Sonogashira coupling
Named after Kenkichi Sonogashira
Reaction type Coupling reaction
Identifiers
Organic Chemistry Portal sonogashira-coupling
RSC ontology ID RXNO:0000137
Examples and Related Reactions
Similar reactions Copper-free Sonogashira coupling

The Sonogashira reaction is a cross-coupling reaction used in organic synthesis to form carbon–carbon bonds. It employs a palladium catalyst as well as copper co-catalyst to form a carbon–carbon bond between a terminal alkyne and an aryl or vinyl halide.[1]

The Sonogashira Reaction
The Sonogashira Reaction
The Sonogashira reaction
  • R1: aryl or vinyl
  • R2: arbitrary
  • X: I, Br, Cl or OTf

The Sonogashira cross-coupling reaction has been employed in a wide variety of areas, due to its usefulness in the formation of carbon–carbon bonds. The reaction can be carried out under mild conditions, such as at room temperature, in aqueous media, and with a mild base, which has allowed for the use of the Sonogashira cross-coupling reaction in the synthesis of complex molecules. Its applications include pharmaceuticals, natural products, organic materials, and nanomaterials.[1] Specific examples include its use in the synthesis of tazarotene,[2] which is a treatment for psoriasis and acne, and in the preparation of SIB-1508Y, also known as Altinicline,[3] a nicotinic receptor agonist.

History

The alkynylation reaction of aryl halides using aromatic acetylenes was reported in 1975 in three independent contributions by Cassar,[4] Dieck and Heck[5] as well as Sonogashira, Tohda and Hagihara.[6] All of the reactions employ palladium catalysts to afford the same reaction products. However, the protocols of Cassar and Heck are performed solely by the use of palladium and require harsh reaction conditions (i.e. high reaction temperatures). The use of copper-cocatalyst in addition to palladium complexes in Sonogashira's procedure enabled the reactions to be carried under mild reaction conditions in excellent yields. A rapid development of the Pd/Cu systems followed and enabled myriad synthetic applications, while Cassar-Heck conditions were left, maybe unjustly, all but forgotten.[7] The reaction's remarkable utility can be evidenced by the amount of research still being done on understanding and optimizing its synthetic capabilities as well as employing the procedures to prepare various compounds of synthetic, medicinal or material/industrial importance.[7] Among the cross-coupling reactions it follows in the number of publications right after Suzuki and Heck reaction[8] and a search for the term "Sonogashira" in SciFinder provides over 1500 references for journal publications between 2007 and 2010.[7]

The Sonogashira reaction has become so well known that often all reactions that use modern organometallic catalyst to couple alkyne motifs are termed some variant of "Sonogashira reaction", despite the fact that these reactions are not carried out under true Sonogashira reaction conditions.[7]

Mechanism

Catalytic cycle for the Sonogashira reaction[7]

The reaction mechanism is not clearly understood, but the textbook mechanism revolves around a palladium cycle which is in agreement with the "classical" cross-coupling mechanism, and a copper cycle, which is less well known.[9]

The palladium cycle

  • Palladium precatalyst species are activated under reaction conditions to form a reactive Pd0 compound, A. The exact identity of the catalytic species depends strongly upon reaction conditions. With simple phosphines, such as PPh3 (n=2), and in case of bulky phosphines (i.e., P(o-Tol)
    3    ) it was demonstrated that monoligated species (n=1) are formed.[10] Furthermore, some results point to the formation of anionic palladium species, [L2Pd0Cl]− , which could be the real catalysts in the presence of anions and halides.[11]
  • The active Pd0 catalyst is involved in the oxidative addition step with the aryl or vinyl halide substrate to produce PdII species B. Similar to the above discussion, its structure depends on the employed ligands. This step is believed to be the rate-limiting step of the reaction.
  • Complex B reacts with copper acetylide, complex F, in a transmetallation step, yielding complex C and regenerating the copper catalyst.
  • The structure of complex C depends on the properties of the ligands. For the facile reductive elimination to occur, the substrate motifs need to be in close vicinity, i.e. cis-orientation, so there can be trans-cis isomerisation involved. In reductive elimination the product tolane is expelled from the complex and the active Pd catalytic species is regenerated.

The copper cycle

  • The copper cycle is not entirely well described. It is suggested that the presence of a base results in the formation of a π-alkyne complex E. This increases the acidity of the terminal proton and leads to the formation of copper acetylide, complex F, upon deprotonation.
  • Acetylide F is then involved in the transmetallation reaction with palladium intermediate B.

The mechanism of a copper-free Sonogashira variant

Although beneficial for the effectiveness of the reaction, the use of copper salts in "classical" Sonogashira reaction is accompanied with several drawbacks, such as the application of environmentally unfriendly reagents, the formation of undesirable alkyne homocoupling (Glaser side products), and the necessity of strict oxygen exclusion in the reaction mixture. Thus, with the aim of excluding copper from the reaction, a lot of effort was undertaken in the developments of Cu-free Sonogashira reaction. Along the development of new reaction conditions, many experimental and computational studies focused on elucidation of reaction mechanism.[12] Until recently, the exact mechanism by which the Cu-free reaction occurs was under debate, with critical mechanistic questions unanswered.[7] It was shown in 2018 by Košmrlj et al. that the reaction proceeds along the two interconnected Pd0/PdII catalytic cycles.[13][14]

Mechanism for the Cu-free Sonogashira reaction.
Mechanism for the Cu-free Sonogashira reaction.[13][14]
Mechanism for the Cu-free Sonogashira reaction.[13][14]
  • Similar to the original mechanism, the Pd0 cycle begins with the oxidative addition of the aryl halide or triflate to the Pd0 catalyst, forming complex B and activating aryl halide substrate for the reaction.
  • Acetylene is activated in the second, PdII mediated cycle. Phenylacetylene was proven to form Pd monoacetylide complex D as well as Pd bisacetylide complex F under mild reaction conditions.
  • Both activated species, namely complexes B and F, are involved in the transmetallation step, forming complex C and regenerating D.
  • The resulting products of reductive elimination, disubstituted alkyne product as well as regenerated Pd0 catalytic species, complete the Pd0 catalytic cycle.

It was demonstrated that amines are competitive to the phosphines and can also participate as ligands L in the described reaction species. Depending on the rate of the competition between amine and phosphines, a dynamic and complex interplay is expected when using different coordinative bases.[15][16][13][14]

Reaction conditions

The Sonogashira reaction is typically run under mild conditions.[17] The cross-coupling is carried out at room temperature with a base, typically an amine, such as diethylamine,[6] that also acts as the solvent. The reaction medium must be basic to neutralize the hydrogen halide produced as the byproduct of this coupling reaction, so alkylamine compounds such as triethylamine and diethylamine are sometimes used as solvents, but also DMF or ether can be used as solvent. Other bases such as potassium carbonate or cesium carbonate are occasionally used. In addition, deaerated conditions are formally needed for Sonogashira coupling reactions because the palladium(0) complexes are unstable in the air, and oxygen promotes the formation of homocoupled acetylenes. Recently, development of air-stable organopalladium catalysts enable this reaction to be conducted in the ambient atmosphere. In addition, R.M Al-Zoubi and co-workers successfully developed a method with high regioselectivity for 1,2,3-trihaloarene derivatives in good to high yields under ambient conditions.[18]

Catalysts

Typically, two catalysts are needed for this reaction: a zerovalent palladium complex and a copper(I) halide salt. Common examples of palladium catalysts include those containing phosphine ligands such as [Pd(PPh3)4]. Another commonly used palladium source is [[Bis(triphenylphosphine)palladium chloride|[Pd(PPh3)2Cl2]]], but complexes containing bidentate phosphine ligands, such as [Pd(dppe)Cl2], [Pd(dppp)Cl2], and [Pd(dppf)Cl2] have also been used.[9] The drawback to such catalysts is the need for high loadings of palladium (up to 5 mol %), along with a larger amount of a copper co-catalyst.[9] PdII complexes are in fact pre-catalysts since they must be reduced to Pd0 before catalysis can begin. PdII complexes generally exhibit greater stability than Pd0 complexes and can be stored under normal laboratory conditions for months.[19] PdII catalysts are reduced to Pd0 in the reaction mixture by an amine, a phosphine ligand, or another reactant in the mixture allowing the reaction to proceed.[20] For instance, oxidation of triphenylphosphine to triphenylphosphine oxide can lead to the formation of Pd0 in situ when [Pd(PPh3)2Cl2] is used.

Copper(I) salts, such as CuI, react with the terminal alkyne and produce a copper(I) acetylide, which acts as an activated species for the coupling reactions. Cu(I) is a co-catalyst in the reaction, and is used to increase the rate of the reaction.[7]

Aryl halides and pseudohalides

The choice of aryl halide or pseudohalide substrate (sp2-carbon) is one of the factors that mainly influence the reactivity of the Sonogashira catalytic system. The reactivity of halides is higher towards iodine, and vinyl halides are more reactive than analogous aryl halides. The coupling of aryl iodides proceeds at room temperature, while aryl bromides require heating.

The rate of reaction of sp2 carbons. Vinyl iodide > vinyl triflate > vinyl bromide > vinyl chloride > aryl iodide > aryl triflate > aryl bromide >>> aryl chloride.[9]

This difference in reactivity can be exploited to selectively couple an aryl iodide but not an aryl bromide, by performing the reaction at room temperature.[9] An example is the symmetrical Sonogashira coupling of two equivalents of 1-bromo-4-iodobenzene with trimethylsilylacetylene (with the trimethylsilyl group removed in situ) to form bis(4-bromophenyl)acetylene.[21]

Symmetrical Sonogashira coupling of 1-bromo-4-iodobenzene with trimethylsilylacetylene with in situ TMSA deprotection to form bis(4-bromophenyl)acetylene.[21]

Aryl triflates can also be employed instead of aryl halides.

Arenediazonium precursors

Arenediazonium salts have been reported as an alternative to aryl halides for the Sonogashira coupling reaction. Gold(I) chloride has been used as co-catalyst combined with palladium(II) chloride in the coupling of arenediazonium salts with terminal alkynes, a process carried out in the presence of bis-2,6-diisopropylphenyl dihydroimidazolium chloride (IPr NHC) (5 mol%) to in situ generate a NHC–palladium complex, and 2,6-di-tert-butyl-4-methylpyridine (DBMP) as base in acetonitrile as solvent at room temperature.[22] This coupling can be carried out starting from anilines by formation of the diazonium salt followed by in situ Sonogashira coupling, where anilines are transformed into diazonium salt and furtherly converted into alkyne by coupling with phenylacetylene.

Alkynes

Various aromatic alkynes can be employed to yield desired disubstituted products with satisfactory yields. Aliphatic alkynes are generally less reactive.

Bases

Due to the crucial role of base, specific amines must be added in excess or as solvent for the reaction to proceed. It has been discovered that secondary amines such as piperidine, morpholine, or diisopropylamine in particular can react efficiently and reversibly with trans–RPdX(PPh3)2 complexes by substituting one PPh3 ligand. The equilibrium constant of this reaction is dependent on R, X, a factor for basicity, and the amine's steric hindrance.[23] The result is competition between the amine and the alkyne group for this ligand exchange, which is why the amine is generally added in excess to promote preferential substitution.

Protecting groups

Trimethylsilylacetylene is a commonly used reagent in Sonogashira couplings.[24] Being a liquid it is a more convenient reagent than the gaseous acetylene, and the trimethylsilyl group prevents addition onto the other end of the acetylene group. The trimethylsilyl group can then be removed using TBAF, yielding a monosubstituted acetylene. It may also be removed using DBU in situ, allowing the monosubstituted acetylene to react further with another aryl halide to form diphenylacetylene and derivatives.[21]

Reaction variations

Copper-free Sonogashira coupling

While a copper co-catalyst is added to the reaction to increase reactivity, the presence of copper can result in the formation of alkyne dimers. This leads to what is known as the Glaser coupling reaction, which is an undesired formation of homocoupling products of acetylene derivatives upon oxidation. As a result, when running a Sonogashira reaction with a copper co-catalyst, it is necessary to run the reaction in an inert atmosphere to avoid the unwanted dimerization. Copper-free variations to the Sonogashira reaction have been developed to avoid the formation of the homocoupling products.[19][25] There are other cases when the use of copper should be avoided, such as coupling reactions involving substrates which potential copper ligands, for instance free-base porphyrins.[9]

Inverse Sonogashira coupling

In an inverse Sonogashira coupling the reactants are an aryl or vinyl compound and an alkynyl halide.[26]

Catalyst variations

Silver co-catalysis

In some cases stoichiometric amounts of silver oxide can be used in place of CuI for copper-free Sonogashira couplings.[9]

Nickel catalysts

Recently, a nickel-catalyzed Sonogashira coupling has been developed which allows for the coupling of non-activated alkyl halides to acetylene without the use of palladium, although a copper co-catalyst is still needed.[27] It has also been reported that gold can be used as a heterogeneous catalyst, which was demonstrated in the coupling of phenylacetylene and iodobenzene with an Au/CeO2 catalyst.[28][29] In this case, catalysis occurs heterogeneously on the Au nanoparticles,[29][30] with Au(0) as the active site.[31] Selectivity to the desirable cross coupling product was also found to be enhanced by supports such as CeO2 and La2O3.[31] Additionally, iron-catalyzed Sonogashira couplings have been investigated as relatively cheap and non-toxic alternatives to palladium. Here, FeCl3 is proposed to act as the transition-metal catalyst and Cs2CO3 as the base, thus theoretically proceeding through a palladium-free and copper-free mechanism.[32]

Palladium-free Sonogashira reaction catalysed by iron
Palladium-free Sonogashira reaction catalysed by iron
Palladium-free Sonogashira reaction catalysed by iron[32]

While the copper-free mechanism has been shown to be viable, attempts to incorporate the various transition metals mentioned above as less expensive alternatives to palladium catalysts have shown a poor track record of success due to contamination of the reagents with trace amounts of palladium, suggesting that these theorized pathways are extremely unlikely, if not impossible, to achieve.[33]

Studies have shown that organic and inorganic starting materials can also contain enough (ppb level) palladium for the coupling.[34]

Gold and palladium co-catalysis

A highly efficient gold and palladium combined methodology for the Sonogashira coupling of a wide array of electronically and structurally diverse aryl and heteroaryl halides has been reported.[35] The orthogonal reactivity of the two metals shows high selectivity and extreme functional group tolerance in Sonogashira coupling. A brief mechanistic study reveals that the gold-acetylide intermediate enters into palladium catalytic cycle at the transmetalation step.

Dendrimeric palladium complexes

The issues dealing with recovery of the often expensive catalyst after product formation poses a serious drawback for large-scale applications of homogeneous catalysis.[9] Structures known as metallodendrimers combine the advantages of homogeneous and heterogeneous catalysts, as they are soluble and well defined on the molecular level, and yet they can be recovered by precipitation, ultrafiltration, or ultracentrifugation.[36] Some recent examples can be found about the use of dendritic palladium complex catalysts for the copper-free Sonogashira reaction. Thus, several generations of bidentate phosphine palladium(II) polyamino dendritic catalysts have been used solubilized in triethylamine for the coupling of aryl iodides and bromides at 25-120 °C, and of aryl chlorides, but in very low yields.[37]

A recyclable polymeric phosphine ligand[38]

The dendrimeric catalysts could usually be recovered by simple precipitation and filtration and reused up to five times, with diminished activity produced by dendrimer decomposition and not by palladium leaching being observed. These dendrimeric catalysts showed a negative dendritic effect; that is, the catalyst efficiency decreases as the dendrimer generation increases. A recyclable polymeric phosphine ligand is obtained from ring-opening metathesis polymerization of a norbornene derivative, and has been used in the copper co-catalyzed Sonogashira reaction of methyl p-iodobenzoate and phenylacetylene using Pd(dba)2·CHCl3 as a palladium source.[38] Despite recovery by filtration, polymer catalytic activity decreased by approximately 4-8% in each recycle experiment.

Nitrogen ligands

Pyridines and pyrimidines have shown good complexation properties for palladium and have been employed in the formation of catalysts suitable for Sonogashira couplings. The dipyrimidyl-palladium complex shown below has been employed in the copper-free coupling of iodo-, bromo-, and chlorobenzene with phenylacetylene using N-butylamine as base in THF solvent at 65 °C. Furthermore, all structural features of this complex have been characterized by extensive X-ray analysis, verifying the observed reactivity.[39]

More recently, the dipyridylpalladium complex has been obtained and has been used in the copper-free Sonogashira coupling reaction of aryl iodides and bromides in N-methylpyrrolidinone (NMP) using tetra-n-butylammonium acetate (TBAA) as base at room temperature. This complex has also been used for the coupling of aryl iodides and bromides in refluxing water as solvent and in the presence of air, using pyrrolidine as base and TBAB as additive,[40] although its efficiency was higher in N-methylpyrrolidinone (NMP) as solvent.

Coupling of a diiodo substrate catalysed by the dipyridylpalladium complex.[41]

N-heterocyclic carbene (NHC) palladium complexes

N-heterocyclic carbenes (NHCs) have become one of the most important ligands in transition-metal catalysis. The success of normal NHCs is greatly attributed to their superior σ-donating capabilities as compared to phosphines, which is even greater in abnormal NHC counterparts. Employed as ligands in palladium complexes, NHCs contributed greatly to the stabilization and activation of precatalysts and have therefore found application in many areas of organometallic homogeneous catalysis, including Sonogashira couplings.[9][42][43]

An example of palladium(II) derived complex with N-heterocyclic ligand
An example of palladium(II) derived complex with N-heterocyclic ligand
An example of cationic PdNHC complex for efficient catalysis of Sonogashira reaction in water.
An example of cationic PdNHC complex for efficient catalysis of Sonogashira reaction in water.
An example of palladium(II) derived complex with normal NHC ligand.[44] Efficient iPEPPSI catalyst for Cu-free Sonogashira reaction in water.[42]

Interesting examples of abnormal NHCs are based on the mesoionic 1,2,3-triazol-5-ylidene structure. An efficient, cationic palladium catalyst of PEPPSI type, i.e., iPEPPSI (internal pyridine-enhanced precatalyst preparation stabilization and initiation) was demonstrated to efficiently catalyse the copper-free Sonogashira reaction in water as the only solvent, under aerobic conditions, in the absence of copper, amines, phosphines and other additives.[42]

Metal oxide catalysts

Recent developments in heterogeneous catalysis enabled the use of metal oxide materials such as cuprous oxide nanocatalysts in flow processing technologies, which can enable the economical production of active pharmaceutical ingredients and various other fine chemicals.[45]

Applications in synthesis

Sonogashira couplings are employed in a wide array of synthetic reactions, primarily due to their success in facilitating the following challenging transformations:

Alkynylation reactions

The coupling of a terminal alkyne and an aromatic ring is the pivotal reaction when talking about applications of the copper-promoted or copper-free Sonogashira reaction. The list of cases where the typical Sonogashira reaction using aryl halides has been employed is large, and choosing illustrative examples is difficult. A recent use of this methodology is shown below for the coupling of iodinated phenylalanine with a terminal alkyne derived from d-biotin using an in situ generated Pd0 species as catalyst, which allowed the preparation of alkyne-linked phenylalanine derivative for bioanalytical applications.[46] There are also examples of the coupling partners both being attached to allyl resins, with the Pd0 catalyst effecting cleavage of the substrates and subsequent Sonogashira coupling in solution.[47]

Alkynylation of phenylalanine.[46]

Natural products

Many metabolites found in nature contain alkyne or enyne moieties, and therefore, the Sonogashira reaction has found frequent utility in their syntheses.[48] Several of the most recent and promising applications of this coupling methodology toward the total synthesis of natural products exclusively employed the typical copper-cocatalyzed reaction.

An example of the coupling of an aryl iodide to an aryl acetylene can be seen in the reaction of an iodinated alcohol and tris(isopropyl)silylacetylene, which gave an alkyne, an intermediate in the total synthesis of the benzindenoazepine alkaloid bulgaramine.[49]

Sonogashira reaction in the total synthesis of bulgaramine.[49]


There are other recent examples of the use of aryl iodides for the preparation of intermediates under typical Sonogashira conditions, which, after cyclization, yield natural products such as benzylisoquinoline [50] or indole alkaloids[51] An example is the synthesis of the benzylisoquinoline alkaloids (+)-(S)-laudanosine and (–)-(S)-xylopinine. The synthesis of these natural products involved the use of Sonogashira cross-coupling to build the carbon backbone of each molecule.[50]

Natural products (+)-(S)-laudanosine and (–)-(S)-xylopinine synthesized using the Sonogashira cross-coupling reaction.[50]

Enynes and enediynes

The 1,3-enyne moiety is an important structural unit for biologically active and natural compounds. It can be derived from vinylic systems and terminal acetylenes by using a configuration-retention stereospecific procedure such as the Sonogashira reaction. Vinyl iodides are the most reactive vinyl halides to Pd0 oxidative addition, and their use is therefore most frequent for Sonogashira cross-coupling reactions due to the usually milder conditions employed. Some examples include:

  • The coupling of 2-iodoprop-2-en-1-ol with a wide range of acetylenes.[52]
  • The preparation of alk-2-ynylbuta-1,3-dienes from the cross-coupling of a diiodide and phenylacetylene, as shown below.[53]
Synthesis of an alk-2-ynylbuta-1,3-diene accomplished by Sonogashira coupling.[53]

Pharmaceuticals

The versatility of the Sonogashira reaction makes it a widely used reaction in the synthesis of a variety of compounds. One such pharmaceutical application is in the synthesis of SIB-1508Y, which is more commonly known as Altinicline. Altinicline is a nicotinic acetylcholine receptor agonist that has shown potential in the treatment of Parkinson's disease, Alzheimer's disease, Tourette's syndrome, schizophrenia, and attention deficit hyperactivity disorder (ADHD).[3][54] As of 2008, Altinicline has undergone Phase II clinical trials.[55][56]

Use of the Sonogashira cross-coupling reaction in the synthesis of SIB-1508Y.[3]

The Sonogashira cross coupling reaction can be used in the synthesis of imidazopyridine derivatives.[57]

Synthesis of imidazopyridine derivatives.[57]

References

  1. 1 2 Sonogashira, K. (2002), "Development of Pd-Cu catalyzed cross-coupling of terminal acetylenes with sp2-carbon halides", J. Organomet. Chem., 653 (1–2): 46–49, doi:10.1016/s0022-328x(02)01158-0
  2. ↑ King, A.O.; Yasuda, N. (2005), "A Practical and Efficient Process for the Preparation of Tazarotene", Org. Process Res. Dev., 9 (5): 646–650, doi:10.1021/op050080x
  3. 1 2 3 King, A. O.; Yasuda, N. (2004), Palladium-Catalyzed Cross-Coupling Reactions in the Synthesis of Pharmaceuticals Organometallics in Process Chemistry, Top. Organomet. Chem., vol. 6, pp. 205–245, doi:10.1007/b94551, ISBN 978-3-540-01603-8
  4. ↑ Cassar, L. (1975), "Synthesis of aryl- and vinyl-substituted acetylene derivatives by the use of nickel and palladium complexes", J. Organomet. Chem., 93 (2): 253–257, doi:10.1016/S0022-328X(00)94048-8
  5. ↑ Dieck, H.A.; Heck, R.F. (1975), "Palladium catalyzed synthesis of aryl, heterocyclic and vinylic acetylene derivatives", J. Organomet. Chem., 93 (2): 259–263, doi:10.1016/S0022-328X(00)94049-X
  6. 1 2 Sonogashira, K.; Tohda, Y.; Hagihara, N. (1975), "A convenient synthesis of acetylenes: catalytic substitutions of acetylenic hydrogen with bromoalkenes, iodoarenes and bromopyridines", Tetrahedron Lett., 16 (50): 4467–4470, doi:10.1016/s0040-4039(00)91094-3
  7. 1 2 3 4 5 6 7 Chinchilla, R.; Nájera, C. (2011), "Recent advances in Sonogashira reactions", Chem. Soc. Rev., 40 (10): 5084–5121, doi:10.1039/c1cs15071e, PMID 21655588
  8. ↑ Seechurn, C. C. C.; Kitching, M. O.; Colacot, T. J.; Snieckus, V. (2012), "Palladium-Catalyzed Cross-Coupling: A Historical Contextual Perspective to the 2010 Nobel Prize", Angew. Chem. Int. Ed., 51 (21): 5062–5085, doi:10.1002/anie.201107017, PMID 22573393
  9. 1 2 3 4 5 6 7 8 9 Chinchilla, R.; Nájera, C. (2007), "The Sonogashira Reaction: A Booming Methodology in Synthetic Organic Chemistry", Chem. Rev., 107 (3): 874–922, doi:10.1021/cr050992x, PMID 17305399
  10. ↑ Stambuli, J. P.; Buhl, M.; Hartwig, J. F. (2002), "Synthesis, Characterization, and Reactivity of Monomeric, Arylpalladium Halide Complexes with a Hindered Phosphine as the Only Dative Ligand", J. Am. Chem. Soc., 124 (32): 9346–9347, doi:10.1021/ja0264394, PMID 12167009
  11. ↑ Amatore, C.; Jutand, A. (2000), "Anionic Pd0 and PdII Intermediates in Palladium-Catalyzed Heck and Cross-Coupling Reactions", Acc. Chem. Res., 33 (5): 314–321, CiteSeerX 10.1.1.612.7347, doi:10.1021/ar980063a, PMID 10813876
  12. ↑ Soheili, A.; Albaneze-Walker, J.; Murry, J. A.; Dormer, P. G.; Hughes, D. L. (2003), "Efficient and General Protocol for the Copper-Free Sonogashira Coupling of Aryl Bromides at Room Temp", Org. Lett., 5 (22): 4191–4194, doi:10.1021/ol035632f, PMID 14572282
  13. 1 2 3 4 Gazvoda, M.; Virant, M.; Pinter, B.; Košmrlj, J. (2018). "Mechanism of copper-free Sonogashira reaction operates through palladium-palladium transmetallation". Nat. Commun. 9 (1): 4814. Bibcode:2018NatCo...9.4814G. doi:10.1038/s41467-018-07081-5. PMC 6240041. PMID 30446654.
  14. 1 2 3 4 Virant, Miha (2019). Development of homogeneous palladium catalytic systems for selected transformations of terminal acetylenes (PhD). University of Ljubljana.
  15. ↑ Tougerti, A.; Negri, S.; Jutand, A. (2007), "Mechanism of the Copper-Free Palladium-Catalyzed Sonogashira Reactions: Multiple Role of Amines", Chem. Eur. J., 13 (2): 666–676, doi:10.1002/chem.200600574, PMID 16991183
  16. ↑ Plenio, H. (2008), "Catalysts for the Sonogashira Coupling—The Crownless Again Shall Be King", Angew. Chem. Int. Ed., 47 (37): 6954–6956, doi:10.1002/anie.200802270, PMID 18683173
  17. ↑ Kohnen, A. L; Danheiser, R. L.; Denmark S. E.; Liu X. (2007), "Synthesis of Terminal 1,3-Diynes Via Sonogashira Coupling of Vinylidene Chloride Followed by Elimination. Preparation of 1,3-Decadiyne", Org. Synth., 84: 77–87, doi:10.15227/orgsyn.084.0077, PMC 2901882, PMID 20628544
  18. ↑ Al-Zoubi, Raed (16 April 2020). "Palladium-catalyzed highly regioselective mono and double Sonogashira cross-coupling reactions of 5-substituted-1,2,3-triiodobenzene under ambient conditions†". RSC Adv. 10 (28): 16376. Bibcode:2020RSCAd..1016366A. doi:10.1039/d0ra01569e. PMC 9053030.
  19. 1 2 Bohm, V. P. W.; Herrmann, W. A. (2000), "A Copper-Free Procedure for the Palladium-Catalyzed Sonogashira Reaction of Aryl Bromides with Terminal Alkynes at Room Temperature", Eur. J. Org. Chem., 200 (22): 3679–3681, doi:10.1002/1099-0690(200011)2000:22<3679::aid-ejoc3679>3.0.co;2-x
  20. ↑ Yin, L.; Liebscher, J. (2006), "Carbon-Carbon Coupling Reactions Catalyzed by Heterogeneous Palladium Catalysts", Chem. Rev., 107 (1): 133–173, doi:10.1021/cr0505674, PMID 17212474
  21. 1 2 3 Mio, Matthew J.; Kopel, Lucas C.; Braun, Julia B.; Gadzikwa, Tendai L.; Hull, Kami L.; Brisbois, Ronald G.; Markworth, Christopher J.; Grieco, Paul A. (2002). "One-Pot Synthesis of Symmetrical and Unsymmetrical Bisarylethynes by a Modification of the Sonogashira Coupling Reaction". Organic Letters. 4 (19): 3199–3202. doi:10.1021/ol026266n.
  22. ↑ Panda B., Sarkar T. K. (2010). "Gold and palladium combined for the Sonogashira-type cross-coupling of arenediazonium salts". Chem. Commun. 46 (18): 3131–3133. doi:10.1039/c001277g. PMID 20361097.
  23. ↑ Jutand, A.; Négri, S.; Principaud; A. (2005), "Formation of ArPdXL(amine) Complexes by Substitution of One Phosphane Ligand by an Amine in trans-ArPdX(PPh3)2 Complexes", Eur. J. Inorg. Chem., 2005 (4): 631–635, doi:10.1002/ejic.200400413
  24. ↑ Godson C. Nwokogu; Saskia Zemolka; Florian Dehme (2007). "Trimethylsilylacetylene". EROS. doi:10.1002/047084289X.rt288.pub2. ISBN 978-0-471-93623-7.
  25. ↑ Mery, D.; Heuze, K.; Astruc, D. (2003), "A very efficient, copper-free palladium catalyst for the Sonogashira reaction with aryl halides", Chem. Commun., 15 (15): 1934–1935, doi:10.1039/B305391C, PMID 12932040
  26. ↑ Dudnik, A.; Gevorgyan, V. (2010). "Formal Inverse Sonogashira Reaction: Direct Alkynylation of Arenes and Heterocycles with Alkynyl Halides". Angew. Chem. Int. Ed. 49 (12): 2096–2098. doi:10.1002/anie.200906755. PMC 3132814. PMID 20191647.
  27. ↑ Vechorkin, O.; Barmaz, D.; Proust, V.; Hu, X. (2009), "Ni-Catalyzed Sonogashira Coupling of Nonactivated Alkyl Halides: Orthogonal Functionalization of Alkyl Iodides, Bromides, and Chlorides", J. Am. Chem. Soc., 131 (34): 12078–12079, doi:10.1021/ja906040t, PMID 19670863
  28. ↑ Gonzalez-Arallano, C.; Abad, A.; Corma, A.; Garcia, H.; Iglesias, M.; Sanchez, F. (2007), "Catalysis by Gold(I) and Gold(III): A Parallelism between Homo- and Heterogeneous Catalysts for Copper-Free Sonogashira Cross-Coupling Reactions", Angew. Chem. Int. Ed., 46 (9): 1536–1538, doi:10.1002/anie.200604746, PMID 17226890
  29. 1 2 Corma, A.; Juarez, R.; Boronat, M.; Sanchez, F.; Iglesias, M.; Garcia, H. (2011), "Gold catalyzes the Sonogashira coupling reaction without the requirement of palladium impurities", Chem. Commun., 47 (5): 1446–1448, doi:10.1039/C0CC04564K, PMID 21183985
  30. ↑ Kyriakou, G.; Beaumont, S. K.; Humphrey, S. M.; Antonetti, C.; Lambert, R. M. (2010), "Sonogashira Coupling Catalyzed by Gold Nanoparticles: Does Homogeneous or Heterogeneous Catalysis Dominate?", ChemCatChem, 2 (11): 1444–1449, doi:10.1002/cctc.201000154, S2CID 96700925
  31. 1 2 Beaumont, S. K.; Kyriakou, G.; Lambert, R. M. (2010), "Identity of the active site in gold nanoparticle-catalyzed Sonogashira coupling of phenylacetylene and iodobenzene." (PDF), J. Am. Chem. Soc., 132 (35): 12246–12248, doi:10.1021/ja1063179, PMID 20715838
  32. 1 2 M. Carril; A. Correa; C. Bolm (2008), "Iron-Catalyzed Sonogashira Reaction", Angew. Chem., 120 (26): 4940–4943, Bibcode:2008AngCh.120.4940C, doi:10.1002/ange.200801539
  33. ↑ Thorsten Lauterbach; Madeleine Livendahl; Antonio Rosellon; Pablo Espinet; Antonio M. Echavarren (2010), "Unlikeliness of Pd-Free Gold(I)-Catalyzed Sonogashira Coupling Reactions", Org. Lett., 12 (13): 3006–3009, doi:10.1021/ol101012n, PMID 20515017
  34. ↑ Tolnai, L. G.; Gonda, ZS.; Novák, Z. (2010). "Dramatic Impact of ppb Levels of Palladium on the "Copper-Catalyzed" Sonogashira Coupling". Chem. Eur. J. 16 (39): 11822–11826. doi:10.1002/chem.201001880. PMID 20821769.
  35. ↑ Panda, B.; Sarkar, T. K. (2013), "Gold and Palladium Combined for the Sonogashira Coupling of Aryl and Heteroaryl Halides", Synthesis, 45 (6): 817–829, doi:10.1055/s-0032-1318119
  36. ↑ Astruc, Didier; Heuzé, Karine; Gatard, Sylvain; Méry, Denise; Nlate, Sylvain; Plault, Lauriane (February 2005). "Metallodendritic Catalysis for Redox and Carbon—Carbon Bond Formation Reactions: A Step towards Green Chemistry". Adv. Synth. Catal. 347 (2–3): 329–338. doi:10.1002/adsc.200404247.
  37. ↑ Heuzé, Karine; Méry, Denise; Gauss, Dominik; Astruc, Didier (2003). "Copper-free, recoverable dendritic Pd catalysts for the Sonogashira reaction". Chem. Commun. (18): 2274–2275. doi:10.1039/B307116M. PMID 14518871.
  38. 1 2 Yang, Yun-Chin; Luh, Tien-Yau (December 2003). "Polymeric Phosphine Ligand from Ring-Opening Metathesis Polymerization of a Norbornene Derivative. Applications in the Heck, Sonogashira, and Negishi Reactions" (PDF). J. Org. Chem. 68 (25): 9870–9873. doi:10.1021/jo035318z. PMID 14656129.
  39. ↑ Buchmeiser, Michael R.; Schareina, Thomas; Kempe, Rhett; Wurst, Klaus (2001). "Bis(pyrimidine)-based palladium catalysts: Synthesis, X-ray structure and applications in Heck–, Suzuki–, Sonogashira–Hagihara couplings and amination reactions". J. Organomet. Chem. 634: 39–46. doi:10.1016/S0022-328X(01)01083-X.
  40. ↑ Gil-Moltó, J.; Karström, S.; Nájera, C. (2005), "Di(2-pyridyl)methylamine–palladium dichloride complex covalently anchored to a styrene-maleic anhydride co-polymer as recoverable catalyst for C–C cross-coupling reactions in water", Tetrahedron, 61 (51): 12168–12176, doi:10.1016/j.tet.2005.08.122
  41. ↑ Gil-Moltó, J.; Nájera, C. (2005), "Palladium(II) Chloride and a (Dipyridin-2-ylmethyl)amine-DerivedPalladium(II) Chloride Complex as Highly Efficient Catalysts for the Synthesisof Alkynes in Water or in NMP and of Diynes in the Absence of Reoxidant", Eur. J. Org. Chem., 2005 (19): 4073–4081, doi:10.1002/ejoc.200500319
  42. 1 2 3 Gazvoda, M.; Virant, M; Pevec, A.; Urankar, D.; Bolje, A.; Kočevar, M.; Košmrlj, J. (2016), "A mesoionic bis(Py-tzNHC) palladium(II) complex catalyses green Sonogashira reaction through an unprecedented mechanism", Chem. Commun., 52 (8): 1571–1574, doi:10.1039/c5cc08717a, PMID 26575368
  43. ↑ Crudden, Cathleen M.; Allen, Daryl P. (December 2004). "Stability and reactivity of N-heterocyclic carbene complexes". Coord. Chem. Rev. 248 (21–24): 2247–2273. doi:10.1016/j.ccr.2004.05.013.
  44. ↑ Batey, R. A.; Shen, M.; Lough, A. J. (2002), "Carbamoyl-Substituted N-Heterocyclic Carbene Complexes of Palladium(II): Application to Sonogashira Cross-Coupling Reactions", Org. Lett., 4 (9): 1411–1414, doi:10.1021/ol017245g, PMID 11975591
  45. ↑ Ravi Teja Addanki Tirumala.; Andishaeh P. Dadgar.; Farshid Mohammadparast.; Sundaram Bhardwaj Ramakrishnan.; Tong Mou.; Bin Wang.; Marimuthu Andiappan. (2019), "Homogeneous versus heterogeneous catalysis in Cu2O-nanoparticle-catalyzed C–C coupling reactions", Green Chemistry, 21: 5284–5290, doi:10.1039/C9GC01930H, PMID 19670863
  46. 1 2 Corona C.; Bryant B.K.; Arterburn J.B. (2006). "Synthesis of a Biotin-Derived Alkyne for Pd-Catalyzed Coupling Reactions". Org. Lett. 8 (9): 1883–1886. doi:10.1021/ol060458r. PMC 2523258. PMID 16623575.
  47. ↑ Tulla-Puche J.; Barany G (2005). "Development of resin-to-resin transfer reactions (RRTR) using Sonogashira chemistry". Tetrahedron. 61 (8): 2195. doi:10.1016/j.tet.2004.12.029.
  48. ↑ Hong, B.-C.; Nimje, R. Y. (2006). "Catalytic C-C Bond Formation in Natural Products Synthesis: Highlights From The Years 2000-2005". Curr. Org. Chem. 10 (17): 2191-2225. doi:10.2174/138527206778742605.
  49. 1 2 Chinchilla, Rafael; Nájera, Carmen (2007). "The Sonogashira Reaction:  A Booming Methodology in Synthetic Organic Chemistry†". Chemical Reviews. 107 (3): 874–922. doi:10.1021/cr050992x.
  50. 1 2 3 Mujahidin, Didin; Doye, Sven (1 July 2005). "Enantioselective Synthesis of (+)-(S)-Laudanosine and (−)-(S)-Xylopinine". Eur. J. Org. Chem. 2005 (13): 2689–2693. doi:10.1002/ejoc.200500095.
  51. ↑ Pedersen, J. M.; Bowman, W. R.; Elsegood, M. R. J.; Fletcher, A. J.; Lovell, P. J (2005). "Synthesis of Ellipticine: A Radical Cascade Protocol to Aryl- and Heteroaryl-Annulated[b]carbazoles". J. Org. Chem. 70 (25): 10615–10618. doi:10.1021/jo0519920. PMID 16323886.
  52. ↑ Thongsornkleeb, C.; Danheiser, R.L. (2005). "The coupling of 2-iodo-prop-2-enol with a wide range of acetylenes such as TMSA to give enynyl alcohol, which can be oxidized to the corresponding R-alkynylated acroleins". J. Org. Chem. 70 (6): 2364–2367. doi:10.1021/jo047869a. PMC 2897060. PMID 15760233.
  53. 1 2 Shao, L.-X.; Shi, M. (2005), "Facile Synthesis of 2-Alkynyl Buta-1,3-dienes via Sonogashira Cross-Coupling Methodology", J. Org. Chem., 70 (21): 8635–8637, doi:10.1021/jo051434l, PMID 16209628
  54. ↑ Bleicher, L.S.; Cosford, N.D.P.; Herbaut, A.; McCallum, J. S.; McDonald, I. A. (1998), "A Practical and Efficient Synthesis of the Selective Neuronal Acetylcholine-Gated Ion Channel Agonist (S)-(−)-5-Ethynyl-3-(1-methyl-2-pyrrolidinyl)pyridine Maleate (SIB-1508Y)", J. Org. Chem., 63 (4): 1109–1118, doi:10.1021/jo971572d
  55. ↑ Wang, David X.; Booth, Heather; Lerner-Marmarosh, Nicole; Osdene, Thomas S.; Abood, Leo G. (1 September 1998). "Structure-activity relationships for nicotine analogs comparing competition for [3H]nicotine binding and psychotropic potency". Drug Dev. Res. 45 (1): 10–16. doi:10.1002/(SICI)1098-2299(199809)45:1<10::AID-DDR2>3.0.CO;2-G.
  56. ↑ Parkinson Study, Group (14 February 2006). "Randomized placebo-controlled study of the nicotinic agonist SIB-1508Y in Parkinson disease". Neurology. 66 (3): 408–410. doi:10.1212/01.wnl.0000196466.99381.5c. PMID 16476941. S2CID 31720763.
  57. 1 2 Bakherad, M.; Nasr-Isfahani, H.; Keivanloo, A.; Doostmohammadi, N. (2008), "Pd–Cu catalyzed heterocyclization during Sonogashira coupling: synthesis of 2-benzylimidazo[1,2-a]pyridine", J. Organomet. Chem., 49 (23): 3819–3822, doi:10.1016/j.tetlet.2008.03.141
This article is issued from Wikipedia. The text is licensed under Creative Commons - Attribution - Sharealike. Additional terms may apply for the media files.