Boronates arylboronates

The Suzuki coupling of arylboronic acids and aryl halides has proven to be a useful method for preparing C-aryl indoles. The indole can be used either as the halide component or as the boronic acid. 6-Bromo and 7-bromoindolc were coupled with arylboronic acids using Pd(PPh3)4[5]. No protection of the indole NH was necessary. 4-Thallated indoles couple with aryl and vinyl boronic acides in the presence of Pd(OAc)j[6]. Stille coupling between an aryl stannane and a haloindole is another option (Entry 5, Table 14.3). 

Chiral boron(III) Lewis acid catalysts have also been used for enantioselective cycloaddition reactions of carbonyl compounds [17]. The chiral acyloxylborane catalysts 9a-9d, which are also efficient catalysts for asymmetric Diels-Alder reactions [17, 18], can also catalyze highly enantioselective cycloaddition reactions of aldehydes with activated dienes. The arylboron catalysts 9b-9c which are air- and moisture-stable have been shown by Yamamoto et al. to induce excellent chiral induction in the cycloaddition reaction between, e.g., benzaldehyde and Danishefsky s dienes such as 2b with up to 95% yield and 97% ee of the cycloaddition product CIS-3b (Scheme 4.9) [17]. 

The conversion of arylboronic acids to the corresponding neopentyl glycol arylboronic esters has several advantages The esters are readily soluble in organic solvents, shelf stable, non-hygroscopic and easily characterized as a single entity.9 Furthermore, boronic esters can be utilized in many of the transformations where arylboronic acids usually are employed, making them an attractive alternative from a practical point of view. 

If 2,6-pyridinedimethanol is condensed with arylboronic acids in non-polar solvents, the tetrameric boron complexes 74 and 75 are formed rapidly (within 15-30 min) in yields of 80 and 93% (Fig. 20). In both cases only the RSRSI SRSR enantiomeric pair with approximate S4-symmetry is obtained, so that the reaction is diastereoselective. 

The optimal reaction conditions were applied with 59d in the addition of various aryl boronic acids and potassium trifluoroborates to several cyclic and acyclic enones (Fig. 8). Arylboronic acids added to cyclic enones in high yields (89-97%) and with good to excellent selectivities (85-98% ee). Under these conditions, the potassium trifluoroborate reagents reacted at faster rates, but with slightly lower selectivities (83-96% ee). The reactions of acyclic enones with aryl boron reagents gave also excellent yields (83-96%). 

Arylboron Formation Investigated in Micro Reactors Organic synthesis 40 [OS 40] Formation of phenyl esters of boronic add... 

Regarding the use of other metals for this transformation, Shirai and co-workers reported that a system constituted by palladium(II) complex [Pd(p-Cl)(r -aUyl)]2 and thioether-imidazolium chloride 19 achieved the arylation of aldehydes with boronic acids [33] and potassium trifluoroborates in good to excellent yields (Scheme 7.5) [34], More recently, Buffard and Itami showed that a NKcod) / IPr-HCl system could catalyse the reaction of arylboronate esters and inactivated aldehydes and ketones (Scheme 7.5) [35]. 

Boro nophenyl) alanine (BPA) is a practical boron compound which is clinically used for the treatment of not only malignant melanoma but also of brain tumors, in neutron capture therapy (Scheme 1-40) [105, 152, 153]. Although (pinacolato)di-boron (82) is an excellent reagent to afford the corresponding boronate in 88% yield, it strongly resists the hydrolysis to arylboronic acids. Alternatively, the 1,3-diphenyl-propanediol ester (85) is more convenient to deprotect the diol moiety by catalytic hydrogenolysis [105]. 

The use of expensive and unstable ZnPli2 in the preparation of chiral di-arylmethanol derivatives, with electronically and sterically similar aryl rings, made this approach less attractive for the enantioselective synthesis. In order to avoid this inconvenience, other alternative preparations of arylzinc reagents were evaluated.As a first choice, Yus et al. proposed the use of arylboronic adds as a viable source of phenyl (Scheme 4.19). Thus, the reaction of various boronic acids with an excess of ZnEt2 at 70 °C gave the corresponding arylzinc intermediates (probably aryl(ethyl)zincs), which were trapped by reaction with dif-... 

Rhodium-catalyzed Heck-type coupling of boronic acids with activated alkenes was carried out in an aqueous emulsion.82 The couplings between arylboronic acids and activated alkenes catalyzed by a water-soluble tm-butyl amphosrhodium complex were found to progress at room temperature to generate Heck-type products with high yields and excellent selectivity. It was necessary to add two equivalents of the... 

Recently, a rhodium-catalyzed tandem cyclization has been reported with an arylboronic ester bearing a pendant Michael-type acceptor olefin and acetylenic65 or olefinic66 derivatives. This transformation proceeds in a water-containing medium as solvent and proton source. This catalyst system is optimized with electron-rich and bulky ligands to stabilize the rhodium intermediate and decrease the protonolysis of boron derivatives in a protic solvent. 

In the course of their successful syntheses of the marine alkaloids nortopsentins A-D, Kawasaki and co-workers were able to prepare selectively boronic acid 103 from 1 -(tert-butyldimethylsilyl)-3,6-dibromoindole (102) and effect Suzuki couplings to give 3-arylindoles 104 in good yields [117]. Complementary to this chemistry is the direct Pd-catalyzed reaction of 102 with arylboronic acids to give 6-aryl-3-bromoindoles 105 [117]. 

The medicinal importance of 2-aryltryptamines led Chu and co-workers to develop an efficient route to these compounds (130) via a Pd-catalyzed cross-coupling of protected 2-bromotryptamines 128 with arylboronic acids 129 [137]. Several Suzuki conditions were explored and only a partial listing of the arylboronic acids is shown here. In addition, boronic acids derived from naphthalene, isoquinoline, and indole were successfully coupled with 128. The C-2 bromination of the protected tryptamines was conveniently performed using pyridinium hydrobromide perbromide (70-100%). 2-Phenyl-5-(and 7-)azaindoles have been prepared via a Suzuki coupling of the corresponding 2-iodoazaindoles [19]. 

The palladium-catalyzed coupling of boronic acids with aryl and alkenyl halides, the Suzuki reaction, is one of the most efficient C-C cross-coupling processes used in reactions on polymeric supports. These coupling reactions requires only gentle heating to 60-80 °C and the boronic acids used are nontoxic and stable towards air and water. The mild reaction conditions have made this reaction a powerful and widely used tool in the organic synthesis. When the Suzuki reaction is transferred to a solid support, the boronic add can be immobilized or used as a liquid reactant Carboni and Carreaux recently reported the preparation of the macroporous support that can be employed to efficiently immobilize and transform functionalized arylboronic adds (Scheme 3.12) [107, 246, 247]. 

There are several different routes to carboxamides. In most of these reactions, a carboxylic acid is converted to a more reactive intermediate, e.g. the acid chloride, which is then allowed to react with an amine. For practical reasons, it is preferable to form the reactive intermediate in situ. Arylboronic acids with electron-withdrawing groups such as (3,4,5-trifluorophenyl)boronic acid act as highly efficient catalysts in the amidation between carboxylic acids and amines. (3-Nitrophenyl)boronic acid and [3,5-bis(trifluoromethyl)phenyl]boronic acid are also effective eimidation catalysts and commercially available. 

A similar approach was taken for the synthesis of 45 by Miyaura. " Shaughnessy and Booth synthesized the water-soluble alkylphosphine 46, and found it to provide very active palladium catalysts for the reaction of aryl bromides or chlorides with boronic acids. The more sterically demanding ligand 47 was shown to promote the reactions of aryl chlorides with better results than 46. Najera and co-workers recently reported on the synthesis of di(2-pyridyl)-methylamine-palladium dichloride complexes 48a and 48b, and their use in the coupling of a variety of electrophiles (aryl bromides or chlorides, allyl chlorides, acetates or carbonates) with alkyl- or arylboronic acids very low catalyst loadings at Palladium-oxime catalysts 8a and 8b) have also been developed. In conjunction with... 

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