Статті в журналах з теми "C–H Bond - Maleimides"
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He, Qiyuan, Yusuke Ano, and Naoto Chatani. "The Pd-catalyzed C–H alkylation of ortho-methyl-substituted aromatic amides with maleimide occurs preferentially at the ortho-methyl C–H bond over the ortho-C–H bond." Chemical Communications 55, no. 67 (2019): 9983–86. http://dx.doi.org/10.1039/c9cc05321b.
Повний текст джерелаZhao, Sheng-Yin, Hong-Ru Tan, Lun Wang, Jia-Nan Zhu, and Zhen-Hua Yang. "Iodine-Promoted C(sp 2)–H Thiolation of Maleimides with Dimethyl Sulfoxide and Thiols." Synthesis 50, no. 20 (July 30, 2018): 4113–23. http://dx.doi.org/10.1055/s-0037-1609585.
Повний текст джерелаPan, Changduo, Yun Wang, Chao Wu, and Jin-Tao Yu. "Rhodium-catalyzed C7-alkylation of indolines with maleimides." Organic & Biomolecular Chemistry 16, no. 5 (2018): 693–97. http://dx.doi.org/10.1039/c7ob03039h.
Повний текст джерелаJeganmohan, Masilamani, Meledath Sudhakaran Keerthana, and Ramasamy Manoharan. "Cobalt(III)-Catalyzed Redox-Neutral Coupling of Acrylamides with Activated Alkenes via C–H Bond Activation." Synthesis 52, no. 11 (March 30, 2020): 1625–33. http://dx.doi.org/10.1055/s-0039-1690866.
Повний текст джерелаSun, Meng, Xiang-Xiang Chen, Jiang-Tao Ren, Jing-Lei Xu, Hu Xie, Wei Sun, and Ya-Min Li. "Cobalt(III)-Catalyzed 1,4-Addition of C(sp3)–H Bonds to Maleimides." Synlett 29, no. 12 (May 29, 2018): 1601–6. http://dx.doi.org/10.1055/s-0037-1609847.
Повний текст джерелаBettadapur, Kiran R., Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "A deciduous directing group approach for the addition of aryl and vinyl nucleophiles to maleimides." Chemical Communications 53, no. 46 (2017): 6251–54. http://dx.doi.org/10.1039/c7cc02392h.
Повний текст джерелаZhao, Sheng-Yin, Zhen-Hua Yang, Jia-Nan Zhu, Ze-Hui Jin, and Jian Zheng. "Copper-Catalyzed Intermolecular Thioamination of Maleimides with Thiols and Formamides: A One-Step Construction of 3-Amino-4-thiomaleimides Using Formamides as Nitrogen Sources." Synthesis 50, no. 23 (August 7, 2018): 4627–36. http://dx.doi.org/10.1055/s-0037-1610536.
Повний текст джерелаChen, Xiangxiang, Jiangtao Ren, Hu Xie, Wei Sun, Meng Sun, and Biao Wu. "Cobalt(iii)-catalyzed 1,4-addition of C–H bonds of oximes to maleimides." Organic Chemistry Frontiers 5, no. 2 (2018): 184–88. http://dx.doi.org/10.1039/c7qo00687j.
Повний текст джерелаMangialetto, Jessica, Kiano Gorissen, Lise Vermeersch, Bruno Van Mele, Niko Van den Brande, and Freija De Vleeschouwer. "Hydrogen-Bond-Assisted Diels–Alder Kinetics or Self-Healing in Reversible Polymer Networks? A Combined Experimental and Theoretical Study." Molecules 27, no. 6 (March 17, 2022): 1961. http://dx.doi.org/10.3390/molecules27061961.
Повний текст джерелаMuniraj, Nachimuthu, and Kandikere Ramaiah Prabhu. "Cobalt(III)-Catalyzed C–H Activation: Azo Directed Selective 1,4-Addition of Ortho C–H Bond to Maleimides." Journal of Organic Chemistry 82, no. 13 (June 19, 2017): 6913–21. http://dx.doi.org/10.1021/acs.joc.7b01094.
Повний текст джерелаKeshri, Puspam, Kiran R. Bettadapur, Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "Ru(II)-Catalyzed C–H Activation: Amide-Directed 1,4-Addition of the Ortho C–H Bond to Maleimides." Journal of Organic Chemistry 81, no. 14 (July 7, 2016): 6056–65. http://dx.doi.org/10.1021/acs.joc.6b01160.
Повний текст джерелаBettadapur, Kiran R., Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "Ru (II)-Catalyzed C–H Activation: Ketone-Directed Novel 1,4-Addition of Ortho C–H Bond to Maleimides." Organic Letters 17, no. 19 (September 8, 2015): 4658–61. http://dx.doi.org/10.1021/acs.orglett.5b01810.
Повний текст джерелаLi, Hongji, Wenjie Zhang, Xueyan Liu, and Zhenfeng Tian. "Rh(III)-Catalyzed Olefination and Alkylation of Arenes with Maleimides: A Tunable Strategy for C(sp2)–H Functionalization." Synthesis 53, no. 13 (February 15, 2021): 2229–39. http://dx.doi.org/10.1055/s-0037-1610765.
Повний текст джерелаLiang, Zhongwei, Song Xu, Wenyan Tian, and Ronghua Zhang. "Eosin Y-catalyzed visible-light-mediated aerobic oxidative cyclization of N,N-dimethylanilines with maleimides." Beilstein Journal of Organic Chemistry 11 (April 1, 2015): 425–30. http://dx.doi.org/10.3762/bjoc.11.48.
Повний текст джерелаBettadapur, Kiran R., Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "ChemInform Abstract: Ru(II)-Catalyzed C-H Activation: Ketone-Directed Novel 1,4-Addition of ortho C-H Bond to Maleimides." ChemInform 47, no. 9 (February 2016): no. http://dx.doi.org/10.1002/chin.201609060.
Повний текст джерелаOhara, Nozomi, Supriya Rej, and Naoto Chatani. "Rh(I)-catalyzed Addition of the ortho C-H Bond in Aryl Sulfonamides to Maleimides." Chemistry Letters 49, no. 9 (September 5, 2020): 1053–57. http://dx.doi.org/10.1246/cl.200353.
Повний текст джерелаReddy, Keesari N., Medikonda V. Krishna Rao, Balasubramanian Sridhar, and Basi V. Subba Reddy. "Ru(II)‐Catalyzed Hydroarylation of Maleimides with Cyclic N ‐SulfonylKetimines through ortho ‐C‐H Bond Activation." ChemistrySelect 3, no. 18 (May 14, 2018): 5062–65. http://dx.doi.org/10.1002/slct.201800352.
Повний текст джерелаYuan, Yu-Chao, Marion Goujon, Christian Bruneau, Thierry Roisnel, and Rafael Gramage-Doria. "C–H Bond Alkylation of Cyclic Amides with Maleimides via a Site-Selective-Determining Six-Membered Ruthenacycle." Journal of Organic Chemistry 84, no. 24 (November 25, 2019): 16183–91. http://dx.doi.org/10.1021/acs.joc.9b02690.
Повний текст джерелаManoharan, Ramasamy, and Masilamani Jeganmohan. "Alkylation, Annulation, and Alkenylation of Organic Molecules with Maleimides by Transition‐Metal‐Catalyzed C‐H Bond Activation." Asian Journal of Organic Chemistry 8, no. 11 (May 10, 2019): 1949–69. http://dx.doi.org/10.1002/ajoc.201900054.
Повний текст джерелаCheng, Xiaoyu, Baojun Li, Mengsi Zhang, Haotian Lu, Wenbo Wang, Yun Ding, and Aiguo Hu. "Direct functionalization of cyclic ethers with maleimide iodides via free radial-mediated sp3 C–H activation." Chemical Communications 57, no. 39 (2021): 4787–90. http://dx.doi.org/10.1039/d1cc01484f.
Повний текст джерелаHe, Qiyuan, Takuma Yamaguchi, and Naoto Chatani. "Rh(I)-Catalyzed Alkylation of ortho-C–H Bonds in Aromatic Amides with Maleimides." Organic Letters 19, no. 17 (August 11, 2017): 4544–47. http://dx.doi.org/10.1021/acs.orglett.7b02135.
Повний текст джерелаKumar, Rakesh, Rohit Kumar, Devesh Chandra, and Upendra Sharma. "Cp*CoIII–Catalyzed Alkylation of Primary and Secondary C(sp3)-H Bonds of 8-Alkylquinolines with Maleimides." Journal of Organic Chemistry 84, no. 3 (January 8, 2019): 1542–52. http://dx.doi.org/10.1021/acs.joc.8b02974.
Повний текст джерелаWang, Bing, James F. Hinton, and Peter Pulay. "C−H···O Hydrogen Bond betweenN-Methyl Maleimide and Dimethyl Sulfoxide: A Combined NMR and Ab Initio Study." Journal of Physical Chemistry A 107, no. 23 (June 2003): 4683–87. http://dx.doi.org/10.1021/jp026986b.
Повний текст джерелаGurram, Ravi Kumar, Manda Rajesh, Maneesh Kumar Reddy Singam, Jagadeesh Babu Nanubolu, and Maddi Sridhar Reddy. "A Sequential Activation of Alkyne and C–H Bonds for the Tandem Cyclization and Annulation of Alkynols and Maleimides through Cooperative Sc(III) and Cp*-Free Co(II) Catalysis." Organic Letters 22, no. 14 (July 7, 2020): 5326–30. http://dx.doi.org/10.1021/acs.orglett.0c01533.
Повний текст джерелаGurram, Ravi Kumar, Manda Rajesh, Maneesh Kumar Reddy Singam, Jagadeesh Babu Nanubolu, and Maddi Sridhar Reddy. "Correction to “A Sequential Activation of Alkyne and C–H Bonds for the Tandem Cyclization and Annulation of Alkynols and Maleimides through Cooperative Sc(III) and Cp*-Free Co(II) Catalysis”." Organic Letters 22, no. 18 (September 8, 2020): 7408. http://dx.doi.org/10.1021/acs.orglett.0c02807.
Повний текст джерелаBulatov, Evgeny, Dina Boyarskaya, Tatiana Chulkova, and Matti Haukka. "2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate." Acta Crystallographica Section E Structure Reports Online 70, no. 3 (February 8, 2014): o260. http://dx.doi.org/10.1107/s1600536814002372.
Повний текст джерелаTian, Ting, An-Shun Dong, Dan Chen, Xian-Ting Cao, and Guannan Wang. "Regioselective C–C cross-coupling of 1,2,4-thiadiazoles with maleimides through iridium-catalyzed C–H activation." Organic & Biomolecular Chemistry 17, no. 33 (2019): 7664–68. http://dx.doi.org/10.1039/c9ob01539f.
Повний текст джерелаSchapin, Igor Yu, and Vladimir S. Mastryukov. "Inverse “bond length/bond angle” relationship: CH versus HCH." Journal of Molecular Structure 268, no. 1-3 (April 1992): 307–10. http://dx.doi.org/10.1016/0022-2860(92)85079-v.
Повний текст джерелаPark, Hyunjin, Jineun Kim, Eunjin Kwon, and Tae Ho Kim. "Crystal structure of flumioxazin." Acta Crystallographica Section E Crystallographic Communications 71, no. 10 (September 17, 2015): o768. http://dx.doi.org/10.1107/s2056989015017223.
Повний текст джерелаSaid, Awad I., and Talaat I. El-Emary. "Diastereoselective synthesis of atropisomeric pyrazolyl pyrrolo[3,4-d]isoxazolidines via pyrazolyl nitrone cycloaddition to facially divergent maleimides: intensive NMR and DFT studies." RSC Advances 10, no. 2 (2020): 845–50. http://dx.doi.org/10.1039/c9ra10039c.
Повний текст джерелаHirata, Toshifumi, Asuka Takarada, Mohamed-Elamir F. Hegazy, Yuya Sato, Akihito Matsushima, Yoko Kondo, Ayako Matsuki, and Hiroki Hamada. "Hydrogenation of the C–C double bond of maleimides with cultured plant cells." Journal of Molecular Catalysis B: Enzymatic 32, no. 4 (February 2005): 131–34. http://dx.doi.org/10.1016/j.molcatb.2004.11.008.
Повний текст джерелаPi, Chao, Yaping Qu, Xiuling Cui, and Yangjie Wu. "Silver-Catalyzed C—H Alkylation of 2-Arylindoles with Maleimides." Chinese Journal of Organic Chemistry 40, no. 3 (2020): 740. http://dx.doi.org/10.6023/cjoc201907040.
Повний текст джерелаLi, Bang, Qi Mao, Jia Zhou, Feng Liu, and Na Ye. "HFIP-promoted Michael reactions: direct para-selective C–H activation of anilines with maleimides." Organic & Biomolecular Chemistry 17, no. 8 (2019): 2242–46. http://dx.doi.org/10.1039/c8ob03073a.
Повний текст джерелаDavies, H. M. L., and D. Morton. "ChemInform Abstract: C-C Bond Formation by C-H Bond Activation." ChemInform 42, no. 42 (September 27, 2011): no. http://dx.doi.org/10.1002/chin.201142249.
Повний текст джерелаJing, Hua-Qing, Jon C. Antilla, and Hong-Liang Li. "Regioselective C-H Borylation of C (sp2)-H Bond." Madridge Journal of Novel Drug Research 3, no. 1 (February 26, 2019): 114–19. http://dx.doi.org/10.18689/mjndr-1000117.
Повний текст джерелаZhao, Hua, Taimin Wang, Zhineng Qing, and Hongbin Zhai. "Cobalt-catalyzed 2-(1-methylhydrazinyl)pyridine-assisted cyclization of thiophene-2-carbohydrazides with maleimides: efficient synthesis of thiophene-fused pyridones." Chemical Communications 56, no. 41 (2020): 5524–27. http://dx.doi.org/10.1039/d0cc01582b.
Повний текст джерелаGhosh, Asim Kumar, Sadhanendu Samanta, Payel Ghosh, Sukanya Neogi, and Alakananda Hajra. "Regioselective hydroarylation and arylation of maleimides with indazoles via a Rh(iii)-catalyzed C–H activation." Organic & Biomolecular Chemistry 18, no. 16 (2020): 3093–97. http://dx.doi.org/10.1039/d0ob00353k.
Повний текст джерелаWILSON, ELIZABETH K. "EXPLAINING C-H BOND STRENGTHS." Chemical & Engineering News 84, no. 10 (March 6, 2006): 65. http://dx.doi.org/10.1021/cen-v084n010.p065.
Повний текст джерелаMeng, Guangrong, and Michal Szostak. "Rhodium-Catalyzed C–H Bond Functionalization with Amides by Double C–H/C–N Bond Activation." Organic Letters 18, no. 4 (February 8, 2016): 796–99. http://dx.doi.org/10.1021/acs.orglett.6b00058.
Повний текст джерелаZhao, Hua, Xiaoru Shao, Taimin Wang, Shengxian Zhai, Shuxian Qiu, Cheng Tao, Huifei Wang, and Hongbin Zhai. "A 2-(1-methylhydrazinyl)pyridine-directed C–H functionalization/spirocyclization cascade: facile access to spirosuccinimide derivatives." Chemical Communications 54, no. 39 (2018): 4927–30. http://dx.doi.org/10.1039/c8cc01774c.
Повний текст джерелаBettadapur, Kiran R., Mahadev Sharanappa Sherikar, Veeranjaneyulu Lanke, and Kandikere Ramaiah Prabhu. "RhIII -Catalyzed C−H Activation: Mizoroki-Heck-Type Reaction of Maleimides." Asian Journal of Organic Chemistry 7, no. 7 (May 30, 2018): 1338–42. http://dx.doi.org/10.1002/ajoc.201800193.
Повний текст джерелаSharma, Satyasheel, Sang Hoon Han, Hyeim Jo, Sangil Han, Neeraj Kumar Mishra, Miji Choi, Taejoo Jeong, Jihye Park, and In Su Kim. "Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides." European Journal of Organic Chemistry 2016, no. 21 (June 24, 2016): 3611–18. http://dx.doi.org/10.1002/ejoc.201600558.
Повний текст джерелаNarayan, Rishikesh, Kiran Matcha, and Andrey P. Antonchick. "Metal-Free Oxidative CC Bond Formation through CH Bond Functionalization." Chemistry - A European Journal 21, no. 42 (August 3, 2015): 14678–93. http://dx.doi.org/10.1002/chem.201502005.
Повний текст джерелаZheng, Qing-Zhong, and Ning Jiao. "Ag-catalyzed C–H/C–C bond functionalization." Chemical Society Reviews 45, no. 16 (2016): 4590–627. http://dx.doi.org/10.1039/c6cs00107f.
Повний текст джерелаCubbage, Kara L, Andrew J Orr-Ewing, and Kevin I Booker-Milburn. "First Higher-Order Photocycloaddition to a CN Bond: 1,3-Diazepines from Maleimides." Angewandte Chemie International Edition 48, no. 14 (March 23, 2009): 2514–17. http://dx.doi.org/10.1002/anie.200805846.
Повний текст джерелаCubbage, Kara L, Andrew J Orr-Ewing, and Kevin I Booker-Milburn. "First Higher-Order Photocycloaddition to a CN Bond: 1,3-Diazepines from Maleimides." Angewandte Chemie 121, no. 14 (March 23, 2009): 2552–55. http://dx.doi.org/10.1002/ange.200805846.
Повний текст джерелаZhao, Yating, and Wujiong Xia. "Photochemical C–H bond coupling for (hetero)aryl C(sp2)–C(sp3) bond construction." Organic & Biomolecular Chemistry 17, no. 20 (2019): 4951–63. http://dx.doi.org/10.1039/c9ob00244h.
Повний текст джерелаWang, Xiao, Ming-Zhu Lu, and Teck-Peng Loh. "Transition-Metal-Catalyzed C–C Bond Macrocyclization via Intramolecular C–H Bond Activation." Catalysts 13, no. 2 (February 17, 2023): 438. http://dx.doi.org/10.3390/catal13020438.
Повний текст джерелаPing, Yuanyuan, Qiuping Ding, and Yiyuan Peng. "Advances in C–CN Bond Formation via C–H Bond Activation." ACS Catalysis 6, no. 9 (August 10, 2016): 5989–6005. http://dx.doi.org/10.1021/acscatal.6b01632.
Повний текст джерелаEsteruelas, Miguel A., Montserrat Oliván, and Andrea Vélez. "POP–Rhodium-Promoted C–H and B–H Bond Activation and C–B Bond Formation." Organometallics 34, no. 10 (May 2015): 1911–24. http://dx.doi.org/10.1021/acs.organomet.5b00176.
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