A general and selective copper-catalyzed cross-coupling of tertiary Grignard reagents with azacyclic electrophiles.
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[1] Shijie Ren,et al. New optoelectronic materials based on bitriazines: synthesis and properties. , 2008, Organic letters.
[2] D. Natale,et al. The combination of transition metal ions and hydrogen-bonding interactions. , 2008, Chemical communications.
[3] A. Cooksy,et al. Hydrogen-bond acceptance of bifunctional ligands in an alkyne-metal pi complex. , 2008, Journal of the American Chemical Society.
[4] Lukas Hintermann,et al. Expedient syntheses of the N-heterocyclic carbene precursor imidazolium salts IPr·HCl, IMes·HCl and IXy·HCl , 2007, Beilstein journal of organic chemistry.
[5] L. Zani,et al. Redox-neutral synthesis of beta-amino aldehydes from imines by an alkynylation/hydration sequence. , 2007, The Journal of organic chemistry.
[6] De‐Xian Wang,et al. Formation and conformational conversion of flattened partial cone oxygen bridged calix[2]arene[2]triazines. , 2007, Organic letters.
[7] Lukas Hintermann,et al. Catalytic Hydration of Alkynes and Its Application in Synthesis , 2007 .
[8] Y. Naitoh,et al. Cross-coupling of alkyl halides with Grignard reagents using nickel and palladium complexes bearing eta(3)-allyl ligand as catalysts. , 2007, Chemical communications.
[9] M. Rueping,et al. A manganese-catalyzed cross-coupling reaction , 2007 .
[10] B. Tekwani,et al. Synthesis, antimalarial, antileishmanial, antimicrobial, cytotoxicity, and methemoglobin (MetHB) formation activities of new 8-quinolinamines. , 2007, Bioorganic & Medicinal Chemistry.
[11] Lukas Hintermann,et al. Highly active in situ catalysts for anti-Markovnikov hydration of terminal alkynes. , 2006, Organic letters.
[12] T. Schall,et al. Optimization of 2-aminothiazole derivatives as CCR4 antagonists. , 2006, Bioorganic & medicinal chemistry letters.
[13] R. Olsson,et al. Iron-catalyzed cross-coupling of imidoyl chlorides with Grignard reagents. , 2006, Organic letters.
[14] A. Kling,et al. Synthesis and SAR of highly potent and selective dopamine D3-receptor antagonists: 1H-Pyrimidin-2-one derivatives , 2006 .
[15] D. Grotjahn. Bifunctional organometallic catalysts involving proton transfer or hydrogen bonding. , 2005, Chemistry.
[16] M. Organ,et al. The first Negishi cross-coupling reaction of two alkyl centers utilizing a Pd-N-heterocyclic carbene (NHC) catalyst. , 2005, Organic letters.
[17] C. Stock,et al. Regioselective Cross-Coupling Reactions of Multiple Halogenated Nitrogen-, Oxygen-, and Sulfur-Containing Heterocycles , 2005 .
[18] M. Beller,et al. Katalysatoren machen's möglich: Selektive C‐C‐Kupplungen mit nichtaktivierten Alkylhalogeniden , 2005 .
[19] M. Beller,et al. Catalysts for cross-coupling reactions with non-activated alkyl halides. , 2005, Angewandte Chemie.
[20] G. C. Fu,et al. Nickel‐Catalyzed Cross‐Couplings of Unactivated Alkyl Halides and Pseudohalides with Organometallic Compounds , 2004 .
[21] D. Yamazaki,et al. Pyrimidine-core extended pi-systems: general synthesis and interesting fluorescent properties. , 2004, Journal of the American Chemical Society.
[22] D. Grotjahn,et al. A general bifunctional catalyst for the anti-Markovnikov hydration of terminal alkynes to aldehydes gives enzyme-like rate and selectivity enhancements. , 2004, Journal of the American Chemical Society.
[23] B. Scheiper,et al. Selective iron-catalyzed cross-coupling reactions of grignard reagents with enol triflates, acid chlorides, and dichloroarenes. , 2004, The Journal of organic chemistry.
[24] M. Beer,et al. Thiazoles and thiopyridines: novel series of high affinity h5HT(7) ligands. , 2004, Bioorganic & medicinal chemistry letters.
[25] Diego J. Cárdenas. Metall‐katalysierte Alkyl‐Alkyl‐Kreuzkupplungen in Gegenwart funktioneller Gruppen , 2003 .
[26] D. Cárdenas. Advances in functional-group-tolerant metal-catalyzed alkyl-alkyl cross-coupling reactions. , 2003, Angewandte Chemie.
[27] Adam F. Littke,et al. Palladiumkatalysierte Kupplungen von Arylchloriden , 2002 .
[28] G. C. Fu,et al. Palladium-catalyzed coupling reactions of aryl chlorides. , 2002, Angewandte Chemie.
[29] A. Fürstner,et al. Iron-catalyzed cross-coupling reactions. , 2002, Journal of the American Chemical Society.
[30] J. Duan,et al. β-Carbolines as specific inhibitors of cyclin-Dependent kinases , 2002 .
[31] N. Kambe,et al. Nickel-catalyzed cross-coupling reaction of grignard reagents with alkyl halides and tosylates: remarkable effect of 1,3-butadienes. , 2002, Journal of the American Chemical Society.
[32] M. Lemaire,et al. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction. , 2002, Chemical reviews.
[33] G. Rowlands. Ambifunctional Cooperative Catalysts , 2001 .
[34] A. Itai,et al. Retinoidal pyrimidinecarboxylic acids. Unexpected diaza-substituent effects in retinobenzoic acids. , 2000, Chemical & pharmaceutical bulletin.
[35] H. Jacobsen,et al. The Chemistry of New Nitrosyltungsten Complexes with Pyridyl‐Functionalized Phosphane Ligands , 2000 .
[36] W. Herrmann,et al. Eine Nickel-katalysierte Kreuzkupplung von Arylchloriden mit Aryl-Grignard-Reagentien , 2000 .
[37] W. Herrmann,et al. Nickel-Catalyzed Cross-Coupling of Aryl Chlorides with Aryl Grignard Reagents N-Heterocyclic Carbenes, Part 27. This work was supported by Aventis R&T, the Deutsche Forschungsgemeinschaft (DFG), the Bayerischer Forschungsverbund Katalyse (FORKAT), Degussa-Hüls AG, and the Fonds der Chemischen Indust , 2000, Angewandte Chemie.
[38] B. Ziemer,et al. A Facile Route to Bridgehead Disubstituted Bicyclo[1.1.1]pentanes Involving Palladium‐Catalyzed Cross‐Coupling Reactions , 1999 .
[39] G. Cahiez,et al. Highly Stereo- and Chemoselective Iron-Catalyzed Alkenylation of Organomagnesium Compounds , 1998 .
[40] C. Bolm,et al. Transition Metals for Organic Synthesis , 1998 .
[41] G. Koten,et al. Novel tridentate diamino organomanganese(II) complexes as homogeneous catalysts in manganese(II)/copper(I) catalyzed carbon-carbon bond forming reactions , 1998 .
[42] A. Holý,et al. Coupling of 6-chloropurines with organocuprates derived from grignard reagents: A convenient route to sec and tert 6-alkylpurines , 1996 .
[43] N. Kanomata,et al. Nucleophilic radical substitution of polychloroazines , 1993 .
[44] P. Gallagher,et al. Synthesis of 6-tert-Butyl-2-Arylpyridines , 1992 .
[45] P. Gallagher,et al. Novel immunosuppressive butenamides , 1992 .
[46] Georg Kottirsch,et al. Nickel(0)‐katalysierte Kupplung von (Tricyclo[4.1.0.02,7]hept‐1‐yl)‐magnesiumbromid und verwandten Grignard‐Verbindungen mit Aryl‐, Vinyl‐ und Alkinylhalogeniden , 1990 .
[47] R. F. Evans,et al. The synthesis of 4(6)-t-butylpyrimidines from 4(6)-halopyrimidines by using higher-order lithium and magnesium organocuprate reagents , 1990 .
[48] A. Shirahata. Novel and facile syntheses of t-butyl substituted silanes from t-butyl magnesium chloride and chlorosilanes catalyzed by cuprous cyanide , 1989 .
[49] K. Polborn,et al. 8,8'-Bis[tetracyclo[5.1.0.01,6.02,7]octane], a coupled [1.1.1]propellane: synthesis and structure , 1988 .
[50] S. V. Patel,et al. Alkylation of heteroaryl halides by 2:1 Grignard reagent/copper(I) mixtures. Synthesis of alkylated octahydrodibenzo[b,j][1,10]phenanthrolines , 1987 .
[51] S. Berger,et al. Strained benzene derivatives by copper-catalyzed tert-butylation , 1985 .
[52] M. Kumada,et al. CROSS-COUPLING OF TERTIARY ALKYL GRIGNARD REAGENTS WITH β-BROMOSTYRENE CATALYZED BY DICHLORO[1,1′-BIS(DIPHENYLPHOSPHINO)FERROCENE]NICKEL(II) , 1980 .
[53] R. S. Smith,et al. Mechanistic studies of iron catalysis in the cross coupling of alkenyl halides and Grignard reagents , 1976 .
[54] J. Kochi,et al. Synthesis of olefins. Cross-coupling of alkenyl halides and Grignard reagents catalyzed by iron complexes , 1975 .
[55] J. Dubois,et al. Condensation chlorure d'acide-organomagnesien en presence d'halogenure cuivreux: Competition des reactions heterolytique et homolytique. synthese de cetones aliphatiques ramifiees , 1973 .
[56] K. Tamao,et al. Alkyl group isomerization in the cross-coupling reaction of secondary alkyl Grignard reagents with organic halides in the presence of nickel-phosphine complexes as catalysts , 1972 .
[57] J. Dubois,et al. Investigation of optimal conditions for the synthesis of hindered aliphatic ketones. Catalytic orientation of the condensation of RLi or RMgX- R'COCl by cuprous halides. , 1971 .
[58] P. Gould,et al. 195. Some substituted 1,3,5-triazines , 1965 .