Статті в журналах з теми "Michael Carlow"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Michael Carlow".
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.
Morrissey, Thomas J. "A Man of the Universal Church: Peter James Kenney, S.J., 1779–1841." Recusant History 24, no. 3 (May 1999): 320–34. http://dx.doi.org/10.1017/s0034193200002545.
Повний текст джерелаYanai, Hikaru, Osamu Kobayashi, Kenji Takada, Takuya Isono, Toshifumi Satoh, and Takashi Matsumoto. "Sequential Mukaiyama–Michael reaction induced by carbon acids." Chemical Communications 52, no. 16 (2016): 3280–83. http://dx.doi.org/10.1039/c5cc10115h.
Повний текст джерелаBosica, Giovanna, and Kurt Polidano. "Solvent-Free Henry and Michael Reactions with Nitroalkanes Promoted by Potassium Carbonate as a Versatile Heterogeneous Catalyst." Journal of Chemistry 2017 (2017): 1–9. http://dx.doi.org/10.1155/2017/6267036.
Повний текст джерелаHarwood, Buie, and Allan Hing. "Michael Graves' Carlos Hall Reviewed." Journal of Interior Design 13, no. 1 (May 1987): 37–44. http://dx.doi.org/10.1111/j.1939-1668.1987.tb00104.x.
Повний текст джерелаSilveira, Claudinei Taborda da, Carlos Henrique Sopchaki, Ricardo Michael Pinheiro Silveira, and Gisele Neuman. "Pré-Textuais." Raega - O Espaço Geográfico em Análise 31 (August 25, 2014): 1. http://dx.doi.org/10.5380/raega.v31i0.37605.
Повний текст джерелаSilveira, Claudinei Taborda da, Carlos Henrique Sopchaki, Ricardo Michael Pinheiro Silveira, and Gisele Neuman. "Nota Editorial." Raega - O Espaço Geográfico em Análise 31 (August 25, 2014): 6. http://dx.doi.org/10.5380/raega.v31i0.37606.
Повний текст джерелаRudorf, Wolf-Dieter, and Ralf Schwarz. "Intramolecular Michael and Anti-Michael Additions to Carbon-Carbon Triple Bonds." Synlett 1993, no. 06 (1993): 369–74. http://dx.doi.org/10.1055/s-1993-22461.
Повний текст джерелаShim, Jae Ho, Byung Kook Ahn, Ji Yeon Lee, Hyeon Soo Kim та Deok-Chan Ha. "Organocatalysis for the Asymmetric Michael Addition of Cycloketones and α, β-Unsaturated Nitroalkenes". Catalysts 11, № 8 (20 серпня 2021): 1004. http://dx.doi.org/10.3390/catal11081004.
Повний текст джерелаBallini, R., L. Barboni, G. Bosica, D. Fiorini, and A. Palmieri. "Synthesis of fine chemicals by the conjugate addition of nitroalkanes to electrophilic alkenes." Pure and Applied Chemistry 78, no. 10 (January 1, 2006): 1857–66. http://dx.doi.org/10.1351/pac200678101857.
Повний текст джерелаLee, P. T., D. Lowinsohn, and R. G. Compton. "The selective electrochemical detection of homocysteine in the presence of glutathione, cysteine, and ascorbic acid using carbon electrodes." Analyst 139, no. 15 (2014): 3755–62. http://dx.doi.org/10.1039/c4an00372a.
Повний текст джерелаRUDORF, W. D., and R. SCHWARZ. "ChemInform Abstract: Intramolecular Michael and Anti-Michael Additions to Carbon-Carbon Triple Bonds." ChemInform 25, no. 4 (August 19, 2010): no. http://dx.doi.org/10.1002/chin.199404293.
Повний текст джерелаMartínez, Jose I., Uxue Uria, Maria Muñiz, Efraím Reyes, Luisa Carrillo та Jose L. Vicario. "Organocatalytic and enantioselective Michael reaction between α-nitroesters and nitroalkenes. Syn/anti-selectivity control using catalysts with the same absolute backbone chirality". Beilstein Journal of Organic Chemistry 11 (14 грудня 2015): 2577–83. http://dx.doi.org/10.3762/bjoc.11.277.
Повний текст джерелаShim, Jae Ho, Seok Hyun Cheun, Hyeon Soo Kim та Deok-Chan Ha. "Organocatalysis for the Asymmetric Michael Addition of Aldehydes and α,β-Unsaturated Nitroalkenes". Catalysts 12, № 2 (20 січня 2022): 121. http://dx.doi.org/10.3390/catal12020121.
Повний текст джерелаDarvesh, Sultan, Andrew S. Grant, David I. MaGee, and Zdenek Valenta. "Synthetic studies towards bruceantin. Part 1. Establishment of the carbon network." Canadian Journal of Chemistry 69, no. 4 (April 1, 1991): 712–22. http://dx.doi.org/10.1139/v91-902.
Повний текст джерелаLiu, Wenzhu, Jiafu Xiao, Qiong Xu, Xianxiang Liu, Sheng Zhong, Hua Huang, Min Zheng, Steven Robert Kirk, and Dulin Yin. "Imidazolyl activated carbon refluxed with ethanediamine as reusable heterogeneous catalysts for Michael addition." RSC Advances 9, no. 1 (2019): 185–91. http://dx.doi.org/10.1039/c8ra09457h.
Повний текст джерелаShaikh, Melad, Kiran Kumar Atyam, Mahendra Sahu, and Kalluri V. S. Ranganath. "Enhanced reactivity and selectivity of asymmetric oxa-Michael addition of 2′-hydroxychalcones in carbon confined spaces." Chemical Communications 53, no. 44 (2017): 6029–32. http://dx.doi.org/10.1039/c7cc01096f.
Повний текст джерелаSánchez-Roselló, María, Carlos del Pozo, and Javier Miró. "Cross-Metathesis/Intramolecular (Hetero-)Michael Addition: A Convenient Sequence for the Generation of Carbo- and Heterocycles." Synthesis 49, no. 13 (May 4, 2017): 2787–802. http://dx.doi.org/10.1055/s-0036-1589497.
Повний текст джерелаD'Souza, Ozma J., Ronald J. Mascarenhas, Ashis K. Satpati, Irishi N. N. Namboothiri, Simon Detriche, Zineb Mekhalif, and Joseph Delhalle. "A multi-walled carbon nanotube/poly-2,6-dichlorophenolindophenol film modified carbon paste electrode for the amperometric determination ofl-tyrosine." RSC Advances 5, no. 111 (2015): 91472–81. http://dx.doi.org/10.1039/c5ra18329d.
Повний текст джерелаWani, Aabid A., Sumit S. Chourasiya, Deepika Kathuria, and Prasad V. Bharatam. "1,1-Diaminoazines as organocatalysts in phospha-Michael addition reactions." Chemical Communications 57, no. 88 (2021): 11717–20. http://dx.doi.org/10.1039/d1cc04657h.
Повний текст джерелаButtes, Stephen. "The Failure of Consuelo’s Designs: Carlos Fuentes and Trompe l’Oeil Modernity." Revista Canadiense de Estudios Hispánicos 41, no. 2 (January 10, 2017): 297–324. http://dx.doi.org/10.18192/rceh.v41i2.2148.
Повний текст джерелаLewandowska, Elzbieta, Stefan Kinastowski, and Stanislaw F. Wnuk. "Studies on the rearrangement of ortho-nitrobenzylidenemalonates and their Analogues to 2-aminobenzoate derivatives." Canadian Journal of Chemistry 80, no. 2 (February 1, 2002): 192–99. http://dx.doi.org/10.1139/v02-010.
Повний текст джерелаKlimek, Mark, and Keith Pearce. "The cost of computing." Physics World 35, no. 7 (August 1, 2022): 24iii—25i. http://dx.doi.org/10.1088/2058-7058/35/07/23.
Повний текст джерелаYu, Xuan, Hui Bai, Dong Wang, Zhaohai Qin, Jia-Qi Li, and Bin Fu. "A convenient approach to difluoromethylated all-carbon quaternary centers via Ni(ii)-catalyzed enantioselective Michael addition." RSC Advances 8, no. 35 (2018): 19402–8. http://dx.doi.org/10.1039/c8ra02853b.
Повний текст джерелаLei, Chuan-Wen, Chuan-Bao Zhang, Zhen-Hua Wang, Ke-Xin Xie, Jian-Qiang Zhao, Ming-Qiang Zhou, Xiao-Mei Zhang, Xiao-Ying Xu, and Wei-Cheng Yuan. "Coumarin-3-formylpyrazoles as 3-carbon synthons in cyclocondensation for the synthesis of spiro-fused pentacyclic spirooxindoles." Organic & Biomolecular Chemistry 18, no. 5 (2020): 845–50. http://dx.doi.org/10.1039/c9ob02434d.
Повний текст джерелаXie, Yili, Qiang Huang, Meiying Liu, Ke Wang, Qing Wan, Fengjie Deng, Long Lu, Xiaoyong Zhang, and Yen Wei. "Mussel inspired functionalization of carbon nanotubes for heavy metal ion removal." RSC Advances 5, no. 84 (2015): 68430–38. http://dx.doi.org/10.1039/c5ra08908e.
Повний текст джерелаZheng, Weiping, Jiayong Zhang, Shuang Liu, Chengbin Yu, and Zhiwei Miao. "Asymmetric synthesis of spiro[chroman-3,3′-pyrazol] scaffolds with an all-carbon quaternary stereocenter via a oxa-Michael–Michael cascade strategy with bifunctional amine-thiourea organocatalysts." RSC Advances 5, no. 111 (2015): 91108–13. http://dx.doi.org/10.1039/c5ra17792h.
Повний текст джерелаCheng, Wen-Fu, Ling-Yan Chen, Fang-Fang Xu, Wei-Yu Lin, Xinfeng Ren, and Ya Li. "Organocatalytic asymmetric Michael addition between 3-subsituted oxindoles and enals catalyzed by camphor sulfonyl hydrazine." Organic & Biomolecular Chemistry 17, no. 4 (2019): 885–91. http://dx.doi.org/10.1039/c8ob02934b.
Повний текст джерелаDong, Xiao-Yan, та Da-Ming Du. "Asymmetric 1,4-Michael Addition Reaction of Azadienes with α-Thiocyanoindanones Catalyzed by Bifunctional Chiral Squaramide". Molecules 26, № 17 (25 серпня 2021): 5146. http://dx.doi.org/10.3390/molecules26175146.
Повний текст джерелаBoyko, Yaroslav Dmitrievich, Valentin Sergeevich Dorokhov, Alexey Yu Sukhorukov, and Sema Leibovich Ioffe. "Conjugated nitrosoalkenes as Michael acceptors in carbon–carbon bond forming reactions: a review and perspective." Beilstein Journal of Organic Chemistry 13 (October 23, 2017): 2214–34. http://dx.doi.org/10.3762/bjoc.13.220.
Повний текст джерелаYang, Wei, Yu Zhou, Haifeng Sun, Lei Zhang, Fei Zhao, and Hong Liu. "One-pot metal-free synthesis of highly substituted pyrroles from 2-acetyl-3-methylene-1,4-dicarbonyl compounds and primary amines via TBHP and activated carbon oxidative aromatization of dihydropyrrole." RSC Adv. 4, no. 29 (2014): 15007–10. http://dx.doi.org/10.1039/c3ra47782g.
Повний текст джерелаVazquez, Carlos Adrian. "Reflections from Inside." Boom 6, no. 2 (2016): 60–73. http://dx.doi.org/10.1525/boom.2016.6.2.60.
Повний текст джерелаMontenegro-Sustaita, Mabel M., Hugo A. Jiménez-Vázquez, Elena Vargas-Díaz, J. Enrique Herbert-Pucheta, and L. Gerardo Zepeda-Vallejo. "Structural Analysis of the Michael-Michael Ring Closure (MIMIRC) Reaction Products." Molecules 27, no. 9 (April 28, 2022): 2810. http://dx.doi.org/10.3390/molecules27092810.
Повний текст джерелаAllen, Michael. "The huge carbon footprint of large-scale computing." Physics World 35, no. 3 (August 1, 2022): 46–50. http://dx.doi.org/10.1088/2058-7058/35/03/32.
Повний текст джерелаBraga, Ruy Gomes, and Deni Alfaro Rubbo. "Dois mestres na periferia do capitalismo Michael Löwy e Mariátegui." Caderno CRH 31, no. 83 (January 24, 2019): 321–34. http://dx.doi.org/10.9771/ccrh.v31i83.25022.
Повний текст джерелаNi, Jixiang, Àlex Cristòfol та Arjan W. Kleij. "Formation of β-cyano-ketones through cyanide-promoted ring-opening of cyclic organic carbonates". Organic Chemistry Frontiers 8, № 16 (2021): 4520–26. http://dx.doi.org/10.1039/d1qo00770j.
Повний текст джерелаKhatua, Arindam, Pranay Shyamal, Souvik Pal, Ayan Mondal, and Alakesh Bisai. "Concise total syntheses of bis(cyclotryptamine) alkaloids via thio-urea catalyzed one-pot sequential Michael addition." Chemical Communications 58, no. 24 (2022): 3929–32. http://dx.doi.org/10.1039/d2cc01008a.
Повний текст джерелаHao, Xin-Qi, Cong Wang, Shuang-Liang Liu, Xiao Wang, Li Wang, Jun-Fang Gong та Mao-Ping Song. "Cobalt(ii)/(imidazoline–oxazoline)-catalyzed enantioselective Michael addition of 2-acetyl azaarenes to β-CF3-β-disubstituted nitroalkenes". Organic Chemistry Frontiers 4, № 2 (2017): 308–12. http://dx.doi.org/10.1039/c6qo00562d.
Повний текст джерелаZhu, Xiao-Yu, Mei-Heng Lv, Ya-Nan Zhao, Li-Yan Lan, Wen-Ze Li, and Lin-Jiu Xiao. "Organocatalytic sulfa-Michael/aldol cascade: constructing functionalized 2,5-dihydrothiophenes bearing a quaternary carbon stereocenter." RSC Advances 8, no. 59 (2018): 34000–34003. http://dx.doi.org/10.1039/c8ra04325f.
Повний текст джерелаSu, Shikuan, Jianxiong Li, Mingming Sun, Hongbin Zhao, Yali Chen, and Jian Li. "A domino reaction of 2-isocyanophenyloxyacrylate and aryne to synthesize arenes with vicinal olefin and benzoxazole." Chemical Communications 54, no. 69 (2018): 9611–14. http://dx.doi.org/10.1039/c8cc05735d.
Повний текст джерелаMohapatra, Seetaram, Nilofar Baral, Nilima Priyadarsini Mishra, Pravati Panda та Sabita Nayak. "Michael Addition of Imidazole to α, β -Unsaturated Carbonyl/Cyano Compound". Open Chemistry Journal 5, № 1 (30 квітня 2018): 18–31. http://dx.doi.org/10.2174/1874842201805010018.
Повний текст джерелаBanerjee, Subhash. "The remarkable catalytic activity of ultra-small free-CeO2 nanoparticles in selective carbon–carbon bond formation reactions in water at room temperature." New Journal of Chemistry 39, no. 7 (2015): 5350–53. http://dx.doi.org/10.1039/c5nj00500k.
Повний текст джерелаStrohmeier, Gernot A., Tanja Sović, Georg Steinkellner, Franz S. Hartner, Aleksandra Andryushkova, Thomas Purkarthofer, Anton Glieder, Karl Gruber, and Herfried Griengl. "Investigation of lipase-catalyzed Michael-type carbon–carbon bond formations." Tetrahedron 65, no. 29-30 (July 2009): 5663–68. http://dx.doi.org/10.1016/j.tet.2009.05.042.
Повний текст джерелаLavine, Michael. "A note on bounding monte carlo variances michael lavine." Communications in Statistics - Theory and Methods 21, no. 10 (January 1992): 2855–60. http://dx.doi.org/10.1080/03610929208830948.
Повний текст джерелаBerdet, Marc. "Entrevista a Michael Löwy, galardonado con el Premio europeo Walter Benjamin 2020." Acta Poética 42, no. 2 (June 22, 2021): 171–85. http://dx.doi.org/10.19130/iifl.ap.2021.2.18128.
Повний текст джерелаLiu, Hsing-Jang, та Hla Wynn. "Cyanothiolacetate as a masked β-hydroxyproprionitrile carbanion in Michael reactions". Canadian Journal of Chemistry 64, № 4 (1 квітня 1986): 649–57. http://dx.doi.org/10.1139/v86-105.
Повний текст джерелаNájera, Carmen, José Miguel Sansano, and Enrique Gómez-Bengoa. "Heterocycle-based bifunctional organocatalysts in asymmetric synthesis." Pure and Applied Chemistry 88, no. 6 (June 1, 2016): 561–78. http://dx.doi.org/10.1515/pac-2016-0403.
Повний текст джерелаDe Novion, Jacques, Rebecca Lemos Igreja, and Camilo Negri. "O PAPEL DAS ESQUERDAS NO MUNDO." Abya-yala: Revista sobre Acesso à Justiça e Direitos nas Américas 2, no. 3 (December 30, 2018): 246–60. http://dx.doi.org/10.26512/abyayala.v2i3.23330.
Повний текст джерелаMeng, Fan-Tao, Jing-Long Chen, Xiao-Yan Qin, Tian-Shu Zhang, Shu-Jiang Tu, Bo Jiang, and Wen-Juan Hao. "Gold self-relay catalysis for accessing functionalized cyclopentenones bearing an all-carbon quaternary stereocenter." Organic Chemistry Frontiers 9, no. 1 (2022): 140–46. http://dx.doi.org/10.1039/d1qo01313k.
Повний текст джерелаGao, Lingzhi, Bin Cheng, Huijie Yue, Suyan Cao, Jiang-Li Wang, and Liang Xu. "A bioinspired approach for construction of the [7-5-6-5] all-carbon tetracyclic core of logeracemin A." Organic Chemistry Frontiers 6, no. 6 (2019): 813–16. http://dx.doi.org/10.1039/c9qo00062c.
Повний текст джерелаHuang, You-ming, Chang-wu Zheng, and Gang Zhao. "Organocatalyzed aza-Michael–Michael cascade reactions to construct spirooxindole tetrahydroquinolines with all-carbon chiral centers." RSC Advances 3, no. 38 (2013): 16999. http://dx.doi.org/10.1039/c3ra42783h.
Повний текст джерела