cine Substitution and the Cu Effect in Stille Cross‐Coupling Reactions: Mechanistic Perspectives and Synthetic Utility

cine Substitution arising from slow transmetallation occasionally occurs in classic Pd-catalyzed Stille cross-coupling reactions with sterically hindered vinyltin components. Mechanistic explanations of this "abnormal" cross-coupling mode and the intriguing co-catalytic effects of metallic Cu species in restoring the ipso selectivity are summarized. Typical synthetic applications of this unique Cu effect and the advent of Cu-catalyzed Stille-type cross-coupling are also demonstrated.

[1]  Jean‐Claude Kizirian,et al.  α‐ and β‐Stannyl Trifluoromethylbutenoates: Regioselective Preparation and Use in Copper(I)‐Catalyzed Allylation and Propargylation Reactions , 2010 .

[2]  Alena Rudolph,et al.  Sekundäre Alkylhalogenide in übergangsmetallkatalysierten Kreuzkupplungen , 2009 .

[3]  G. C. Fu The development of versatile methods for palladium-catalyzed coupling reactions of aryl electrophiles through the use of P(t-Bu)3 and PCy3 as ligands. , 2008, Accounts of chemical research.

[4]  A. Basso,et al.  Multicomponent synthesis of benzoxazinones via tandem Ugi/Mitsunobu reactions: an unexpected cine-substitution , 2008, Molecular Diversity.

[5]  A. Lera,et al.  Associative Transmetalation in the Stille Cross-Coupling Reaction to Form Dienes: Theoretical Insights into the Open Pathway , 2008 .

[6]  H. Zuilhof,et al.  Photochemical generation and reactivity of naphthyl cations : cine substitution , 2007 .

[7]  A. de Meijere,et al.  Stille-Heck coupling sequences applied in a versatile new access to steroid skeletons. , 2007, Chemistry.

[8]  B. Stoltz,et al.  The development and scope of a versatile tandem Stille-oxa-electrocyclization reaction , 2007 .

[9]  Zhenyang Lin,et al.  Effect of the Leaving Ligand X on Transmetalation of Organostannanes (vinylSnR3) with LnPd(Ar)(X) in Stille Cross-Coupling Reactions. A Density Functional Theory Study , 2006 .

[10]  A. Lledós,et al.  A critical analysis of the cyclic and open alternatives of the transmetalation step in the stille cross-coupling reaction. , 2006, Journal of the American Chemical Society.

[11]  R. L. Funk,et al.  A strategy for the total synthesis of dragmacidin E. Construction of the core ring system. , 2006, Organic letters.

[12]  Y. Matsuo,et al.  Synthesis of ent-thallusin. , 2006, Organic letters.

[13]  Michael S. Wilson,et al.  A synthetic approach toward nitiol: construction of two 1,22-dihydroxynitianes. , 2006, The Journal of organic chemistry.

[14]  P. Baran,et al.  Total synthesis of (+/-)-haouamine A. , 2006, Journal of the American Chemical Society.

[15]  Yi Wang,et al.  Copper(I)-only catalyzed reactions of (E)-2,3-difluoro-3-stannylacrylic ester with acid chlorides and mechanistic studies of the "copper effect" in stille coupling reactions. , 2006, Organic letters.

[16]  R. S. Coleman,et al.  Total synthesis of strobilurin B using a hetero-bis-metallated pentadiene linchpin. , 2006, Chemical communications.

[17]  R. Álvarez,et al.  Computational characterization of a complete palladium-catalyzed cross-coupling process: the associative transmetalation in the Stille reaction. , 2006, Organic letters.

[18]  M. Willis,et al.  A new reactivity pattern for vinyl bromides: cine-substitution via palladium catalysed C-N coupling/Michael addition reactions. , 2005, Organic & biomolecular chemistry.

[19]  K. Nicolaou,et al.  Palladiumkatalysierte Kreuzkupplungen in der Totalsynthese , 2005 .

[20]  Aubry K. Miller,et al.  Biomimetic synthesis of elysiapyrones A and B. , 2005, Organic letters.

[21]  J. Baldwin,et al.  Significant enhancement of the Stille reaction with a new combination of reagents-copper(I) iodide with cesium fluoride. , 2005, Chemistry.

[22]  Aubry K. Miller,et al.  Stereoselective synthesis of cyercene A and the placidenes. , 2005, Organic letters.

[23]  F. Nigsch,et al.  Total synthesis of (+)-crocacin D. , 2005, The Journal of organic chemistry.

[24]  J. Rainier,et al.  The total synthesis of gambierol. , 2005, Journal of the American Chemical Society.

[25]  M. Beller,et al.  Katalysatoren machen's möglich: Selektive C‐C‐Kupplungen mit nichtaktivierten Alkylhalogeniden , 2005 .

[26]  I. Beletskaya,et al.  Copper in cross-coupling reactions: The post-Ullmann chemistry , 2004 .

[27]  A. Echavarren,et al.  Die Mechanismen der Stille‐Reaktion , 2004 .

[28]  D. Lupton,et al.  Synthesis of quinolines, 2-quinolones, phenanthridines, and 6(5h)-phenanthridinones via palladium[0]-mediated Ullmann cross-coupling of 1-bromo-2-nitroarenes with beta-halo-enals, -enones, or -esters. , 2004, Organic letters.

[29]  N. Powell,et al.  Total synthesis of formamicin. , 2004, Journal of the American Chemical Society.

[30]  M. Belema,et al.  Synthesis of 1,1-diarylethylenes from an α-stannyl β-silylstyrene , 2004 .

[31]  A. D. Meijere,et al.  Synthese substituierter Steroide und Steroidanaloga durch Stille‐Heck‐Kupplungssequenzen , 2004 .

[32]  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.

[33]  N. Taylor,et al.  Cine-substitution in the Stille coupling: evidence for the carbenoid reactivity of sp3-gem-organodimetallic iodopalladio-trialkylstannylalkane intermediates. , 2003, Journal of the American Chemical Society.

[34]  Okanya J. Kokas,et al.  Synthesis of indoles via palladium[0]-mediated Ullmann cross-coupling of o-halonitroarenes with alpha-halo-enones or -enals. , 2003, Organic letters.

[35]  S. Buchwald,et al.  Ipso- or cine-substitutions of 6-haloimidazo[1,2-a]pyridine derivatives with different azoles depending on the reaction conditions. , 2003, The Journal of organic chemistry.

[36]  P. Espinet,et al.  Quantitative Evaluation of the Factors Contributing to the “Copper Effect” in the Stille Reaction , 2003 .

[37]  Tamio Hayashi,et al.  A new cine-substitution of alkenyl sulfones with aryltitanium reagents catalyzed by rhodium: mechanistic studies and catalytic asymmetric synthesis of allylarenes. , 2003, Journal of the American Chemical Society.

[38]  Diego J. Cárdenas Metall‐katalysierte Alkyl‐Alkyl‐Kreuzkupplungen in Gegenwart funktioneller Gruppen , 2003 .

[39]  W. Roush,et al.  Total synthesis of the formamicin aglycon, formamicinone. , 2003, Organic letters.

[40]  Yoshinori Yamamoto,et al.  Total synthesis of gambierol. , 2003, Journal of the American Chemical Society.

[41]  G. Salas,et al.  14-Electron T-shaped [PdRXL] complexes: evidence or illusion? Mechanistic consequences for the stille reaction and related processes. , 2002, Chemistry.

[42]  James C. Anderson,et al.  The direct use of phenyldimethylsilanes in silicon assisted palladium catalysed cross coupling. , 2002, Chemical communications.

[43]  M. Satake,et al.  Total synthesis of gambierol. , 2002, Organic letters.

[44]  L. Overman,et al.  Enantioselective total synthesis of quadrigemine C and psycholeine. , 2002, Journal of the American Chemical Society.

[45]  M. Kosugi,,et al.  A historical note of the Stille reaction , 2002 .

[46]  G. Pattenden,et al.  The intramolecular Stille reaction in some target natural product syntheses , 2002 .

[47]  G. C. Fu,et al.  Pd/P(t-Bu)(3): a mild and general catalyst for Stille reactions of aryl chlorides and aryl bromides. , 2002, Journal of the American Chemical Society.

[48]  M. Lemaire,et al.  Aryl-aryl bond formation one century after the discovery of the Ullmann reaction. , 2002, Chemical reviews.

[49]  Julia Schuppan,et al.  Synthese von Apoptolidinon , 2001 .

[50]  J. Suwiński,et al.  cine- and tele-Substitution Reactions , 2001 .

[51]  U. Kazmaier,et al.  Preparation and reactions of stannylated amino acids. , 2001, Chemistry.

[52]  David R. Williams,et al.  Total synthesis of (+)-amphidinolide K. , 2001, Journal of the American Chemical Society.

[53]  P. Espinet,et al.  Snapshots of a Stille reaction , 2001 .

[54]  A. M. Gallego,et al.  Mechanism of the Stille Reaction. 2. Couplings of Aryl Triflates with Vinyltributyltin. Observation of Intermediates. A More Comprehensive Scheme , 2000 .

[55]  E. Corey,et al.  Enantioselective Total Synthesis of Nicandrenones , 2000 .

[56]  E. Corey,et al.  Cuprous Chloride Accelerated Stille Reactions. A General and Effective Coupling System for Sterically Congested Substrates and for Enantioselective Synthesis , 1999 .

[57]  I. Paterson,et al.  Total Synthesis of Elaiolide Using a Copper(I)-Promoted Stille Cyclodimerization Reaction , 1999 .

[58]  P. Espinet,et al.  Mechanism of the Stille Reaction. 1. The Transmetalation Step. Coupling of R1I and R2SnBu3 Catalyzed by trans-[PdR1IL2] (R1 = C6Cl2F3; R2 = Vinyl, 4-Methoxyphenyl; L = AsPh3) , 1998 .

[59]  A. Flohr Stille coupling versus cine substitution. Electronic effects also influence coupling sterically hindered stannanes , 1998 .

[60]  Jean‐Francois Betzer STILLE COUPLING REACTIONS IN THE PREPARATION OF SUBSTITUTED TRIENIC SYSTEMS , 1998 .

[61]  P. Espinet,et al.  ON THE CONFIGURATION RESULTING FROM OXIDATIVE ADDITION OF RX TO PD(PPH3)4 AND THE MECHANISM OF THE CIS-TO-TRANS ISOMERIZATION OF PDRX(PPH3)2 COMPLEXES (R = ARYL, X = HALIDE) , 1998 .

[62]  C. Urch,et al.  On the cine substitution of 1,1-bis(tri-n-butylstannyl)ethenes in an intramolecular Stille reaction , 1998 .

[63]  T. Choshi,et al.  THE ANOMALOUS STILLE REACTION OF 5-STANNYLIMIDAZOLE WITH 3-IODOINDOLE , 1998 .

[64]  J. Šrogl,et al.  Sulfonium Salts. Participants par Excellence in Metal-Catalyzed Carbon−Carbon Bond-Forming Reactions , 1997 .

[65]  Shu‐Hui Chen,et al.  On the Stille vinylation reactions with α-styryltrimethyltin , 1997 .

[66]  Dawei Zhang,et al.  Ambient Temperature, Ullmann-like Reductive Coupling of Aryl, Heteroaryl, and Alkenyl Halides. , 1997, The Journal of organic chemistry.

[67]  I. Paterson,et al.  Studies in macrolide synthesis: A novel cyclodimerisation approach to the synthesis of elaiophylin using a double Stille cross-coupling reaction , 1997 .

[68]  V. Farina,et al.  On the mechanism of cine substitution in the Stille reaction: New evidence for the intermediacy of Pd(0) carbenes , 1996 .

[69]  K. Nicolaou,et al.  Kupfer(I)‐unterstützte Stille‐Kupplung von α‐stannylsubstituierten Enolethern mit Enoltriflaten: Aufbau von komplexen Polyethergerüsten , 1996 .

[70]  G. D. Allred,et al.  Copper-Mediated Cross-Coupling of Organostannanes with Organic Iodides at or below Room Temperature , 1996 .

[71]  V. Farina New perspectives in the cross-coupling reactions of organostannanes , 1996 .

[72]  J. Witherington,et al.  Pd/Cu Co-catalysed Cross-coupling Reactions of Methyl (Z)-2-Tributylstannyl-3-methoxypropenoate: a Method for Direct Introduction of the Agrochemically Important β-Methoxyacrylate Toxophore , 1995 .

[73]  Robert E. Johnson,et al.  The Anomalous Stille Reactions of Methyl .alpha.-(Tributylstannyl)acrylate: Evidence for a Palladium Carbene Intermediate , 1994 .

[74]  S. Kapadia,et al.  On the Nature of the "Copper Effect" in the Stille Cross-Coupling , 1994 .

[75]  G. Crisp,et al.  Elaboration of the side chain of α-amino acids by palladium-catalysed stille couplings , 1994 .

[76]  T. Hiyama,et al.  On the regioselectivity of palladium catalyzed cross-coupling reactions of alkenylsilanes : participation of β-cationic organosilicate-palladium species during the transmetallation , 1994 .

[77]  C. Amatore,et al.  Intimate mechanism of oxidative addition to zerovalent palladium complexes in the presence of halide ions and its relevance to the mechanism of palladium-catalyzed nucleophilic substitutions , 1993 .

[78]  J. Levin Palladium-catalyzed coupling of an α-stannyl acrylate to aryl iodides and triflates. A one-step synthesis of aryl propenoic esters. , 1993 .

[79]  Koichiro Watanabe,et al.  A simple and efficient synthesis of 2,- 3-, or 4-(2-nitrophenyl)pyridine derivatives via palladium catalyzed ullmann cross-coupling reaction , 1993 .

[80]  W. O. Moss,et al.  Internal coordination at tin promotes selective alkyl transfer in the Stille coupling reaction , 1992 .

[81]  T. Mitchell Palladium-Catalysed Reactions of Organotin Compounds , 1992 .

[82]  G. Crisp,et al.  Synthesis of Modified Nucleosides. Palladium-Catalysed Couplings of Organostannanes or Organoboranes with Pyrimidine Nucleosides , 1991 .

[83]  G. Stork,et al.  Cine substitution in vinylstannane cross-coupling reactions , 1990 .

[84]  L. S. Liebeskind,et al.  3-Stannylcyclobutenediones as nucleophilic cyclobutenedione equivalents. Synthesis of substituted cyclobutenediones and cyclobutenedione monoacetals and the beneficial effect of catalytic copper iodide on the Stille reaction , 1990 .

[85]  K. Kikukawa,et al.  A First Palladium-Catalyzed Aryldegermylation of Styryltrimethylgermanes , 1990 .

[86]  T. L. Gilchrist,et al.  Abnormal products of palladium catalysed coupling reactions of (1-bromovinyl)trimethylsilane , 1989 .

[87]  J. Marino,et al.  New strategies for annulations: a highly convergent and stereoselective synthesis of an octahydronaphthalene synthon for dihydrocompactin , 1988 .

[88]  J. Ng,et al.  In situ cuprate formation via transmetalation between vinylstannanes and higher order cyanocuprates , 1988 .

[89]  K. Kikukawa,et al.  Reaction of diazonium salts with transition metals: XII. Palladium-catalyzed aryldestannylation of α-styrylstannanes by arenediazonium salts , 1986 .

[90]  J. K. Stille Palladium‐katalysierte Kupplungsreaktionen organischer Elektrophile mit Organozinn‐Verbindungen , 1986 .

[91]  W. Scott,et al.  Palladium-catalyzed coupling of vinyl triflates with organostannanes. Synthetic and mechanistic studies , 1986 .

[92]  D. Milstein,et al.  Palladium-catalyzed coupling of tetraorganotin compounds with aryl and benzyl halides. Synthetic utility and mechanism , 1979 .

[93]  D. Milstein,et al.  A general, selective, and facile method for ketone synthesis from acid chlorides and organotin compounds catalyzed by palladium , 1978 .

[94]  T. Cohen,et al.  Kinetics and mechanism of the copper(I)-induced homogeneous Ullmann coupling of o-bromonitrobenzene , 1976 .

[95]  T. Cohen,et al.  Copper(I)-induced reductive dehalogenation, hydrolysis, or coupling of some aryl and vinyl halides at room temperature , 1975 .