenzenes with Dioxazolones under Mild Conditions." Organic Letters 18, no. 18 (August 26, 2016): 4610–13. http://dx.doi.org/10.1021/acs.orglett.6b02250.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

36

Chamni, Supakarn, Jinquan Zhang, and Hongbin Zou. "Benign synthesis of unsymmetrical arylurea derivatives using 3-substituted dioxazolones as isocyanate surrogates." Green Chemistry Letters and Reviews 13, no. 3 (July 2, 2020): 246–57. http://dx.doi.org/10.1080/17518253.2020.1807616.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

37

Wang, Xiaoyang, Song Song, and Ning Jiao. "Rh-catalyzed Transient Directing Group Promoted C-H Amidation of Benzaldehydes Utilizing Dioxazolones." Chinese Journal of Chemistry 36, no. 3 (January 11, 2018): 213–16. http://dx.doi.org/10.1002/cjoc.201700726.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

38

Guo, Wusheng, and Biwei Yan. "Recent Advances in Decarboxylative Conversions of Cyclic Carbonates and Beyond." Synthesis 54, no. 08 (December 7, 2021): 1964–76. http://dx.doi.org/10.1055/a-1715-7413.

Повний текст джерела

Анотація:

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

Стилі APA, Harvard, Vancouver, ISO та ін.

39

Sheng, Yaoguang, Jianmin Zhou, Yi Gao, Bingbing Duan, Yi Wang, Aleksandr Samorodov, Guang Liang, Qiuhua Zhao, and Zengqiang Song. "Ruthenium(II)-Catalyzed Direct C7-Selective Amidation of Indoles with Dioxazolones at Room Temperature." Journal of Organic Chemistry 86, no. 3 (January 20, 2021): 2827–39. http://dx.doi.org/10.1021/acs.joc.0c02779.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

40

Tang, Jing-Jing, Xiaoqiang Yu, Yoshinori Yamamoto, and Ming Bao. "Visible-Light-Promoted Iron-Catalyzed N-Arylation of Dioxazolones with Arylboronic Acids." ACS Catalysis 11, no. 22 (November 3, 2021): 13955–61. http://dx.doi.org/10.1021/acscatal.1c04538.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

41

Lee, Sumin, and Tomislav Rovis. "Rh(III)-Catalyzed Three-Component Syn-Carboamination of Alkenes Using Arylboronic Acids and Dioxazolones." ACS Catalysis 11, no. 14 (June 30, 2021): 8585–90. http://dx.doi.org/10.1021/acscatal.1c02406.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

42

Wang, Jie, Shanke Zha, Kehao Chen, Feifei Zhang, Chao Song, and Jin Zhu. "Quinazoline Synthesis via Rh(III)-Catalyzed Intermolecular C–H Functionalization of Benzimidates with Dioxazolones." Organic Letters 18, no. 9 (April 8, 2016): 2062–65. http://dx.doi.org/10.1021/acs.orglett.6b00691.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

43

Schroth, Werner, and Olaf Peters. "2-Acylmethyl-1, 3, 4-dioxazole durch Ketovinylierung von Hydroxamsäuren." Zeitschrift für Chemie 18, no. 2 (September 1, 2010): 57–58. http://dx.doi.org/10.1002/zfch.19780180204.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

44

Huang, Jie, Jun Ding, Tong-Mei Ding, Shuiyi Zhang, Yaqiu Wang, Feng Sha, Shu-Yu Zhang, Xin-Yan Wu, and Qiong Li. "Cobalt-Catalyzed Ortho-C(sp2)–H Amidation of Benzaldehydes with Dioxazolones Using Transient Directing Groups." Organic Letters 21, no. 18 (September 3, 2019): 7342–45. http://dx.doi.org/10.1021/acs.orglett.9b02632.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

45

Dhiman, Ankit Kumar, Ankita Thakur, Inder Kumar, Rakesh Kumar, and Upendra Sharma. "Co(III)-Catalyzed C–H Amidation of Nitrogen-Containing Heterocycles with Dioxazolones under Mild Conditions." Journal of Organic Chemistry 85, no. 14 (June 19, 2020): 9244–54. http://dx.doi.org/10.1021/acs.joc.0c01237.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

46

Khan, Bhuttu, Vikas Dwivedi, and Basker Sundararaju. "Cp*Co(III)‐Catalyzed o ‐Amidation of Benzaldehydes with Dioxazolones Using Transient Directing Group Strategy." Advanced Synthesis & Catalysis 362, no. 5 (January 8, 2020): 1195–200. http://dx.doi.org/10.1002/adsc.201901267.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

47

Chalamet, Yvan, and Mohamed Taha. "In-line residence time distribution of dicarboxylic acid oligomers/dioxazoline chain extension by reactive extrusion." Polymer Engineering & Science 39, no. 2 (February 1999): 347–55. http://dx.doi.org/10.1002/pen.11421.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

48

Chalamet, Yvan, and Mohamed Taha. "Kinetic and rheokinetic study of dicarboxylic fatty acid chain extension using a dioxazoline coupling agent." Journal of Applied Polymer Science 74, no. 4 (October 24, 1999): 1017–24. http://dx.doi.org/10.1002/(sici)1097-4628(19991024)74:4<1017::aid-app29>3.0.co;2-y.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

49

Nan, Jiang, Pu Chen, Xue Gong, Yan Hu, Qiong Ma, Bo Wang, and Yangmin Ma. "Metal-Free C–H [5 + 1] Carbonylation of 2-Alkenyl/Pyrrolylanilines Using Dioxazolones as Carbonylating Reagents." Organic Letters 23, no. 9 (April 15, 2021): 3761–66. http://dx.doi.org/10.1021/acs.orglett.1c01147.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

50

Massouh, Joe, Antoine Petrelli, Virginie Bellière‐Baca, Damien Hérault, and Hervé Clavier. "Rhodium(III)‐Catalyzed Aldehyde C−H Activation and Functionalization with Dioxazolones: An Entry to Imide Synthesis." Advanced Synthesis & Catalysis 364, no. 4 (December 29, 2021): 831–37. http://dx.doi.org/10.1002/adsc.202101099.

Повний текст джерела

Стилі APA, Harvard, Vancouver, ISO та ін.

Ми пропонуємо знижки на всі преміум-плани для авторів, чиї праці увійшли до тематичних добірок літератури. Зв'яжіться з нами, щоб отримати унікальний промокод!