Catalytic Action of Azolium Salts. VI. Preparation of Benzoins and Acyloins by Condensation of Aldehydes Catalyzed by Azolium Salts.

Miyashita, Akira; Suzuki, Yumiko; Iwamoto, Kaoru; Higashino, Takeo

doi:10.1248/cpb.42.2633

Cited by 32 publications

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“…Miyashita und Mitarbeiter verwendeten Imidazolium-und Benzimidazoliumionen wie 386 und 387 als Katalysatoren für die Benzoinreaktion, untersuchten aber keine asymmetrische Variante. [436] Schließlich gelang Enders und Mitarbeitern die Entwicklung einer asymmetrischen NHC-katalysierten Benzoinreaktion unter Verwendung chiraler Triazoliumionen wie 379 und 380.…”

Section: Carbene: Lewis-base-katalyse Mit Doppelaktivierungunclassified

Lewis‐Base‐Katalyse in der organischen Synthese

2008

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Das Erbe von Gilbert Newton Lewis (1875–1946) ist im Wörterbuch der chemischen Bindung und Reaktivität allgegenwärtig. Die Bedeutung seines Konzepts der Donor‐Akzeptor‐Bindung kommt in den eponymen Grundbegriffen für Elektronenpaarakzeptoren (Lewis‐Säuren) und ‐donoren (Lewis‐Basen) zum Ausdruck. Lewis erkannte, dass Säuren nicht automatisch Wasserstoff enthalten müssen (Brønsted‐Säuren) und trug so zum Sturz des “modernen Protonenkults” bei. Seine Entdeckung läutete zunächst die Entwicklung von Lewis‐Säuren als Reagentien und Katalysatoren für organische Reaktionen ein, in den letzten Jahren wurde aber offensichtlich, dass für diese Zwecke auch Lewis‐Basen eingesetzt werden können. Bezüglich der Beschleunigung chemischer Reaktionen ergänzen Lewis‐Basen die entsprechenden Lewis‐Säuren nicht nur elektronisch: Tatsächlich können Lewis‐Basen die Elektrophilie wie auch die Nucleophilie der Verbindungen verstärken, an die sie gebunden werden. Diese unterschiedliche Reaktivität resultiert in einer bemerkenswerten Vielfalt Lewis‐Base‐katalysierter Reaktionen.

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Section: Carbene: Lewis-base-katalyse Mit Doppelaktivierungunclassified

Lewis‐Base‐Katalyse in der organischen Synthese

2008

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“…The 1 H-NMR (500 MHz) and 13 C-NMR (126 MHz) spectra were recorded on a JEOL ECA-500 NMR spectrometer. The IR spectra were recorded on a Shimadzu IRPrestige-21 spectrophotometer.…”

Section: Methodsmentioning

confidence: 99%

“…Since the discovery of stable carbenes by Arduengo 3) in 1991, interest in the use of N-heterocyclic carbene-metal complexes have increased, and it has been demonstrated that they are efficient catalysts in important chemical transformations such as Pd-catalyzed coupling reactions, 4) Ru-catalyzed olefin metathesis, 5) and Rh-catalyzed hydrosilylations. [6][7][8] NHCs have also attracted great attention as organocatalysts in several reactions (e.g., benzoin condensation, [9][10][11][12][13][14] Stetter reaction, [15][16][17] transesterification/acylation reactions, 18,19) and nucleophilic substitution reactions). [20][21][22] Recently, our research group as well as other groups have reported the cyanosilylation of aldehydes catalyzed by NHCs.…”

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confidence: 99%

N-Heterocyclic Carbene Ligands in Copper-Catalyzed Addition of Diethylzinc to N-Sulfonylimines

Bakar

Suzuki

Sato

2008

CHEMICAL & PHARMACEUTICAL BULLETIN

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N-Heterocyclic carbenes (NHCs) are strong s-donating species, showing coordination properties similar to those of phosphines.1,2) Initially, the widespread use of catalysts containing carbene ligands was limited due to their relatively difficult preparation. Since the discovery of stable carbenes by Arduengo 3) in 1991, interest in the use of N-heterocyclic carbene-metal complexes have increased, and it has been demonstrated that they are efficient catalysts in important chemical transformations such as Pd-catalyzed coupling reactions, 4) Ru-catalyzed olefin metathesis, 5) and Rh-catalyzed hydrosilylations. [6][7][8] NHCs have also attracted great attention as organocatalysts in several reactions (e.g., benzoin condensation, [9][10][11][12][13][14] Stetter reaction, [15][16][17] transesterification/acylation reactions, 18,19) and nucleophilic substitution reactions). [20][21][22] Recently, our research group as well as other groups have reported the cyanosilylation of aldehydes catalyzed by NHCs. [23][24][25][26] In the course of our studies on the use of NHCs in organic synthesis, we have found that copper-NHC complexes exhibit the ligand acceleration effect (LAE) in the addition of diethylzinc to N-sulfonylimines. The LAE of copper-NHC complexes was first reported in the addition of diethylzinc to cyclohexenone, 27) and later the asymmetric version of these conjugate addition reactions was accomplished by using chiral NHC ligands. 28,29) In this study, we report our results on the addition of diethylzinc to N-sulfonylimines by using catalytic amounts of copper-NHC complexes. Results and DiscussionIn order to examine the catalytic abilities of the copper-NHC complexes, an addition reaction of diethylzinc to N-(benzylidene)-p-methylbenzenesulfonamide (N-sulfonylimine) 1a 30) was carried out in the presence of 5 mol% of imidazolium salt 2a as a ligand source, 5 mol% of CuI, and 5 mol% of t-BuOK in toluene (Table 1). After reacting at room temperature for 1.5 h, the addition product 3a (50%) and the reduction product 4a (28%) were obtained (Table 1, entry 1). The formation of 4a could be due to the transfer of the b-hydrogen of the ethyl functionality to the CϭN bond of the N-sulfonylimine 1a. In the absence of 2a, the reaction afforded the desired product 3a in only 15% yield and afforded 4a as the major product (entry 2). The reaction without CuI at room temperature for 6 h afforded 3a and 4a in 31% and 22% yields, respectively (entry 3). These results indicate that the LAE of NHC is involved in the addition reaction. To increase the yield of 3a and to suppress the byproduct formation, the reaction was carried out at 0°C. It was observed that though the yield of 3a was increased to 65%, byproduct 4a (12%) was still obtained. Further lowering of the reaction temperature to Ϫ5°C led to the exclusive formation of 3a (entry 5).At Ϫ5°C, the addition reactions of diethylzinc to 1a were carried out by using imidazolium and imidazolinium salts 2b-d as ligand precursors, and the addition products 3a were isolated in go...

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“…[2][3][4][5][6] NHCs are now used as ligands for transition metals in many important chemical transformations such as Pd-catalyzed coupling reactions, 7) Ru-catalyzed olefin metathesis, 8) Rh-catalyzed hydrosilylations, [9][10][11] and Cu-catalyzed conjugate addition reactions. [12][13][14] Moreover, NHCs have attracted considerable attention as organocatalysts in several reactions such as benzoin condensation, [15][16][17][18][19][20] Stetter reaction, [21][22][23] transesterification/acylation reactions, 24,25) and nucleophilic substitution reactions. [26][27][28] In our study on the use of NHCs as ligands in organic transformations, we have recently reported the addition of diethylzinc to N-sulfonylarylimines catalyzed by Cu-NHC complexes, 29) where NHCs exhibit a strong ligand acceleration effect (LAE).…”

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confidence: 99%

Rh-N-Heterocyclic Carbene (NHC) Complex-Catalyzed Addition of Phenylboronic Acid to N-Sulfonyl and N-Phosphinoyl Aldimines

Bakar

Suzuki

Sato

2008

CHEMICAL & PHARMACEUTICAL BULLETIN

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973The synthesis, isolation, and characterization of stable Nheterocyclic carbenes (NHCs) first reported by Arduengo et al. 1) in 1991, have attracted attention for the use of NHCs as ancillary ligands for transition metal complexes. Due to their strong s-donating properties, NHCs can form metal complexes that have high stabilities toward heat, moisture, and air, and they have higher catalytic abilities than their phosphine counterparts. [2][3][4][5][6] NHCs are now used as ligands for transition metals in many important chemical transformations such as Pd-catalyzed coupling reactions, 7) Ru-catalyzed olefin metathesis, 8) Rh-catalyzed hydrosilylations, [9][10][11] and Cu-catalyzed conjugate addition reactions. [12][13][14] Moreover, NHCs have attracted considerable attention as organocatalysts in several reactions such as benzoin condensation, [15][16][17][18][19][20] Stetter reaction, [21][22][23] transesterification/acylation reactions, 24,25) and nucleophilic substitution reactions. [26][27][28] In our study on the use of NHCs as ligands in organic transformations, we have recently reported the addition of diethylzinc to N-sulfonylarylimines catalyzed by 29) where NHCs exhibit a strong ligand acceleration effect (LAE). This finding has prompted us to investigate the applicability of a similar methodology to the Rh-NHC complex-catalyzed addition of phenylboronic acid to imines.The addition reaction of organometallic reagents to imines is one of the most efficient procedures for the synthesis of diarylmethylamines, which are important subunits of biologically significant compounds. [30][31][32][33] Despite many studies on the Rh-phosphine complex-catalyzed addition of arylboronic acids to imines, 34,35) there is only one study, i.e., that by Charette and coworkers, in which the Rh-NHC complex is used.36) Here, we report our results on the addition of arylboronic acid to both N-sulfonylarylimines and N-phosphinoylarylimines by using a catalytic amount of Rh-NHC complexes. Results and DiscussionIn the study by Charette and coworkers, the Rh-NHC complex was prepared in situ using the NHC-transfer reagent Ag-NHC and used as a catalyst in the arylation of pmethylphenyl-N-phosphinoylimine with phenylboronic acid. 36) They showed only one reaction example. We examined the catalytic ability of the Rh-NHC complex generated in situ 37) from azolium salts and [RhCl(cod)] 2 for the arylation of imines. The Rh-NHC complex was prepared from [RhCl(cod)] 2 , 1,3-diadamantylimidazolium chloride 2a, and t-BuOK; then, N-sulfonylphenylimine 1a 38) and phenylboronic acid were added to the mixture. The reaction in dioxane at 70°C for 5 h afforded N-sulfonyldiarylmethylamine 3a in 91% yield (Table 1, entry 1). The reaction without 2a in dioxane afforded the desired product 3a in only 62% yield after 10 h at 70°C (entry 2). These results showed and indicated that the NHC ligand accelerated the addition reaction. The reaction in THF afforded 3a in 48% yield, whereas in toluene, the reaction was very sluggish and gave no adducts (Ta...

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Catalytic Action of Azolium Salts. VI. Preparation of Benzoins and Acyloins by Condensation of Aldehydes Catalyzed by Azolium Salts.

Cited by 32 publications

References 0 publications

Lewis‐Base‐Katalyse in der organischen Synthese

Lewis‐Base‐Katalyse in der organischen Synthese

N-Heterocyclic Carbene Ligands in Copper-Catalyzed Addition of Diethylzinc to N-Sulfonylimines

Rh-N-Heterocyclic Carbene (NHC) Complex-Catalyzed Addition of Phenylboronic Acid to N-Sulfonyl and N-Phosphinoyl Aldimines

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