Copper-catalyzed cross-coupling of nonactivated secondary alkyl halides and tosylates with secondary alkyl Grignard reagents.
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[1] S. Bräse,et al. Metal-catalyzed cross-coupling reactions and more , 2014 .
[2] G. C. Fu,et al. New directing groups for metal-catalyzed asymmetric carbon-carbon bond-forming processes: stereoconvergent alkyl-alkyl Suzuki cross-couplings of unactivated electrophiles. , 2012, Journal of the American Chemical Society.
[3] T. Hatakeyama,et al. Tuning chemoselectivity in iron-catalyzed Sonogashira-type reactions using a bisphosphine ligand with peripheral steric bulk: selective alkynylation of nonactivated alkyl halides. , 2011, Angewandte Chemie.
[4] G. C. Fu,et al. Catalytic asymmetric γ-alkylation of carbonyl compounds via stereoconvergent Suzuki cross-couplings. , 2011, Journal of the American Chemical Society.
[5] Lei Liu,et al. Copper-catalyzed cross-coupling reaction of organoboron compounds with primary alkyl halides and pseudohalides. , 2011, Angewandte Chemie.
[6] R. Scopelliti,et al. A structure-activity study of Ni-catalyzed alkyl-alkyl Kumada coupling. Improved catalysts for coupling of secondary alkyl halides. , 2011, Journal of the American Chemical Society.
[7] B. Feringa,et al. Catalytic asymmetric carbon–carbon bond formation via allylic alkylations with organolithium compounds , 2011, Nature Chemistry.
[8] R. Jana,et al. Advances in transition metal (Pd, Ni, Fe)-catalyzed cross-coupling reactions using alkyl-organometallics as reaction partners. , 2011, Chemical reviews.
[9] A. Alexakis,et al. Identification of a valuable kinetic process in copper-catalyzed asymmetric allylic alkylation. , 2011, Angewandte Chemie.
[10] S. Buchwald,et al. Dialkylbiaryl Phosphines in Pd-Catalyzed Amination: A User's Guide. , 2010, Chemical science.
[11] A. Hoveyda,et al. Synthesis of quaternary carbon stereogenic centers through enantioselective Cu-catalyzed allylic substitutions with vinylaluminum reagents. , 2010, Journal of the American Chemical Society.
[12] G. C. Fu,et al. Asymmetric alkyl-alkyl cross-couplings of unactivated secondary alkyl electrophiles: stereoconvergent Suzuki reactions of racemic acylated halohydrins. , 2010, Journal of the American Chemical Society.
[13] G. C. Fu,et al. Asymmetric Suzuki cross-couplings of activated secondary alkyl electrophiles: arylations of racemic alpha-chloroamides. , 2010, Journal of the American Chemical Society.
[14] H. Takaya,et al. Iron-catalyzed Suzuki-Miyaura coupling of alkyl halides. , 2010, Journal of the American Chemical Society.
[15] G. Cahiez,et al. New Insights into the Copper-CatalyzedAlkylation of Grignard and Organolithium Reagents , 2010 .
[16] M. Lautens,et al. Secondary alkyl halides in transition-metal-catalyzed cross-coupling reactions. , 2009, Angewandte Chemie.
[17] D. Ma,et al. Copper/amino acid catalyzed cross-couplings of aryl and vinyl halides with nucleophiles. , 2008, Accounts of chemical research.
[18] A. Fürstner,et al. Preparation, structure, and reactivity of nonstabilized organoiron compounds. Implications for iron-catalyzed cross coupling reactions. , 2008, Journal of the American Chemical Society.
[19] M. Sai,et al. Copper-catalyzed reaction of alkyl halides with cyclopentadienylmagnesium reagent. , 2008, Organic letters.
[20] L. Sarandeses,et al. Enantioselective nickel-catalyzed cross-coupling reactions of trialkynylindium reagents with racemic secondary benzyl bromides. , 2008, Chemistry.
[21] Miguel García-Iglesias,et al. Ni-catalyzed cascade formation of C(sp3)--C(sp3) bonds by cyclization and cross-coupling reactions of iodoalkanes with alkyl zinc halides. , 2007, Angewandte Chemie.
[22] G. Asensio,et al. Palladium-catalyzed Suzuki-Miyaura reaction involving a secondary sp3 carbon: studies of stereochemistry and scope of the reaction. , 2007, Chemistry.
[23] N. Kambe,et al. Copper-catalyzed cross-coupling reaction of grignard reagents with primary-alkyl halides: remarkable effect of 1-phenylpropyne. , 2007, Angewandte Chemie.
[24] M. Lautens,et al. Stereochemical and mechanistic investigations of a palladium-catalyzed annulation of secondary alkyl iodides. , 2007, Angewandte Chemie.
[25] P. Pulay,et al. Ligand redox effects in the synthesis, electronic structure, and reactivity of an alkyl-alkyl cross-coupling catalyst. , 2006, Journal of the American Chemical Society.
[26] F. Glorius,et al. The first palladium-catalyzed Sonogashira coupling of unactivated secondary alkyl bromides , 2006 .
[27] G. C. Fu,et al. Amino alcohols as ligands for nickel-catalyzed suzuki reactions of unactivated alkyl halides, including secondary alkyl chlorides, with arylboronic acids. , 2006, Journal of the American Chemical Society.
[28] H. Ohmiya,et al. Cobalt(diamine)-catalyzed cross-coupling reaction of alkyl halides with arylmagnesium reagents: stereoselective constructions of arylated asymmetric carbons and application to total synthesis of AH13205. , 2006, Journal of the American Chemical Society.
[29] Christian Herber,et al. Enantioselective total synthesis and determination of the absolute configuration of the 4,6,8,10,16,18-hexamethyldocosane from Antitrogus parvulus. , 2007, Angewandte Chemie.
[30] M. Beller,et al. Catalysts for cross-coupling reactions with non-activated alkyl halides. , 2005, Angewandte Chemie.
[31] I. Beletskaya,et al. Copper in cross-coupling reactions: The post-Ullmann chemistry , 2004 .
[32] H. Ohmiya,et al. Cobalt-catalyzed cross-coupling reactions of alkyl halides with allylic and benzylic Grignard reagents and their application to tandem radical cyclization/cross-coupling reactions. , 2004, Chemistry.
[33] A. Fürstner,et al. Cross-coupling of alkyl halides with aryl grignard reagents catalyzed by a low-valent iron complex. , 2004, Angewandte Chemie.
[34] E. Nakamura,et al. Iron-catalyzed cross-coupling of primary and secondary alkyl halides with aryl grignard reagents. , 2004, Journal of the American Chemical Society.
[35] G. C. Fu,et al. Cross-couplings of unactivated secondary alkyl halides: room-temperature nickel-catalyzed Negishi reactions of alkyl bromides and iodides. , 2003, Journal of the American Chemical Society.
[36] N. Kambe,et al. Ni- or Cu-catalyzed cross-coupling reaction of alkyl fluorides with Grignard reagents. , 2003, Journal of the American Chemical Society.
[37] H. Yorimitsu,et al. Cobalt-catalyzed coupling reaction of alkyl halides with allylic grignard reagents. , 2002, Angewandte Chemie.
[38] H. Yorimitsu,et al. Cobalt-catalyzed tandem radical cyclization and cross-coupling reaction: its application to benzyl-substituted heterocycles. , 2001, Journal of the American Chemical Society.
[39] G. Cahiez,et al. Cu-Catalyzed Alkylation of Grignard Reagents: A New Efficient Procedure , 2000 .
[40] B. Lipshutz. Downsizing Copper in Modern Cuprate Couplings , 1997 .
[41] Jeffrey D. Miller,et al. Scope and Utility of a New Soluble Copper Catalyst [CuBr−LiSPh−LiBr−THF]: A Comparison with Other Copper Catalysts in Their Ability to Couple One Equivalent of a Grignard Reagent with an Alkyl Sulfonate , 1997 .
[42] P. Knochel,et al. A New Nickel‐Catalyzed Cross‐Coupling Reaction between sp3 Carbon Centers , 1996 .
[43] N. Miyaura,et al. Palladium-Catalyzed Alkyl-Alkyl Cross-Coupling Reaction of 9-Alkyl-9-BBN Derivatives with Iodoalkanes Possessing β-Hydrogens. , 1992 .
[44] E. Nakamura,et al. Copper-catalyzed reactions of organotitanium reagents. Highly SN2'- and anti-selective and diastereo- and chemoselective alkylation of allylic chlorides and phosphates , 1991 .
[45] Yasushi Kawai,et al. Stereochemical control of microbial reduction. 17. A method for controlling the enantioselectivity of reductions with bakers' yeast , 1991 .
[46] J. Kochi,et al. Copper-catalyzed coupling of grignard reagents and akyl halides in tetrahydrofuran solutions , 1972 .
[47] J. Kochi,et al. Mechanism of the silver-catalyzed reaction of Grignard reagents with alkyl halides , 1971 .