Статті в журналах з теми "Facile Michael Addition Reaction"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Facile Michael Addition Reaction".
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.
Reddy, S. Madhava, and H. M. Walborsky. "A facile intramolecular Michael addition reaction." Journal of Organic Chemistry 51, no. 13 (June 1986): 2605–7. http://dx.doi.org/10.1021/jo00363a042.
Повний текст джерелаStepanova, Ekaterina, Andrey Maslivets, Svetlana Kasatkina, and Maksim Dmitriev. "Diversity-Oriented Synthesis via Catalyst-Free Addition of Ketones to [e]-Fused 1H-Pyrrole-2,3-diones." Synthesis 50, no. 24 (August 20, 2018): 4897–904. http://dx.doi.org/10.1055/s-0037-1610647.
Повний текст джерелаWang, Yi-Fan, Cheng-Yu He, Longlei Hou, Ping Tian, Guo-Qiang Lin та Xiaofeng Tong. "Facile Access to 1,5-Benzodiazepines via Amine-Promoted (4+3) Annulations of δ-Acetoxy Allenoates with o-Diaminobenzenes under Mild Conditions". Synlett 29, № 09 (23 березня 2018): 1176–80. http://dx.doi.org/10.1055/s-0037-1609347.
Повний текст джерелаYang, Jingya, Tianyuan Li, Hongyan Zhou, Nana Li, Dongtai Xie, and Zheng Li. "Potassium Hydroxide Catalysed Intermolecular Aza-Michael Addition of 3-Cyanoindole to Aromatic Enones." Synlett 28, no. 10 (February 28, 2017): 1227–31. http://dx.doi.org/10.1055/s-0036-1588152.
Повний текст джерелаTerent'ev, Alexander O., Vera A. Vil', Ivan A. Yaremenko, Oleg V. Bityukov, Dmitri O. Levitsky, Vladimir V. Chernyshev, Gennady I. Nikishin та Fabrice Fleury. "Preparation of a microsized cerium chloride-based catalyst and its application in the Michael addition of β-diketones to vinyl ketones". New J. Chem. 38, № 4 (2014): 1493–502. http://dx.doi.org/10.1039/c3nj01454a.
Повний текст джерелаBoruah, Romesh C., Anil Saikia, Apurba Chetia, and Utpal Bora. "A Facile Synthesis of 1,6-Diketonesvia a Three-Component Michael Addition Reaction." Synlett, no. 10 (2003): 1506–8. http://dx.doi.org/10.1055/s-2003-40821.
Повний текст джерелаRulev, Alexander Yu, Alexey R. Romanov, Alexander V. Popov, Evgeniy V. Kondrashov, and Sergey V. Zinchenko. "Reaction of Bromoenones with Amidines: A Simple Catalyst-Free Approach to Trifluoromethylated Pyrimidines." Synthesis 52, no. 10 (March 9, 2020): 1512–22. http://dx.doi.org/10.1055/s-0040-1707969.
Повний текст джерелаLin, Ning, Qiu-Xiang Wei, Li-Hua Jiang, Yan-Qiu Deng, Zhen-Wei Zhang, and Qing Chen. "Asymmetric Michael Addition of Malononitrile with Chalcones via Rosin-Derived Bifunctional Squaramide." Catalysts 10, no. 1 (December 20, 2019): 14. http://dx.doi.org/10.3390/catal10010014.
Повний текст джерелаGuy Taylor, Jason, Wellington Martins Ventura, and Luiz Guilherme Souza de Assis. "Facile Synthesis of Indolines by a Tandem Nitro-reduction Aza Michael Addition Reaction." HETEROCYCLES 87, no. 10 (2013): 2023. http://dx.doi.org/10.3987/com-13-12789.
Повний текст джерелаFustero, Santos, Javier Moscardó, María Sánchez-Roselló, Elsa Rodríguez, and Pablo Barrio. "Tandem Nucleophilic Addition−Intramolecular Aza-Michael Reaction: Facile Synthesis of Chiral Fluorinated Isoindolines." Organic Letters 12, no. 23 (December 3, 2010): 5494–97. http://dx.doi.org/10.1021/ol102341n.
Повний текст джерелаGuo, Shengmei, Kun Jie, Ling Huang, Zhebin Zhang, Yufeng Wang, Zhengjiang Fu, and Hu Cai. "Fe-Catalyzed Bisphosphorylation of Amino-2-en-1-ones with Trialkyl Phosphites." Synlett 30, no. 09 (April 18, 2019): 1090–94. http://dx.doi.org/10.1055/s-0037-1611803.
Повний текст джерелаCui, Dong-Xiao, Yue-Dan Li, Jun-Chao Zhu, Yan-Yan Jia, Ai-Dong Wen, and Ping-An Wang. "Highly Efficient Michael Reactions of Nitroolefins by Grinding Means." Current Organic Synthesis 16, no. 3 (June 17, 2019): 449–57. http://dx.doi.org/10.2174/1570179416666190101122150.
Повний текст джерелаAn, Litao, Xiaojun Sun, Meng Lv, Jianfeng Zhou, Fengxia Zhu, and Hui Zhong. "Metal-free oxidative coupling of aminopyridines with nitroolefins to imidazo[1,2-a]pyridine in the presence of I2–TBHP–pyridine." Zeitschrift für Naturforschung B 71, no. 2 (February 1, 2016): 141–47. http://dx.doi.org/10.1515/znb-2015-0171.
Повний текст джерелаDu, Yuqun, Hongxia Yan, Song Niu, Lihua Bai, and Fu Chai. "Facile one-pot synthesis of novel water-soluble fluorescent hyperbranched poly(amino esters)." RSC Advances 6, no. 91 (2016): 88030–37. http://dx.doi.org/10.1039/c6ra19062f.
Повний текст джерелаYang, Guang, Wei Long, Wenfeng Yan, Hongye Huang, Meiying Liu, Hui Ouyang, Yulin Feng, Liangji Liu, Xiaoyong Zhang, and Yen Wei. "Surface PEGylation of nanodiamond through a facile Michael addition reaction for intracellular drug delivery." Journal of Drug Delivery Science and Technology 57 (June 2020): 101644. http://dx.doi.org/10.1016/j.jddst.2020.101644.
Повний текст джерелаChen, Bo, and Shengming Ma. "Tandem Michael Addition/Cyclization Reaction of 2,3-Allenoates with Organozincs: Facile Synthesis of Isocoumarins." Organic Letters 15, no. 15 (July 22, 2013): 3884–87. http://dx.doi.org/10.1021/ol401625t.
Повний текст джерелаAhmed, Naseem, and Iram Parveen. "A Route to Highly Functionalized Stereospecific trans-Aminated Aurones from 3-Bromoflavones with Aniline and N-Phenylurea via a Domino Aza-Michael Ring Opening and Cyclization Reactions." Synthesis 51, no. 04 (October 10, 2018): 960–70. http://dx.doi.org/10.1055/s-0037-1610662.
Повний текст джерелаLiao, Jia-Yu, Wei Jie Yap, Ji'En Wu, Ming Wah Wong, and Yu Zhao. "Three-component reactions of isocyanoacetates, amines and 3-formylchromones initiated by an unexpected aza-Michael addition." Chemical Communications 53, no. 65 (2017): 9067–70. http://dx.doi.org/10.1039/c7cc03468g.
Повний текст джерелаChen, Zhen-Zhen, Dong-Zhao Yang, Ying-Ying Dong, Mei Chi, Shou-Zhi Pu та Qi Sun. "Hf(OTf)4-Catalyzed Three-Component Synthesis of N-Carbamate-Protected β-Amino Ketones". Molecules 27, № 3 (8 лютого 2022): 1122. http://dx.doi.org/10.3390/molecules27031122.
Повний текст джерелаRather, Adil Majeed, and Uttam Manna. "Stretchable and durable superhydrophobicity that acts both in air and under oil." Journal of Materials Chemistry A 5, no. 29 (2017): 15208–16. http://dx.doi.org/10.1039/c7ta04073c.
Повний текст джерелаChittimalla, Santhosh, Chennakesavulu Bandi, Vinod Gadi, and Siva Gunturu. "Facile Synthesis of 2-Arylindoles through Plancher-Type Rearrangement of 3-Alkyl-3-Arylindolenines." Synlett 28, no. 15 (July 5, 2017): 1994–99. http://dx.doi.org/10.1055/s-0036-1588448.
Повний текст джерелаYao, Wei, Mingtai Sun, Yuannian Zhang, Hui Yang, Dong Liang, Haixia Wu, Runyan Ni, Ming Wah Wong, and Dejian Huang. "Photo-induced C–H bond activation of N,N′-dialkylethylenediamine upon aza-Michael addition to 1,8-pyrenedione: facile synthesis of fluorescent pyrene derivatives." Organic Chemistry Frontiers 5, no. 10 (2018): 1679–83. http://dx.doi.org/10.1039/c8qo00183a.
Повний текст джерелаTeimouri, Mohammad Bagher, та Tayyebeh Abbasi. "Facile synthesis of oxaspirobicyclic butenolides via a domino Michael addition/aldol reaction/γ-lactonization sequence". Tetrahedron 66, № 21 (травень 2010): 3795–800. http://dx.doi.org/10.1016/j.tet.2010.03.058.
Повний текст джерелаVentura, Wellington Martins, Luiz Guilherme Souza de Assis, and Jason Guy Taylor. "ChemInform Abstract: Facile Synthesis of Indolines by a Tandem Nitro-Reduction Aza Michael Addition Reaction." ChemInform 45, no. 9 (February 14, 2014): no. http://dx.doi.org/10.1002/chin.201409128.
Повний текст джерелаFustero, Santos, Javier Moscardo, Maria Sanchez-Rosello, Elsa Rodriguez, and Pablo Barrio. "ChemInform Abstract: Tandem Nucleophilic Addition-Intramolecular Aza-Michael Reaction: Facile Synthesis of Chiral Fluorinated Isoindolines." ChemInform 42, no. 12 (February 24, 2011): no. http://dx.doi.org/10.1002/chin.201112110.
Повний текст джерелаSuriyakala, Tevaraj, Alagiri Chinnaraj, Velmurugan Senthilkumar, Mohamedsulaiman Kamal Nasar та Gurusamy Ravindran. "Regioselective Synthesis and Antibacterial Studies of α,β-Unsaturated Ketone Substituted Cyclohexanols via Tandem Michael Addition-Aldol Addition-Cyclization Sequence under Solvent-Free Conditions". Asian Journal of Chemistry 34, № 10 (2022): 2646–50. http://dx.doi.org/10.14233/ajchem.2022.23907.
Повний текст джерелаFu, Hao, Linbo Gong, and Shuling Gong. "A New Approach Utilizing Aza-Michael Addition for Hydrolysis-Resistance Non-Ionic Waterborne Polyester." Polymers 14, no. 13 (June 29, 2022): 2655. http://dx.doi.org/10.3390/polym14132655.
Повний текст джерелаPal, Rammohan, Arpita Das Gupta та Asok K. Mallik. "Facile Iodine-Catalyzed Michael Addition of Indoles to α,α′-Bis(arylmethylene)cyclopentanones: An Efficient Synthesis of E-2-(3-Indolylphenylmethyl)-5-phenylmethylenecyclopentanones". ISRN Organic Chemistry 2012 (28 листопада 2012): 1–6. http://dx.doi.org/10.5402/2012/674629.
Повний текст джерелаGobbo, Pierangelo, Mark C. Biesinger, and Mark S. Workentin. "Facile synthesis of gold nanoparticle (AuNP)–carbon nanotube (CNT) hybrids through an interfacial Michael addition reaction." Chemical Communications 49, no. 27 (2013): 2831. http://dx.doi.org/10.1039/c3cc00050h.
Повний текст джерелаChen, Bo, and Shengming Ma. "ChemInform Abstract: Tandem Michael Addition/Cyclization Reaction of 2,3-Allenoates with Organozincs: Facile Synthesis of Isocoumarins." ChemInform 44, no. 51 (December 2, 2013): no. http://dx.doi.org/10.1002/chin.201351165.
Повний текст джерелаSun, Yanping, Hui Liu, Lin Cheng, Shimeng Zhu, Cuifang Cai, Tianzhi Yang, Li Yang, and Pingtian Ding. "Thiol Michael addition reaction: a facile tool for introducing peptides into polymer-based gene delivery systems." Polymer International 67, no. 1 (November 27, 2017): 25–31. http://dx.doi.org/10.1002/pi.5490.
Повний текст джерелаChetia, Apurba, Chandan J. Saikia, Kushal C. Lekhok, and Romesh C. Boruah. "A facile synthesis of 1,7-dicarbonyl compounds via three-component Michael addition reactions." Tetrahedron Letters 45, no. 12 (March 2004): 2649–51. http://dx.doi.org/10.1016/j.tetlet.2004.01.137.
Повний текст джерелаLin, Hui, Junjie Ou, Zhongshan Liu, Hongwei Wang, Jing Dong, and Hanfa Zou. "Facile construction of macroporous hybrid monoliths via thiol-methacrylate Michael addition click reaction for capillary liquid chromatography." Journal of Chromatography A 1379 (January 2015): 34–42. http://dx.doi.org/10.1016/j.chroma.2014.12.031.
Повний текст джерелаTeimouri, Mohammad Bagher, та Tayyebeh Abbasi. "ChemInform Abstract: Facile Synthesis of Oxaspirobicyclic Butenolides via a Domino Michael Addition/Aldol Reaction/γ-Lactonization Sequence." ChemInform 41, № 39 (2 вересня 2010): no. http://dx.doi.org/10.1002/chin.201039162.
Повний текст джерелаAl Majid, Abdullah M. A., Mohammad Shahidul Islam, Assem Barakat, Mohamed H. M. Al-Agamy та Mu Naushad. "Facile and Promising Method for Michael Addition of Indole and Pyrrole to Electron-Deficienttrans-β-Nitroolefins Catalyzed by a Hydrogen Bond Donor Catalyst Feist’s Acid and Preliminary Study of Antimicrobial Activity". Scientific World Journal 2014 (2014): 1–15. http://dx.doi.org/10.1155/2014/649197.
Повний текст джерелаFilippini, Marie-Héléne, та Jean Rodriguez. "Facile Tandem Michael Addition-Retro Dieckmann Reaction of Cyclic β-Ketoesters: One-Pot Preparation of Polyfunctionalized Acyclic Derivatives". Synthetic Communications 25, № 2 (січень 1995): 245–52. http://dx.doi.org/10.1080/00397919508010813.
Повний текст джерелаWang, Hai-Feng, Hua Xiao, Xiao-Wei Wang, and Gang Zhao. "Tandem intramolecular oxa-Michael addition/decarboxylation reaction catalyzed by bifunctional cinchona alkaloids: facile synthesis of chiral flavanone derivatives." Tetrahedron 67, no. 30 (July 2011): 5389–94. http://dx.doi.org/10.1016/j.tet.2011.05.088.
Повний текст джерелаHuang, Chao, Yanqing Yin, Jiahui Guo, Jiong Wang, Baomin Fan та Lijuan Yang. "A facile synthesis of β-amino carbonyl compounds through an aza-Michael addition reaction under solvent-free conditions". RSC Advances 4, № 20 (2014): 10188. http://dx.doi.org/10.1039/c3ra46789a.
Повний текст джерелаLv, Qiulan, Ke Wang, Dazhuang Xu, Meiying Liu, Qing Wan, Hongye Huang, Shangdong Liang, Xiaoyong Zhang, and Yen Wei. "Facile preparation and biological imaging of luminescent polymeric nanoprobes with aggregation-induced emission characteristics through Michael addition reaction." Colloids and Surfaces B: Biointerfaces 145 (September 2016): 795–801. http://dx.doi.org/10.1016/j.colsurfb.2016.05.028.
Повний текст джерелаChaudhari, Tohasib Yusub, Sandeep K. Ginotra, and Vibha Tandon. "Facile access to functionalized indenes and fused quinolines by regioselective 5-enolexo-dig Michael addition and cyclization reactions." Organic & Biomolecular Chemistry 15, no. 44 (2017): 9319–30. http://dx.doi.org/10.1039/c7ob02498c.
Повний текст джерелаSaha, Mithu, Jahar Dey, Kochi Ismail, and Amarta K. Pal. "Facile Microwave-Promoted Knoevenagel Condensation and the Combination of Knoevenagel/ Michael addition Reaction in Aqueous Medium Containing Ionic Surfactant." Letters in Organic Chemistry 8, no. 8 (October 1, 2011): 554–58. http://dx.doi.org/10.2174/157017811797249272.
Повний текст джерелаYaragorla, Srinivasarao, and G. Srikanth Kumar. "ChemInform Abstract: A Facile Method for the Synthesis of Various 3-Substituted Indoles via Michael Addition Reaction Using NbCl5." ChemInform 46, no. 45 (October 22, 2015): no. http://dx.doi.org/10.1002/chin.201545134.
Повний текст джерелаEid, Elshimaa M., Huwaida M. E. Hassaneen, Ismail A. Abdelhamid, and Ahmed H. M. Elwahy. "Facile one‐pot, three‐component synthesis of novel bis(heterocycles) incorporating thieno[2,3‐ b ]thiophenes via Michael addition reaction." Journal of Heterocyclic Chemistry 57, no. 5 (May 2020): 2243–55. http://dx.doi.org/10.1002/jhet.3945.
Повний текст джерелаZheng, Zhihao, Pang Xiao, Huimin Ruan, Junbin Liao, Congjie Gao, Bart Van der Bruggen, and Jiangnan Shen. "Mussel-Inspired Surface Functionalization of AEM for Simultaneously Improved Monovalent Anion Selectivity and Antibacterial Property." Membranes 9, no. 3 (March 6, 2019): 36. http://dx.doi.org/10.3390/membranes9030036.
Повний текст джерелаWang, Hai-Feng, Hua Xiao, Xiao-Wei Wang, and Gang Zhao. "ChemInform Abstract: Tandem Intramolecular Oxa-Michael Addition/Decarboxylation Reaction Catalyzed by Bifunctional Cinchona Alkaloids: Facile Synthesis of Chiral Flavanone Derivatives." ChemInform 42, no. 48 (November 3, 2011): no. http://dx.doi.org/10.1002/chin.201148143.
Повний текст джерелаHuang, Chao, Yanqing Yin, Jiahui Guo, Jiong Wang, Baomin Fan та Lijuan Yang. "ChemInform Abstract: A Facile Synthesis of β-Amino Carbonyl Compounds Through an Aza-Michael Addition Reaction under Solvent-Free Conditions." ChemInform 45, № 40 (18 вересня 2014): no. http://dx.doi.org/10.1002/chin.201440038.
Повний текст джерелаFILIPPINI, M. H., and J. RODRIGUEZ. "ChemInform Abstract: Facile Tandem Michael Addition-Retro Dieckmann Reaction of Cyclic . beta.-Ketoesters: One-Pot Preparation of Polyfunctionalized Acyclic Derivatives." ChemInform 26, no. 25 (August 17, 2010): no. http://dx.doi.org/10.1002/chin.199525088.
Повний текст джерелаXiong, Kaiqin, Pengkai Qi, Ying Yang, Xiangyang Li, Hua Qiu, Xin Li, Ru Shen, Qiufen Tu, Zhilu Yang, and Nan Huang. "Facile immobilization of vascular endothelial growth factor on a tannic acid-functionalized plasma-polymerized allylamine coating rich in quinone groups." RSC Advances 6, no. 21 (2016): 17188–95. http://dx.doi.org/10.1039/c5ra25917g.
Повний текст джерелаNayab, Sana, Vanessa Trouillet, Hartmut Gliemann, Peter G. Weidler, Iqra Azeem, Saadia R. Tariq, Anja S. Goldmann, Christopher Barner-Kowollik, and Basit Yameen. "Reversible Diels–Alder and Michael Addition Reactions Enable the Facile Postsynthetic Modification of Metal–Organic Frameworks." Inorganic Chemistry 60, no. 7 (March 17, 2021): 4397–409. http://dx.doi.org/10.1021/acs.inorgchem.0c02492.
Повний текст джерелаPesyan, Nader Noroozi, Narmin Akhteh, Hana Batmani, Barış Anıl, and Ertan Şahin. "A Facile and Catalyst-free Synthesis of Hexahydroacridine-1,8(2H,5H )-dione and Octahydroacridin-10(1H )-yl)thiourea Derivatives: Inter- and Intramolecular Aza-Michael addition." Heterocyclic Communications 26, no. 1 (March 10, 2020): 26–32. http://dx.doi.org/10.1515/hc-2020-0005.
Повний текст джерела