최소 단어 이상 선택하여야 합니다.
최대 10 단어까지만 선택 가능합니다.
다음과 같은 기능을 한번의 로그인으로 사용 할 수 있습니다.
NTIS 바로가기Organic process research & development, v.25 no.5, 2021년, pp.1176 - 1183
Jeon, Hyun Ji (Center for Catalytic Hydrocarbon Functionalizations , Institute for Basic Science (IBS) , Daejeon 34141 , South Korea) , Lee, Wongyu (Center for Catalytic Hydrocarbon Functionalizations , Institute for Basic Science (IBS) , Daejeon 34141 , South Korea) , Seo, Sangwon , Chang, Sukbok
Herein, we describe the scalability and sustainability investigations toward the visible light-mediated amidation of aldehydes with N-chloro-N-sodio-carbamates. The practicality credentials of N-chloro-N-sodio-carbamates for their use in multigram scale amidation reactions are proven by scale-up pro...
Asadi, A., Patrick, B. O., Perrin, D. M.. Janus-AT Bases: Synthesis, Self-Assembly, and Solid State Structures. Journal of organic chemistry, vol.72, no.2, 466-475.
Leung, Leo M. H., Gibson, Vicky, Linclau, Bruno. A Linchpin Carbacyclization Approach for the Synthesis of Carbanucleosides. Journal of organic chemistry, vol.73, no.23, 9197-9206.
Sheshenev, Andrey E., Boltukhina, Ekaterina V., Hii, King Kuok (Mimi). Levonantradol: asymmetric synthesis and structural analysis. Chemical communications : Chem comm, vol.49, no.35, 3685-3687.
Largy, Eric, Liu, Wenbo, Hasan, Abid, Perrin, David M.. Base‐Pairing Behavior of a Carbocyclic Janus‐AT Nucleoside Analogue Capable of Recognizing A and T within a DNA Duplex. Chembiochem : a European journal of chemical biology, vol.14, no.16, 2199-2208.
Cankař, Petr, Popa, Igor, Trávníček, Zdeněk, Stýskala, Jakub, Hradil, Pavel, Slouka, Jan. Synthesis of 1‐Aminocodeine as a Synthon for Other Codeine Derivatives. European journal of organic chemistry, vol.2013, no.27, 6062-6068.
Vivier, Delphine, Soussia, Ismail Ben, Rodrigues, Nuno, Lolignier, Stéphane, Devilliers, Maïly, Chatelain, Franck C., Prival, Laetitia, Chapuy, Eric, Bourdier, Geoffrey, Bennis, Khalil, Lesage, Florian, Eschalier, Alain, Busserolles, Jérôme, Ducki, Sylvie. Development of the First Two-Pore Domain Potassium Channel TWIK-Related K+ Channel 1-Selective Agonist Possessing in Vivo Antinociceptive Activity. Journal of medicinal chemistry, vol.60, no.3, 1076-1088.
Liu, Ju, Gong, Yilin, Shi, Jiantao, Hao, Xuechen, Wang, Yang, Zhou, Yunpeng, Hou, Yunlei, Liu, Yajing, Ding, Shi, Chen, Ye. Design, synthesis and biological evaluation of novel N-[4-(2-fluorophenoxy)pyridin-2-yl]cyclopropanecarboxamide derivatives as potential c-Met kinase inhibitors. European journal of medicinal chemistry, vol.194, 112244-.
Dander, Jacob E., Garg, Neil K.. Breaking Amides using Nickel Catalysis. ACS catalysis, vol.7, no.2, 1413-1423.
Boit, Timothy B., Bulger, Ana S., Dander, Jacob E., Garg, Neil K.. Activation of C-O and C-N Bonds Using Non-Precious-Metal Catalysis. ACS catalysis, vol.10, 12109-12126.
Valeur, Eric, Bradley, Mark. Amide bond formation: beyond the myth of coupling reagents. Chemical Society reviews, vol.38, no.2, 606-631.
Pattabiraman, Vijaya R., Bode, Jeffrey W.. Rethinking amide bond synthesis. Nature, vol.480, no.7378, 471-479.
Chen, Cheng, Verpoort, Francis, Wu, Qiongyou. Atom-economic dehydrogenative amide synthesis via ruthenium catalysis. RSC advances, vol.6, no.60, 55599-55607.
de Figueiredo, Renata Marcia, Suppo, Jean-Simon, Campagne, Jean-Marc. Nonclassical Routes for Amide Bond Formation. Chemical reviews, vol.116, no.19, 12029-12122.
Narendar Reddy, Thatikonda, Beatriz, Adilson, Jayathirtha Rao, Vaidya, de Lima, Dênis Pires. Carbonyl Compounds′ Journey to Amide Bond Formation. Chemistry, an Asian journal, vol.14, no.3, 344-388.
Seiller, Bénédicte, Heins, Dorothee, Bruneau, Christian, H. Dixneuf, Pierre. Efficient preparations of acylamides, acylcarbamates and acylureas from alk-1-en-2-yl esters. Tetrahedron, vol.51, no.40, 10901-10912.
Thulam, Vijaya Kumar, Kotte, Subhash Chandra Bose, Sanjay Kumar, H., Murali, P.M., Mukkanti, K., Mainker, Prathama S.. A novel and efficient method for N-acylation of sulfonamides and carbamates: Their biological evaluation towards anti Malassezia activity. Journal of pharmacy research, vol.7, no.2, 195-199.
Papadopoulos, E. P.. Reactions of pyrrole with isocyanates. Preparation and reactions of N-ethoxy-carbonylpyrrole-2-carboxamide and pyrrole-1,2-dicarboximide. Journal of organic chemistry, vol.37, no.3, 351-355.
Lenz, George R., Woo, Chi Min, Hawkins, Bruce L.. Reaction of isoquinoline enamides with electrophiles. Journal of organic chemistry, vol.47, no.16, 3049-3053.
Komuro, Katsuhiro, Nagaki, Aiichiro, Shimoda, Hiroki, Uwamori, Masahiro, Yoshida, Jun-ichi, Nakada, Masahisa. Efficient Preparation of Cyclic α-Alkylidene β-Oxo Imides by Using a Flow Microreactor System. Synlett : accounts and rapid communications in synthetic organic chemistry, vol.29, no.15, 1989-1994.
Dondoni, Alessandro, Marra, Alberto, Massi, Alessandro. Hybrid Solution/Solid-Phase Synthesis of Oligosaccharides by Using Trichloroacetyl Isocyanate as Sequestration-Enabling Reagent of Sugar Alcohols. Angewandte Chemie. international edition, vol.44, no.11, 1672-1676.
Chen, Jia-Rong, Hu, Xiao-Qiang, Lu, Liang-Qiu, Xiao, Wen-Jing. Visible light photoredox-controlled reactions of N-radicals and radical ions. Chemical Society reviews, vol.45, no.8, 2044-2056.
Xiong, Tao, Zhang, Qian. New amination strategies based on nitrogen-centered radical chemistry. Chemical Society reviews, vol.45, no.11, 3069-3087.
Kärkäs, Markus D.. Photochemical Generation of Nitrogen-Centered Amidyl, Hydrazonyl, and Imidyl Radicals: Methodology Developments and Catalytic Applications. ACS catalysis, vol.7, no.8, 4999-5022.
Capaldo, Luca, Ravelli, Davide. Hydrogen Atom Transfer (HAT): A Versatile Strategy for Substrate Activation in Photocatalyzed Organic Synthesis. European journal of organic chemistry, vol.2017, no.15, 2056-2071.
Chang, Joyce Wei Wei, Chan, Philip Wai Hong. Highly Efficient Ruthenium(II) Porphyrin Catalyzed Amidation of Aldehydes. Angewandte Chemie. international edition, vol.47, no.6, 1138-1140.
Li, Junmei, Xu, Fan, Zhang, Yong, Shen, Qi. Heterobimetallic Lanthanide/Sodium Phenoxides: Efficient Catalysts for Amidation of Aldehydes with Amines. Journal of organic chemistry, vol.74, no.6, 2575-2577.
Ghosh, Subhash Chandra, Ngiam, Joyce S. Y., Seayad, Abdul M., Tuan, Dang Thanh, Chai, Christina L. L., Chen, Anqi. Copper-Catalyzed Oxidative Amidation of Aldehydes with Amine Salts: Synthesis of Primary, Secondary, and Tertiary Amides. Journal of organic chemistry, vol.77, no.18, 8007-8015.
Jin, Li-Mei, Lu, Hongjian, Cui, Yuan, Lizardi, Christopher L., Arzua, Thiago N., Wojtas, Lukasz, Cui, Xin, Zhang, X. Peter. Selective radical amination of aldehydic C(sp2)-H bonds with fluoroaryl azides via Co(II)-based metalloradical catalysis: synthesis of N-fluoroaryl amides from aldehydes under neutral and nonoxidative conditions. Chemical science, vol.5, no.6, 2422-2427.
Whittaker, Aaron M., Dong, Vy M.. Nickel‐Catalyzed Dehydrogenative Cross‐Coupling: Direct Transformation of Aldehydes into Esters and Amides. Angewandte Chemie. international edition, vol.54, no.4, 1312-1315.
Nguyen, Trang T., Hull, Kami L.. Rhodium-Catalyzed Oxidative Amidation of Sterically Hindered Aldehydes and Alcohols. ACS catalysis, vol.6, no.12, 8214-8218.
Leow, Dasheng. Phenazinium Salt-Catalyzed Aerobic Oxidative Amidation of Aromatic Aldehydes. Organic letters, vol.16, no.21, 5812-5815.
Iqbal, Naeem, Cho, Eun Jin. Visible-Light-Mediated Synthesis of Amides from Aldehydes and Amines via in Situ Acid Chloride Formation. Journal of organic chemistry, vol.81, no.5, 1905-1911.
Papadopoulos, Giorgos N., Kokotos, Christoforos G.. One-Pot Amide Bond Formation from Aldehydes and Amines via a Photoorganocatalytic Activation of Aldehydes. Journal of organic chemistry, vol.81, no.16, 7023-7028.
Pandey, Ganesh, Koley, Suvajit, Talukdar, Ranadeep, Sahani, Pramod Kumar. Cross-Dehydrogenating Coupling of Aldehydes with Amines/R-OTBS Ethers by Visible-Light Photoredox Catalysis: Synthesis of Amides, Esters, and Ureas. Organic letters, vol.20, no.18, 5861-5865.
Constable, David J. C., Dunn, Peter J., Hayler, John D., Humphrey, Guy R., Leazer, Jr., Johnnie L., Linderman, Russell J., Lorenz, Kurt, Manley, Julie, Pearlman, Bruce A., Wells, Andrew, Zaks, Aleksey, Zhang, Tony Y.. Key green chemistry research areas—a perspective from pharmaceutical manufacturers. Green chemistry : an international journal and green chemistry resource : GC, vol.9, no.5, 411-420.
Bryan, Marian C., DunnRetired., Peter J., Entwistle, David, Gallou, Fabrice, Koenig, Stefan G., Hayler, John D., Hickey, Matthew R., Hughes, Shaun, Kopach, Michael E., Moine, Gerard, Richardson, Paul, Roschangar, Frank, Steven, Alan, Weiberth, Franz J.. Key Green Chemistry research areas from a pharmaceutical manufacturers’ perspective revisited. Green chemistry : an international journal and green chemistry resource : GC, vol.20, no.22, 5082-5103.
Braun, Marie-Gabrielle, Engl, Oliver, Fraunhoffer, Kenneth, Hayler, John, Hickey, Matthew, Latham, Jonathan, Lovelle, Lucie E., McLaws, Mark, Richardson, Paul, Roosen, Philipp C., Steven, Alan, Terrett, Jack A., White, Timothy, Yin, Jingjun. Green Chemistry Articles of Interest to the Pharmaceutical Industry. Organic process research & development, vol.24, no.6, 897-908.
Federsel, Hans-Jürgen. Chemical Process Research and Development in the 21st Century: Challenges, Strategies, and Solutions from a Pharmaceutical Industry Perspective. Accounts of chemical research, vol.42, no.5, 671-680.
Gwon, Donghyeon, Hwang, Heejun, Kim, Hye Kyung, Marder, Seth R., Chang, Sukbok. Synthesis of 8‐Aminoquinolines by Using Carbamate Reagents: Facile Installation and Deprotection of Practical Amidating Groups. Chemistry : a European journal, vol.21, no.48, 17200-17204.
Xie, Weilong, Yoon, Jung Hee, Chang, Sukbok. (NHC)Cu-Catalyzed Mild C–H Amidation of (Hetero)arenes with Deprotectable Carbamates: Scope and Mechanistic Studies. Journal of the American Chemical Society, vol.138, no.38, 12605-12614.
Herranz, Eugenio, Sharpless, K. Barry. Osmium-catalyzed vicinal oxyamination of olefins by N-chloro-N-metallocarbamates. Journal of organic chemistry, vol.45, no.13, 2710-2713.
Tilstam, U., Weinmann, H.. Trichloroisocyanuric Acid: A Safe and Efficient Oxidant. Organic process research & development, vol.6, no.4, 384-393.
Gaspa, Silvia, Carraro, Massimo, Pisano, Luisa, Porcheddu, Andrea, De Luca, Lidia. Trichloroisocyanuric Acid: a Versatile and Efficient Chlorinating and Oxidizing Reagent. European journal of organic chemistry, vol.2019, no.22, 3544-3552.
Capello, Christian, Fischer, Ulrich, Hungerbühler, Konrad. What is a green solvent? A comprehensive framework for the environmental assessment of solvents. Green chemistry : an international journal and green chemistry resource : GC, vol.9, no.9, 927-934.
Prat, Denis, Pardigon, Olivier, Flemming, Hans-Wolfram, Letestu, Sylvie, Ducandas, Véronique, Isnard, Pascal, Guntrum, Eberhard, Senac, Thomas, Ruisseau, Stéphane, Cruciani, Paul, Hosek, Patrik. Sanofi’s Solvent Selection Guide: A Step Toward More Sustainable Processes. Organic process research & development, vol.17, no.12, 1517-1525.
Henderson, Richard K., Jiménez-González, Concepción, Constable, David J. C., Alston, Sarah R., Inglis, Graham G. A., Fisher, Gail, Sherwood, James, Binks, Steve P., Curzons, Alan D.. Expanding GSK's solvent selection guide – embedding sustainability into solvent selection starting at medicinal chemistry. Green chemistry : an international journal and green chemistry resource : GC, vol.13, no.4, 854-862.
Diorazio, Louis J., Hose, David R. J., Adlington, Neil K.. Toward a More Holistic Framework for Solvent Selection. Organic process research & development, vol.20, no.4, 760-773.
Clarke, Coby J., Tu, Wei-Chien, Levers, Oliver, Bröhl, Andreas, Hallett, Jason P.. Green and Sustainable Solvents in Chemical Processes. Chemical reviews, vol.118, no.2, 747-800.
MacMillan, Donna S., Murray, Jane, Sneddon, Helen F., Jamieson, Craig, Watson, Allan J. B.. Evaluation of alternative solvents in common amide coupling reactions: replacement of dichloromethane and N,N-dimethylformamide. Green chemistry : an international journal and green chemistry resource : GC, vol.15, no.3, 596-600.
Sabatini, Marco T., Boulton, Lee. T., Sneddon, Helen F., Sheppard, Tom D.. A green chemistry perspective on catalytic amide bond formation. Nature catalysis, vol.2, no.1, 10-17.
Al Musaimi, Othman, de la Torre, Beatriz G., Albericio, Fernando. Greening Fmoc/tBu solid-phase peptide synthesis. Green chemistry : an international journal and green chemistry resource : GC, vol.22, no.4, 996-1018.
Le, Chi “Chip”, Wismer, Michael K., Shi, Zhi-Cai, Zhang, Rui, Conway, Donald V., Li, Guoqing, Vachal, Petr, Davies, Ian W., MacMillan, David W. C.. A General Small-Scale Reactor To Enable Standardization and Acceleration of Photocatalytic Reactions. ACS central science, vol.3, no.6, 647-653.
해당 논문의 주제분야에서 활용도가 높은 상위 5개 콘텐츠를 보여줍니다.
더보기 버튼을 클릭하시면 더 많은 관련자료를 살펴볼 수 있습니다.
*원문 PDF 파일 및 링크정보가 존재하지 않을 경우 KISTI DDS 시스템에서 제공하는 원문복사서비스를 사용할 수 있습니다.
※ AI-Helper는 부적절한 답변을 할 수 있습니다.