Journal articles on the topic 'Bromomalonate'
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Li, Qingrui, Yunnian Yin, Yabo Li, et al. "A simple approach to indeno-coumarins via visible-light-induced cyclization of aryl alkynoates with diethyl bromomalonate." Organic Chemistry Frontiers 6, no. 18 (2019): 3238–43. http://dx.doi.org/10.1039/c9qo00795d.
Full textKATO, EISHIN, MASAYUKI OYA, TADASHI ISO, and JUN-ISHI IWAO. "Conversion of thiols into disulfides with diethyl bromomalonate." CHEMICAL & PHARMACEUTICAL BULLETIN 34, no. 2 (1986): 486–95. http://dx.doi.org/10.1248/cpb.34.486.
Full textAmriev, R. A., L. V. Vinogradova, and F. K. Velichko. "Addition of diethyl bromomalonate and diethyl dibromomalonate to vinyltrimethylsilane." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 10 (1985): 2223–24. http://dx.doi.org/10.1007/bf00963269.
Full textTruksa, Scott V., Alan Nibler, Bruce S. Schatz, Kevin W. Krosley, and Gerald Jay Gleicher. "Benzylic hydrogen atom abstraction utilizing diethyl bromomalonate as a radical source." Journal of Organic Chemistry 57, no. 10 (1992): 2967–70. http://dx.doi.org/10.1021/jo00036a044.
Full textMenn, Jean-Christophe Le, André Tallec, and Jean Sarrazin. "Obtention de cyclopropanes gem-dicarboxylate par cyclocondensation de carbanions bromo- et chloromalonate sur des accepteurs de Michaël." Canadian Journal of Chemistry 69, no. 5 (1991): 761–67. http://dx.doi.org/10.1139/v91-113.
Full textBarton, William R., та Leo A. Paquette. "Generic synthesis of β-sultams via domino alkylation of bromomethanesulfonamides". Canadian Journal of Chemistry 82, № 2 (2004): 113–19. http://dx.doi.org/10.1139/v03-174.
Full textKang, Haixia, Jing Bai, Zhentao Xi, Manman Zhang, Yuqin Fu, and Dapeng Zou. "Reaction of 5(R)-(l-Menthoxy)-2(5H)-furanone with Diethyl Bromomalonate." Chinese Journal of Organic Chemistry 36, no. 8 (2016): 1915. http://dx.doi.org/10.6023/cjoc201601040.
Full textPapageorgiou, George, and John E. T. Corrie. "A strategy to avoid anomalousO-alkylation of 4-hydroxyindole by diethyl bromomalonate." Journal of Heterocyclic Chemistry 42, no. 6 (2005): 1101–4. http://dx.doi.org/10.1002/jhet.5570420610.
Full textGu, Guangmiao, Mengmeng Huang, Jung Keun Kim, Jianye Zhang, Yabo Li, and Yangjie Wu. "Visible-light-induced photocatalyst-free C-3 functionalization of indoles with diethyl bromomalonate." Green Chemistry 22, no. 8 (2020): 2543–48. http://dx.doi.org/10.1039/d0gc00292e.
Full textCoumbarides, Gregory Socrates, Marco Dingjan, Jason Eames, and Neluka Weerasooriya. "Investigations into the Bromination of Substituted Phenols using Diethyl Bromomalonate and Diethyl Dibromomalonate." Bulletin of the Chemical Society of Japan 74, no. 1 (2001): 179–80. http://dx.doi.org/10.1246/bcsj.74.179.
Full textBurshtein, K. Ya, G. V. Kryshtal', and L. A. Yanovskaya. "Factors affecting the direction of the reaction of bromomalonate ester with ?,?-unsaturated aldehydes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 6 (1985): 1303–4. http://dx.doi.org/10.1007/bf00956110.
Full textTRUKSA, S. V., A. NIBLER, B. S. SCHATZ, K. W. KROSLEY, and G. J. GLEICHER. "ChemInform Abstract: Benzylic Hydrogen Atom Abstraction Utilizing Diethyl Bromomalonate as a Radical Source." ChemInform 23, no. 42 (2010): no. http://dx.doi.org/10.1002/chin.199242104.
Full textMu, Siyu, Hongxia Li, Zhilin Wu, Junmei Peng, Jinyang Chen, and Weimin He. "Electrocatalytic Three-Component Synthesis of 4-Bromopyrazoles from Acetylacetone, Hydrazine and Diethyl Bromomalonate." Chinese Journal of Organic Chemistry 42, no. 12 (2022): 4292. http://dx.doi.org/10.6023/cjoc202211002.
Full textNemcsok, Tamás, Zsolt Rapi, Péter Bagi, Attila Oláh, György Keglevich, and Péter Bakó. "The Synthesis of Hydrobenzoin-Based Monoaza Crown Ethers and Their Application as Recyclable Enantioselective Catalysts." Catalysis Letters 150, no. 4 (2019): 930–38. http://dx.doi.org/10.1007/s10562-019-03013-0.
Full textNaveena Kumari, H. M., Manjunath Harihara Mathada, Mahesh Kumar, K. T. Suda, and K. M. Basavaraja. "Synthesis, Characterization, Antimicrobial Screening of 5-Bromobenzofuranyl Aryl Ureas and Carbamates." Asian Journal of Organic & Medicinal Chemistry 4, no. 4 (2019): 232–35. http://dx.doi.org/10.14233/ajomc.2019.ajomc-p215.
Full textCoumbarides, Gregory Socrates, Marco Dingjan, Jason Eames, and Neluka Weerasooriya. "ChemInform Abstract: Investigations into the Bromination of Substituted Phenols Using Diethyl Bromomalonate and Diethyl Dibromomalonate." ChemInform 32, no. 16 (2001): no. http://dx.doi.org/10.1002/chin.200116069.
Full textXuan, Yi-ning, Shao-zhen Nie, Li-ting Dong, Jun-min Zhang та Ming Yan. "Highly Enantioselective Synthesis of Nitrocyclopropanes via Organocatalytic Conjugate Addition of Bromomalonate to α,β-Unsaturated Nitroalkenes". Organic Letters 11, № 7 (2009): 1583–86. http://dx.doi.org/10.1021/ol900227j.
Full textSun, Jun-Chao, Jun-Lin Li, Cong-Bin Ji, Yi-Yuan Peng, and Xing-Ping Zeng. "Construction of Cyclopropa[c]coumarins via cascade Michael-alkylation process of 3-cyanocoumarin with 2-bromomalonate." Tetrahedron 76, no. 5 (2020): 130852. http://dx.doi.org/10.1016/j.tet.2019.130852.
Full textNédélec, J. Y., and K. Nohair. "Manganese(III)-Promoted Free-Radical Addition of Dimethyl Bromomalonate to Olefins Using an Electrochemical Regeneration Procedure." Synlett 1991, no. 09 (1991): 659–60. http://dx.doi.org/10.1055/s-1991-20832.
Full textLee, Hyun Joo, Sun Mi Kim, and Dae Young Kim. "Enantioselective synthesis of nitrocyclopropanes via conjugate addition of bromomalonate to nitroalkenes catalyzed by Ni(II) complexes." Tetrahedron Letters 53, no. 27 (2012): 3437–39. http://dx.doi.org/10.1016/j.tetlet.2012.04.072.
Full textChande, Madhukar S., та Udayashankar S. Bhat. "ChemInform Abstract: Synthesis of Novel Spiroglucosides and Fused Ring Heterocycles from Diethyl α-Acetamido-α-bromomalonate." ChemInform 31, № 9 (2010): no. http://dx.doi.org/10.1002/chin.200009054.
Full textOmran, Omran Abdellah. "The Reaction of Diethyl Bromomalonate with p-tert-Butylthia-calix[4]arene: An Approach to Asymmetrical Derivatives." Molecules 14, no. 5 (2009): 1755–61. http://dx.doi.org/10.3390/molecules14051755.
Full textKryshtal, Galina V., Galina M. Zhdankina, and Sergei G. Zlotin. "KOH-Promoted Synthesis of Oxirane Functional Derivatives from Diethyl Bromomalonate and Aldehydes under Phase-Transfer Catalysis Conditions." Mendeleev Communications 23, no. 1 (2013): 24–25. http://dx.doi.org/10.1016/j.mencom.2013.01.008.
Full textMartínez, Juan Pablo, Marc Garcia-Borràs, Sílvia Osuna, Jordi Poater, F. Matthias Bickelhaupt, and Miquel Solà. "Reaction Mechanism and Regioselectivity of the Bingel-Hirsch Addition of Dimethyl Bromomalonate to La@C 2v -C82." Chemistry - A European Journal 22, no. 17 (2016): 5953–62. http://dx.doi.org/10.1002/chem.201504668.
Full textH., A. H. EL-SHERIEF, MAHMOUD A.M., R. EL-EZBAWY S., and EL-WARETH A. O. SARHAN ABD. "Synthesis and Reactions of some New Benzimidazoles. Part-II." Journal of Indian Chemical Society Vol. 74, Jan 1997 (1997): 24–26. https://doi.org/10.5281/zenodo.5876923.
Full textHIROI, Kunio, and Yoshihisa ARINAGA. "Stereocontrolled Asymmetric Synthesis of Optically Active Acylcyclopropane Derivatives by Michael Additions of Bromomalonate to Chiral .ALPHA.-Acylvinylic Sulfoxides." CHEMICAL & PHARMACEUTICAL BULLETIN 42, no. 4 (1994): 985–87. http://dx.doi.org/10.1248/cpb.42.985.
Full textMiersch, Anne, Klaus Harms, and Gerhard Hilt. "Zinc-mediated addition of diethyl bromomalonate to alkynes for the cascade reaction towards polysubstituted pyranones and tetracarbonyl derivatives." Chem. Commun. 50, no. 5 (2014): 542–44. http://dx.doi.org/10.1039/c3cc46788k.
Full textLee, Hyun Joo, Sun Mi Kim, and Dae Young Kim. "ChemInform Abstract: Enantioselective Synthesis of Nitrocyclopropanes via Conjugate Addition of Bromomalonate to Nitroalkenes Catalyzed by Ni(II) Complexes." ChemInform 43, no. 41 (2012): no. http://dx.doi.org/10.1002/chin.201241053.
Full textNEDELEC, J. Y., and K. NOHAIR. "ChemInform Abstract: Manganese(III)-Promoted Free-Radical Addition of Dimethyl Bromomalonate to Olefins Using an Electrochemical Regeneration Procedure." ChemInform 23, no. 4 (2010): no. http://dx.doi.org/10.1002/chin.199204048.
Full textKANVINDE, M. N., R. M. KELKAR, and M. V. PARADKAR. "ChemInform Abstract: Unusual Behaviour of Diethyl Bromomalonate with 2-Hydroxydeoxybenzoins. Convenient Synthesis of 2-Aryl-3(2H)-benzofuranones." ChemInform 24, no. 35 (2010): no. http://dx.doi.org/10.1002/chin.199335175.
Full textKryshtal, Galina V., Galina M. Zhdankina, and Sergei G. Zlotin. "ChemInform Abstract: KOH-Promoted Synthesis of Oxirane Functional Derivatives from Diethyl Bromomalonate and Aldehydes under Phase-Transfer Catalysis Conditions." ChemInform 44, no. 21 (2013): no. http://dx.doi.org/10.1002/chin.201321098.
Full textBakandritsos, Aristides, Demetrios D. Chronopoulos, Petr Jakubec, et al. "High-Performance Supercapacitors Based on a Zwitterionic Network of Covalently Functionalized Graphene with Iron Tetraaminophthalocyanine." Advanced Functional Materials 28 (May 21, 2018): 1801111. https://doi.org/10.1002/adfm.201801111.
Full textPeng, Ru‐Fang, Guan‐Wu Wang, Ye‐Bing Shen, et al. "Solvent‐Free Reactions of Fullerenes with Diethyl Bromomalonate in the Presence of Inorganic Bases Under High‐Speed Vibration Milling Conditions." Synthetic Communications 34, no. 11 (2004): 2117–26. http://dx.doi.org/10.1081/scc-120030320.
Full textHaldar, Pranab, Bishnupada Dutta, Joyram Guin, and Jayanta K. Ray. "Uncatalyzed condensation between aryl-1,2-diamines and diethyl bromomalonate: a one-pot access to substituted ethyl 3-hydroxyquinoxaline-2-carboxylates." Tetrahedron Letters 48, no. 33 (2007): 5855–57. http://dx.doi.org/10.1016/j.tetlet.2007.06.065.
Full textHIROI, K., та Y. ARINAGA. "ChemInform Abstract: Stereocontrolled Asymmetric Synthesis of Optically Active Acylcyclopropane Derivatives by Michael Additions of Bromomalonate to Chiral α-Acylvinylic Sulfoxides." ChemInform 25, № 49 (2010): no. http://dx.doi.org/10.1002/chin.199449045.
Full textMiersch, Anne, Klaus Harms, and Gerhard Hilt. "ChemInform Abstract: Zinc-Mediated Addition of Diethyl Bromomalonate to Alkynes for the Cascade Reaction Towards Polysubstituted Pyranones and Tetracarbonyl Derivatives." ChemInform 45, no. 19 (2014): no. http://dx.doi.org/10.1002/chin.201419146.
Full textWolfe, Saul, Stephen Ro, Chan-Kyung Kim та Zheng Shi. "Synthesis and decarboxylation of Δ2-cephem-4,4-dicarboxylic acids". Canadian Journal of Chemistry 79, № 8 (2001): 1238–58. http://dx.doi.org/10.1139/v01-100.
Full textWei, Xian-Wen, Anthony G. Avent, Olga V. Boltalina та ін. "ChemInform Abstract: Reaction of C60F18 with Diethyl Bromomalonate: Diversion of the Bingel Reaction and Formation of the First 18π Annulenic Fullerene." ChemInform 33, № 16 (2010): no. http://dx.doi.org/10.1002/chin.200216121.
Full textDrandarov, Konstantin, Ioannis Tiritiris, and Willi Kantlehner. "Orthoamides and iminium salts, LXXXIX. Reactions of N,N,N′,N′,N″,N″,N′″,N′″-octamethyl-acetylene-bis(carboxamidinium) tetrafluoroborate with nucleophilic reagents – new methods for the preparation of amidinium salts and ketene aminalsa." Zeitschrift für Naturforschung B 70, no. 4 (2015): 225–41. http://dx.doi.org/10.1515/znb-2014-0204.
Full textOmran, Omran Abdellah. "Omran, O.-A. The Reaction of Diethyl Bromomalonate with p-tert-butylthiacalix[4]arene: An Approach to Asymmetrical Derivatives Molecules 2009, 14, 1755-1761." Molecules 14, no. 11 (2009): 4689. http://dx.doi.org/10.3390/molecules14114689.
Full textBesalú‐Sala, Pau, Josep M. Luis, and Miquel Solà. "Bingel–Hirsch Addition of Diethyl Bromomalonate to Ion‐Encapsulated Fullerenes M@C 60 (M=Ø, Li + , Na + , K + , Mg 2+ , Ca 2+ , and Cl − )." Chemistry – A European Journal 26, no. 63 (2020): 14481–87. http://dx.doi.org/10.1002/chem.202003208.
Full textLian, Xiao-Lei, Alafate Adili, Bin Liu, Zhong-Lin Tao, and Zhi-Yong Han. "Enantioselective [4 + 1] cycloaddition of ortho-quinone methides and bromomalonates under phase-transfer catalysis." Organic & Biomolecular Chemistry 15, no. 17 (2017): 3670–73. http://dx.doi.org/10.1039/c7ob00484b.
Full textYavari, Issa, Abbas Ali Esmaili, Sakineh Asghari, and Hamid Reza Bijanzadeh. "A New and Efficient One-pot Synthesis of Trialkyl 6-tert-Butylamino-2H-pyran-2-one-3,4,5-tricarboxylates." Journal of Chemical Research 23, no. 6 (1999): 368–69. http://dx.doi.org/10.1177/174751989902300612.
Full textHilt, Gerhard, Emre Babaoglu, and Klaus Harms. "Indium-Mediated Blaise-Type Reaction of Bromomalonates with Nitriles and Isocyanates." Synlett 27, no. 12 (2016): 1820–23. http://dx.doi.org/10.1055/s-0035-1561973.
Full textRouh, Hossein, Yao Tang, Ting Xu, et al. "Aggregation-Induced Synthesis (AIS): Asymmetric Synthesis via Chiral Aggregates." Research 2022 (August 12, 2022): 1–9. http://dx.doi.org/10.34133/2022/9865108.
Full textZhang, Yuheng, Lili Lin, Yushuang Chen, Xiaohua Liu, and Xiaoming Feng. "N ,N′ -Dioxide-Lanthanum(III)-Catalyzed Asymmetric Cyclopropanation of 2-Cyano-3-arylacrylates with 2-Bromomalonates." Advanced Synthesis & Catalysis 359, no. 11 (2017): 1831–36. http://dx.doi.org/10.1002/adsc.201700212.
Full textWu, Xingxing, Lei Li, and Junliang Zhang. "Direct Aza-Darzens Aziridination ofN-Tosylimines with 2-Bromomalonates for the Synthesis of Highly Functionalized Donor-Acceptor Aziridines." Advanced Synthesis & Catalysis 354, no. 18 (2012): 3485–89. http://dx.doi.org/10.1002/adsc.201200628.
Full textWu, Xingxing, Lei Li, and Junliang Zhang. "ChemInform Abstract: Direct Aza-Darzens Aziridination of N-Tosylimines with 2-Bromomalonates for the Synthesis of Highly Functionalized Donor-Acceptor Aziridines." ChemInform 44, no. 21 (2013): no. http://dx.doi.org/10.1002/chin.201321100.
Full textKim, Doyoung, Min Woo Ha, Suckchang Hong та ін. "Enantioselective Synthesis of Chiral α-Azido and α-Aryloxy Quaternary Stereogenic Centers via the Phase-Transfer-Catalyzed α-Alkylation of α-Bromomalonates, Followed by SN2 Substitution". Journal of Organic Chemistry 82, № 9 (2017): 4936–43. http://dx.doi.org/10.1021/acs.joc.7b00324.
Full textMaity, Soumitra, Injamam Ul Hoque, Saradindu Debnath, and Rabindranath Lo. "A Chromatographic Relay Conjugated Photoredox Strategy: S, Se- Pharmacophore from Alkenes via Formal [2+2+1] Heteroannulation." Chemical Communications, 2024. http://dx.doi.org/10.1039/d4cc03527e.
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