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    Source: Proceedings of the National Academy of Sciences of Belarus, Chemical Series; № 4 (2015); 34-41 ; Известия Национальной академии наук Беларуси. Серия химических наук; № 4 (2015); 34-41 ; 2524-2342 ; 1561-8331 ; undefined

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    Relation: https://vestichem.belnauka.by/jour/article/view/152/152; Transition Metal-Catalyzed Cross-Coupling Reactions: monograph. Ed. F. Diederich, P. J. Stang. - New York: Wiley-VCH, 1998. - P. 1-229.; Topics in Current Chemistry - Cross-Coupling Reactions: monograph. Ed N. Miyaura. - Heidelberg: Springer, 2002. -Vol. 219. - Р. 1-241.; Handbook of Organopalladium Chemistry for Organic Synthesis: monograph. Ed E-i. Negishi. - New York: John Wiley and Sons, 2002. - Vol. 1. - Р. 213-589.; Beletskaya, I. P. The Heck Reaction as a Sharpening Stone of Palladium Catalysis / I. P. Beletskaya, A. V. Cheprakov // Chem. Rev. - 2000. - Vol. 100, № 8. - P. 3009-3066.; Supported palladium catalysts for fine chemicals synthesis / H.-U. Blaser [et al.] // J. Mol. Catal. A: Chem. - 2001. -Vol. 173, № 1. - P. 3-18.; Organometallics in Process Chemistry: monograph. Ed. R. D. Larsen. - Berlin: Springer, 2004. - P. 205-245.; Chinchilla, R. The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry / R. Chinchilla, C. Najera // Chem. Rev. - 2007. - Vol. 107, № 3. - P. 874-922.; De Vries, J. G. The Heck reaction in the production of fine chemicals / J. G. de Vries // Can. J. Chem. - 2001. - Vol. 79, № 5-6. - P. 1086-1092.; Barnard, C. Challenges in Catalysis for Pharmaceuticals and Fine Chemicals / C. Barnard // Platinum Metals Rev. -2008. - Vol. 52, № 2. - P. 110-113.; Chinchilla, R. Metalated heterocycles in organic synthesis: Recent applications / R. Chinchilla, C. Najera, M. Yus // Arkivoc. - 2007. - Vol. 2007, № 1. - P. 152-231.; Sasaki, M. Total Synthesis of Polycyclic Ether Natural Products Based on Suzuki-Miyaura Cross-Coupling / M. Sasaki, H. Fuwa // Synlett. - 2004. - № 11. - P. 1851-1874.; Nicolaou, K. C. Palladium-catalyzed cross-coupling reactions in total synthesis / K. C. Nicolaou, P. G. Bulger, D. Sarlah // Angew. Chem. Int. Ed. - 2005. - Vol. 44, № 29. - P. 4442-4489.; Roglans, A. Diazonium Salts as Substrates in Palladium-Catalyzed Cross-Coupling Reactions / A. Roglans, A. Pla-Quintana, M. Moreno-Manas // Chem. Rev. - 2006. - Vol. 106, № 11.- P. 4622-4643.; Yin, L. Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts / L. Yin, J. Liebscher // Chem. Rev. - 2007. - Vol. 107, № 1. - P. 133-173.; Замещенные n-[изоксазол(изотиазол)-3-ил(метилен)метил] ариламины: синтез, комплексы с палладием и их каталитическая активность в водных средах / А. В. Клецков [и др.] // Вес. Нац. акад. навук Беларуси Сер. хiм. навук. -2015. - № 2. - С. 54-62.; Синтез и каталитическая активность новых комплексов палладия(П) с замещенными изоксазольными и изотиазольными лигандами / Н. А. Бумагин [и др.] // Докл. Нац. акад. навук Беларуси 2015. - Т. 59, № 2. - С. 72-78.; Bumagin, N. A. Ligandless palladium catalyzed reactions of arylboronic acids and sodium tetraphenylborate with aryl halides in aqueous media / N. A. Bumagin, V. V. Bykov // Tetrahedron. - 1997. - Vol. 53, № 42. - P. 14437-14450.; Crystalline mesoporous g-Al2O3 supported palladium: Novel and efficient catalyst for Suzuki-Miyaura reaction under controlled microwave heating / G. Feng [et al.] // Catal. Commun. - 2013. - Vol. 37, № 1. - P. 27-31.; https://vestichem.belnauka.by/jour/article/view/152; undefined

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