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Download Oxidative Cross-Coupling Reactions by Aiwen Lei, Wei Shi, Chao Liu, Wei Liu, Hua Zhang, Chuan He PDF

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By Aiwen Lei, Wei Shi, Chao Liu, Wei Liu, Hua Zhang, Chuan He

The 1st instruction manual in this rising box presents a entire evaluate of transition metal-catalyzed coupling reactions within the presence of an oxidant. Following an advent to the final thought and mechanism of this response classification, the staff of authors provides chapters on C-C cross-coupling reactions utilizing organometallic companions, C-Heteroatom bond forming reactions through oxidative couplings, and C-H couplings through C-H activation. The textual content additionally covers such groundbreaking issues as fresh achievements within the fields of C-C and C-X bond formation reactions in addition to C-H activation concerning oxidative couplings.
With its novel and concise technique in the direction of very important development blocks in natural chemistry and its concentrate on artificial functions, this instruction manual is of serious curiosity to all man made chemists in academia and alike.

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And Jutand, A. (2008) Eur. J. Org. , 2008, 4567–4570. F. (2007) Chin. Chem. , 18, 1043–1046. Yamamoto, Y. (2007) Synlett, 1913–1916. , and Zhang, Y. (2007) Catal. , 9, 97–100. , and Tsukuda, T. (2007) J. Organomet. , 692, 368–374. 103. , and Zhang, Y. 104. 105. 106. 107. 108. 109. 110. 111. 112. 113. 114. 115. 116. 117. 118. 119. 120. 121. (2007) J. Mol. Catal. , 273, 240–243. , and Tao, X. (2006) Cuihua Xuebao, 27, 1051–1052. , and Corma, A. (2005) Angew. Chem. Int. , 44, 2242–2245. M. E. , 44, 765–768.

5 equiv. 5 equiv. or less excess could also achieve good selectivity). 27, 20 mol% of MnCl2 ⋅2LiCl was employed as the catalyst, and cross-coupled products were obtained in satisfactory yields. Later, Studer et al. reported transition-metal-free cross-coupling between aryl, alkenyl, and alkynyl magnesium compounds using TEMPO as the oxidant [49]. 28. 5 equiv. 85 equiv. in excess. 29. 27 Manganese-catalyzed oxidative cross-coupling between aryl and alkynyl Grignard reagents. 2 Ar 2R Ar MgX TEMPO,THF 5–30 min, reflux MgX MgX + R Ar TEMPO,THF R 4–6 h, reflux MgX Ar TEMPO R Ar R ?

2009) Eur. J. Org. , 2009, 1864–1867. G. and Guzman, J. (2008) Appl. Catal. A, 339, 68–75. Vogler, T. and Studer, A. (2008) Adv. Synth. , 350, 1963–1967. , and Tanaka, H. , 49, 6593–6595. G. (2008) J. Mol. Catal. , 285, 14–19. , and Jutand, A. (2008) Eur. J. Org. , 2008, 4567–4570. F. (2007) Chin. Chem. , 18, 1043–1046. Yamamoto, Y. (2007) Synlett, 1913–1916. , and Zhang, Y. (2007) Catal. , 9, 97–100. , and Tsukuda, T. (2007) J. Organomet. , 692, 368–374. 103. , and Zhang, Y. 104. 105. 106. 107.

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