An efficient Stille cross-coupling reaction catalyzed by Pd(OAc)2/DAB-Cy catalytic system
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[1] Jaiwook Park,et al. One-pot synthesis of recyclable palladium catalysts for hydrogenations and carbon–carbon coupling reactions , 2004 .
[2] F. Diederich,et al. Book review: Metal-catalyzed cross-coupling reactions. F. Diederich and P. J. Stang (eds) Wiley–VCH, Weinheim, 1998. xxi + 517 pages, £85 ISBN 3–527–29421–X , 1998 .
[3] Jin‐Heng Li,et al. Dabco as an inexpensive and highly efficient ligand for palladium-catalyzed Suzuki-Miyaura cross-coupling reaction. , 2004, Organic letters.
[4] J. Serrano,et al. Palladacyclopentadiene Complexes with Mono- and Didentate Imidato Ligands: Synthesis, Hemilabile Behaviour and Catalytic Application in the Stille Reaction , 2004 .
[5] D. W. Boykin,et al. Simple amine/Pd(OAc)(2)-catalyzed suzuki coupling reactions of aryl bromides under mild aerobic conditions. , 2004, The Journal of organic chemistry.
[6] W. Su,et al. Pd2(dba)3/P(i-BuNCH2CH2)3N-catalyzed Stille cross-coupling of aryl chlorides. , 2004, Organic letters.
[7] J. Baldwin,et al. Stille coupling made easier-the synergic effect of copper(I) salts and the fluoride ion. , 2004, Angewandte Chemie.
[8] B. Arndtsen,et al. Imines in Stille-type cross-coupling reactions: a multicomponent synthesis of alpha-substituted amides. , 2004, Angewandte Chemie.
[9] F. West,et al. Improved yields with added copper(I) salts in carbonylative stille couplings of sterically hindered vinylstannanes. , 2004, The Journal of organic chemistry.
[10] S. Schneider,et al. Phospha-palladacycles and N-heterocyclic carbene palladium complexes: efficient catalysts for CC-coupling reactions☆ , 2003 .
[11] P. Vogel,et al. Palladium-catalyzed Stille cross-couplings of sulfonyl chlorides and organostannanes. , 2003, Journal of the American Chemical Society.
[12] Hyung-Jin Kim,et al. Regioselectivity in the Stille coupling reactions of 3,5-dibromo-2-pyrone. , 2003, Journal of the American Chemical Society.
[13] G. C. Fu,et al. Ligands for palladium-catalyzed cross-couplings of alkyl halides: use of an alkyldiaminophosphane expands the scope of the Stille reaction. , 2003, Angewandte Chemie.
[14] C. Wolf,et al. Efficient Stille cross-coupling reaction using aryl chlorides or bromides in water. , 2003, The Journal of organic chemistry.
[15] C. Wolf,et al. Use of highly active palladium-phosphinous acid catalysts in Stille, Heck, amination, and thiation reactions of chloroquinolines. , 2003, The Journal of organic chemistry.
[16] C. Amatore,et al. Mechanism of the Stille reaction catalyzed by palladium ligated to arsine ligand: PhPdI(AsPh3)(DMF) is the species reacting with vinylstannane in DMF. , 2003, Journal of the American Chemical Society.
[17] G. C. Fu,et al. Room-temperature Stille cross-couplings of alkenyltin reagents and functionalized alkyl bromides that possess beta hydrogens. , 2003, Journal of the American Chemical Society.
[18] Shu Yu,et al. Palladium(0)-catalyzed amination, Stille coupling, and Suzuki coupling of electron-deficient aryl fluorides. , 2003, Journal of the American Chemical Society.
[19] G. C. Fu,et al. Palladium-catalyzed coupling reactions of aryl chlorides. , 2002, Angewandte Chemie.
[20] A. Scrivanti,et al. Iminophosphine-palladium(0) Complexes as Catalysts for the Stille Reaction , 2002 .
[21] S. Nolan,et al. Catalytic cross-coupling reactions mediated by palladium/nucleophilic carbene systems , 2002 .
[22] W. Herrmann. N-heterocyclic carbenes: a new concept in organometallic catalysis. , 2002, Angewandte Chemie.
[23] M. Lemaire,et al. Aryl-aryl bond formation one century after the discovery of the Ullmann reaction. , 2002, Chemical reviews.
[24] J. Cintrat,et al. Stille cross-coupling reaction of an alpha-stannyl enamide. , 2001, The Journal of organic chemistry.
[25] R. Akiyama,et al. Microencapsulated Palladium Catalysts: Allylic Substitution and Suzuki Coupling Using a Recoverable and Reusable Polymer-Supported Palladium Catalyst This work was partially supported by a Grant-in-Aid for Scientific Research from the Ministry of Education, Science, Sports, and Culture, Japan. R.A. , 2001, Angewandte Chemie.
[26] S. Nolan,et al. Palladium/imidazolium salt catalyzed coupling of aryl halides with hypervalent organostannates. , 2001, Organic letters.
[27] Alonso,et al. Oxime Palladacycles: Stable and Efficient Catalysts for Carbon-Carbon Coupling Reactions. , 2000, Organic letters.
[28] Fu,et al. The First General Method for Stille Cross-Couplings of Aryl Chlorides. , 1999, Angewandte Chemie.
[29] T. Hiyama,et al. THE PALLADIUM-IMINOPHOSPHINE CATALYST FOR THE REACTIONS OF ORGANOSTANNANES , 1999 .
[30] D. Thompson,et al. Organometallics in synthesis , 1995 .
[31] R. Asselt,et al. Palladium complexes containing rigid bidentate nitrogen ligands as catalysts for carboncarbon bond formation , 1994 .
[32] John K. Stille,et al. The Palladium‐Catalyzed Cross‐Coupling Reactions of Organotin Reagents with Organic Electrophiles [New Synthetic Methods (58)] , 1986 .
[33] G. Gokel,et al. Phase-transfer-catalyzed Gomberg-Bachmann synthesis of unsymmetrical biarenes: a survey of catalysts and substrates , 1984 .
[34] L. N. Pridgen,et al. Regiospecific synthesis of arylfurans employing a nickel(II)-phosphine complex as a catalyst in the homolytic cross-coupling of Grignard reagents to halofurans , 1982 .
[35] J. Weir,et al. Palladium-catalyzed triethylammonium formate reductions. 4. Reduction of acetylenes to cis-monoenes and hydrogenolysis of tertiary allylic amines , 1980 .
[36] Marek P. Krzemiński,et al. The Cross-Coupling Reaction , 2005 .
[37] D. Harrowven. Handbook of Organopalladium Chemistry for Organic Synthesis , 2003 .
[38] K. Hoegenauer. trans-Di(μ-acetato)-bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) , 2001 .
[39] S. Lawrence,et al. Orthopalladated triaryl phosphite complexes as highly active catalysts in biaryl coupling reactions , 1998 .
[40] L. Pignolet. Homogeneous Catalysis with Metal Phosphine Complexes , 1983, Modern Inorganic Chemistry.
[41] J. Collman,et al. Principles and applications of organotransition metal chemistry , 1980 .