Multicomponent reactions (MCRs): a useful access to the synthesis of benzo-fused γ-lactams

Benzo-fused γ-lactam rings such as isoindolin-2-ones and 2-oxindoles are part of the structure of many pharmaceutically active molecules. They can be often synthesized by means of multicomponent approaches and recent contributions in this field are summarized in this review. Clear advantages of these methods include the efficiency in saving raw materials and working time. However, there is still a need of new catalytic systems to allow the enantioselective preparation of these heterocycles by multicomponent reactions.


Introduction
Pyrrolidin-2-ones (I, Figure 1) are heterocycles that contain a γ-lactam ring that can be found in many biologically active compounds with natural or synthetic origin [1]. When an aryl group is fused to the 3-and 4-positions of the five-membered heterocycle, isoindolinones (II, Figure 1) are generated, while if such fusion takes place between the 4-and 5-positions of the γ-lactam ring, 2-oxindoles (also named as indolin-2-ones III, Figure 1) are formed.
The isoindolinone structural motif is a part of the core of many natural products [2]. To cite some examples, cichorine [3] and zinnimidine [4] (Figure 2) are simple isoindolinone alkaloids, for which total syntheses have been reported [5], and nuevamine ( Figure 2) is an isoindoloisoquinoline alkaloid [6,7]. Moreover, in this last decade, new compounds such as impatien A [8] (Figure 2) or daldinans B and C [9] have been discovered. Similarly, the 2-oxindole framework is prevalent in a wide range of natural products [10]. For example, convolutamydines [11] are alkaloids containing a dibromohydroxyoxindole moiety, isolated from the Floridian bryozoan Amathia convulata, while coerulescine [12] is an oxindole alkaloid isolated from Phalaris coerulescens ( Figure 3). Likewise, maremycins [13] and spirotryprostatin B [14] have been isolated from marine Streptomyces and from the fermentation broth of Aspergillus fumigatus. Among benzo-fused γ-lactam chemical entities, natural and synthetic isoindolinones are a prominent class of compounds. Molecules containing the isoindolinone moiety are of pharmaceuti-cal interest as anxiolytic (pazinaclone [15], pagoclone [16], and JM1232 [17]), anticancer (lenalidomide) [18], anti-inflammatory (indoprofen) [19] and antibiotic agents (lactonamycin) [20] ( Figure 4). In addition, some isoindolinone derivatives show a large variety of biological activities [21][22][23], such as COX-2 inhibition [24], glucokinase activation [25], sodium channel blocking [26], antimycobacterial [27], antiproliferative [28] or carbonic anhydrase inhibition [29], as well as antifungal and antibacterial properties [30]. Isomeric 2-oxindoles are another family of aromatic-fused heterocycles containing the γ-lactam unit. These molecules are often biologically active and therefore, they have found many applications in medicinal chemistry. For example, ropinirole [31] is used in the treatment of early Parkinson's disease, nintedanib is employed against pulmonary fibrosis [32], tenidap [33] is a nonsteroidal anti-inflammatory drug (NSAID), while indolidan [34] and adibendan [35] are potent long-acting cardiotonic agents and SM-130686 is a GHSR agonist [36] ( Figure 5). Other kinase inhibitors such as sunitinib [37] and toceranib [38] are also found in the market for the treatment of several tumours ( Figure 5) and some others are under development or have been entered clinical trials [39]. There are also natural spirooxindole-containing complex molecules that have shown potential medicinal applications, such as NITD609, that shows antimalarial activity [40] and satavaptan, a selective V2-receptor antagonist that is useful for the treatment of cirrhosis ( Figure 5) [41,42]. Additionally, methisazone is a 2-oxindole derivative that has been used as antiviral drug, especially for the prophylactic treatment of small-pox since 1965 [43] and citrinadins A and B have shown activity against murine leukaemia and human epidermoid carcinoma [44], while PF1270 A, B and C act as histamine H3 receptor ligands and, consequently, can be of therapeutic interest to treat diabetes, obesity and central nervous system disorders [45]. Besides, several hybrid molecules containing, inter alia the oxindole moiety, have been discovered and they demonstrated diverse therapeutic activities, for example, against breast [46] and colon cancer cells [47] and drug-resistant bacteria [48].
Among the many excellent recent reviews on the preparation of heterocycles by multicomponent reactions (MCRs) [49][50][51][52][53][54][55], the synthesis of three-and four-membered heterocycles through MCRs has been reviewed recently [56], and taking into account the increasing amount of procedures developed in the last years for the preparation of heterocycles [57,58] with interest in medicinal chemistry [59], such as those devoted to the synthesis of 5-membered γ-lactam heterocycles by means of multicomponent protocols [60], we believe that this field also deserves an in-depth revision that would benefit the researchers working in the synthesis of heterocycles. Especially interesting are the applications of these MCRs [61][62][63][64] in combinatorial chemistry [65] and diversity-oriented synthesis [66], where structurally diverse compound libraries can be rapidly synthesized.
Therefore, this article reviews the procedures disclosed recently for the multicomponent synthesis of isoindolinones II and 2-oxindoles III (Figure 1), where the setup of the γ-lactam core takes place during the key process.
MCRs involve the simultaneous reaction between three or more reactants to deliver products that include significant fragments of all the substrates in their structure. Those starting materials must be added all together in the reaction container and, therefore, other approaches [67][68][69] featuring sequential (domino, tandem or cascade) [70,71] reactions, where one intermediate is initially preformed before additional reagents are added, are not included in this review.

Review Isoindolinones
An extensive range of synthetic methods have been developed for the preparation of isoindolinone derivatives [72][73][74][75], although only a few make use of multicomponent approaches.
Most of the multicomponent syntheses of this type of heterocycles employ a benzoic acid derivative as one of the substrates of the reaction, together with an amine and a third reagent that provides the carbon atom needed to complete the cyclic moiety.
Thus, Shi et al. [76] reacted benzoic acid derivatives 1, amides 2 and DMSO (3) in the presence of DDQ as oxidant and without any metal catalyst. Through a tandem three-component cross-dehydrogenative coupling (CDC), they prepared, in a single step, more than thirty isoindolinone derivatives 4, including those originated from sulfonamides and carboxamides (Scheme 1). The scope of the reaction includes aromatic, some aliphatic and one heteroaromatic derivative with yields ranging from moderate to good. It is remarkable that no catalysts are needed in this transformation. Unfortunately, other aromatic acids bearing substituents different from three methoxy groups did not produce any detectable amounts of isoindolinone.
Based on several additional experiments, the authors propose a tentative mechanism based on a Pummerer-type rearrangement. First, dimethyl sulfoxide (3) and carboxylic acid 1 combine to render ester 5 that decomposes, giving a thionium derivative of DMSO (6, Scheme 1). This electrophilic derivative would react with the nucleophilic aromatic ring in a Friedel-Crafts alkylation process, thus incorporating the carbon atom in a formal C(sp 2 )-H/C(sp 3 )-H cross-dehydrogenative coupling. Finally, an oxidation of sulfide 7 to sulfoxide 8 and the subsequent attack of amide 2 with cleavage of the C-S bond and formation of 9, followed by an intramolecular cyclic amide formation, would produce isoindolinone derivatives 4.
Employing benzoic acids 10 ortho-substituted with iodine along with alkynylcarboxylic acids 11 and ammonium acetate (12), in the presence of caesium carbonate and copper iodide as catalyst (10%), a series of 3-methyleneisoindolin-1-ones 13 were obtained (Scheme 2) [77]. Several aromatic and heteroaromatic substituents can be introduced in the exocyclic methylene position with high regioselectivity. It is noteworthy that arylalkynylcarboxilic acids 11 (R 2 = Ar) can be obtained easily by the coupling reaction of propiolic acid and aryl halides [78].
Furthermore, the authors have been able to carry out the reaction in a sequential manner starting from propiolic acid and aryl iodides in the presence of caesium carbonate and a palladium catalyst. Next, addition of 2-iodobenzoic acid and ammonium acetate leads to the formation of isoindolinone derivative 13 in 55-65% global yields, without isolating any intermediate.
Regarding the reaction mechanism, the authors have ruled out that phthalide must be an intermediate of the reaction and they proposed the two pathways illustrated in Scheme 3. In the first one (path A), decarboxylative coupling to form intermediates 14 and 15, followed by a cyclization take place, while in the second path (B), the first step seems to be the formation of amide 16. Indeed, another multicomponent approach to isoindolinones uses iodobenzamides 17 as starting materials (Scheme 4). In this case, copper catalyst and alkynes are also used but, unlike the above method, alkynes 18 are monosubstituted. The third component is an indole or pyrrole derivative 19 and the result of the reaction is a 3,3-disubstituted isoindolinone derivative 20, which contains a newly formed quaternary centre [79].
The reaction takes places in water, even in the presence of air, and with nanodomain cuprous oxide as an inexpensive and reusable catalyst. The scope includes aryl, alkyl and carboxyl groups at 2-and 3-positions of the lactam ring. Pyrrole reacts across the 2-carbon while indole derivatives do it through the carbon at 3-position. Although a quaternary stereocentre is created in the process, no attempts to make this synthesis in a stereoselective fashion were reported.
A tentative mechanism is proposed, based in a Sonogashira coupling of iodobenzamide 17 and copper acetylide, in a similar way to that described in Scheme 3. In this case, the coupled alkyne moiety is again activated by Cu(I) and then basepromoted cyclization occurs. A new copper complex formation with the alkene analogue to 13 (see Scheme 3) facilitates the aromatic nucleophilic substitution by indole or pyrrole, leading to final lactams 20.
This mechanism is partially corroborated by the following multicomponent synthesis where benzamide 21, ortho-functionalized with a terminal alkyne group (Scheme 5), a secondary amine 22 and carbon monoxide (23) react to produce 3-methyleneisoindolinones 24 [80]. A palladium catalyst in acetonitrile, and a high pressure of both, CO and air, are needed in order to perform an oxidative carbonylation on 2-ethynylbenzamide 21.
Up to ten compounds were obtained with yields ranging from 65 to 96%. Butyl, phenyl, benzyl or absence of substitution on the amide nitrogen produced, in most of the cases, the Z-isomer as the sole or main product, while tert-butyl derivatives gave the E-isomer selectively. On the secondary amine side, morpholine, piperidine, pyrrolidine and dibutylamine all rendered the reaction efficiently.
A plausible explanation for the mechanism of this transformation implies initial formation of an alkynylpalladium intermediate 25 followed by carbonylation to render acylpalladium 26 (Scheme 6). Reductive substitution of palladium by amine 22 furnishes diamide derivative 27 and Pd(0), which is reoxidized to Pd(II) again by HI and oxygen. Then, intramolecular conjugate addition of benzamide nitrogen onto the 2-ynamide generates the final cyclization product 24 through allene intermediate 28. Taking into account that the reaction does not take place with internal alkynes, the authors conclude that a terminal alkyne is necessary for the formation of the first alkynylpalladium complex 25 in the proposed pathway.
Other benzoic acid derivatives such as those bearing a formyl substituent at the ortho position also take part in several multicomponent cyclizations leading to isoindolinones. Thus, 2-formylbenzoate 29, primary amines 2 and terminal alkynes 18 react under copper catalysis to furnish several propargylisoindolinones 30 with modest to good yields (Scheme 7) [81]. Although aryl-and alkylacetylenes can be used in this method, only aromatic amines 2 which are not ortho-substituted work well under these reaction conditions. The reaction probably takes place through an addition of copper acetylide, generated from terminal alkyne and copper, to the imine formed by the reaction between the amine and the formyl group. Then, the secondary propargylamine intermediate would act as a nucleophile in a cyclization process to form the lactam ring.
The same formylbenzoate 29 has also been used in another three-component synthesis along with amines 2 and ketones 31 (Scheme 8) [82]. This Mannich/lactamization reaction achieves good yields for a broad scope of 3-substituted isoindolinones 32, in either catalyst-free conditions or using p-toluenesulfonic acid. Orthoand meta-substituted anilines 2 did not produce isoindolinones 32, and aliphatic amines only reacted when p-toluenesulfonic acid was present. The reaction has also been applied to 1,3-dicarbonyl compounds, however, only residual amounts of isoindolinones 32 were detected and deamination products became predominant. Similarly to the above mentioned method, the first step in this approach is probably the imine formation by reaction of amine 2 with the aldehyde functionality of benzoate 29. Next, addition of the enol form of ketone 31 onto the imine would provide a Mannich intermediate amine, which can intramolecularly attack the ester function, giving rise to lactam 32.
As pointed out above, unfortunately this methodology did not work properly when it was first applied to 1,3-dicarbonyl compounds. Nevertheless, more recently, two research groups have disclosed, nearly simultaneously, the three-component cyclization of 2-formylbenzoic acids, primary amines and a 1,3-dicarbonyl compounds.
The first proposal uses 2-formylbenzoic acid 33 (R = H, conditions A, Scheme 9), cyclic aliphatic and aromatic diketones 34 such as dimedone (R 2 R 3 = -CH 2 CMe 2 CH 2 -) as the 1,3-dicarbonyl partner and a variety of aromatic, heteroaromatic and ali-phatic amines in ethanol, under microwave heating, and without metal catalyst [83]. Very good yields of 35 are obtained in a very simple and cost-effective manner. A rather similar approach was disclosed shortly later by Han and co-workers [84], who used β-ketoacids (34 R 3 = OH, conditions B, Scheme 9) instead of diketones and a quaternary ammonium salt as catalyst in water. In this multicomponent decarboxylative alkylation/cyclization process, they prepared several lactam derivatives 36 with good yields.
While the first research group suggests that the reaction would start with the formation of an imine intermediate between the aldehyde function of 33 and the amine 2, followed by a nucleophilic attack by the diketone and a final intramolecular cyclization, the Han group proposes a different pathway, with an initial deprotonation of ketoacid 34 (R 2 = Me, Ar, R 3 = OH) and a subsequent addition of enolate 37 onto the aldehyde moiety in 33, with concomitant decarboxylation and cyclization to form a phthalide intermediate 38 (Scheme 10). Then, the known amine-substitution reaction would transform phthalide 38 into isoindolinone 36.
A conceptually very similar procedure has been described by Singh and co-workers [85], who used formylbenzoate 29 and preformed enol ethers instead of ketones in a Mukaiyama-Mannich lactamization reaction catalysed by zinc or copper under mild conditions. A large amount of diverse iso-Scheme 10: Proposed mechanism for the formation of isoindolinones 36.
indolinones 32 (thirty-four examples) can be built in this manner, although, once again, ortho-substituted anilines 2 did not render the cyclic product, as the final lactamization step is probably impeded by sterical reasons. On the other hand, silyl enol ethers of acetone, acetophenone, methyl acetate, 2-hydroxyfuran and cyclohexanone worked well, providing isoindolinone 32 with yields ranging from 64 to 85%.
A variation of the above approach that makes use of fluorinated silyl ethers 39, has been applied to the synthesis of analogous fluorinated isoindolinones 40 (Scheme 11) [86]. In this case, formylbenzoic acid 33, a variety of aromatic, aliphatic and heteroaromatic amines 2 and trimethylsilyl enol ethers 39 are combined in a three-component Mannich/lactamization reaction in the presence of an indium catalyst to yield twenty four 3-difluoroalkylisoindolinone derivatives 40. The starting 2-formylbenzoic acid 33 has been also employed in Ugi-type multicomponent reactions with amines and isocyanides by several research groups to make highly functio-nalized lactams. After the pioneering works by Ley [87] and Zhang [88], other contributions have been reported in the last years. For example, Shaabani et al. [89] used diamines 41, isocyanides 42 and two equivalents of 2-formylbenzoic acid (33) in an Ugi three-component reaction with methanol as solvent at room temperature to afford tetrahydrodiisoindoloquinoxalinecarboxamides 43 (Scheme 12). More recently, Shafiee et al. [90] utilized propargylamine as the cycle-nitrogen delivering component and then submitted the obtained isoindolinones 44 (route A, Scheme 13) to an additional cyclization to furnish a pyrazinoisoindoledione derivative. Kajanus and co-workers [91] prepared eight isoindolinone derivatives 45 by this method with yields ranging from 32 to 79% (route B, Scheme 13).
They also made several analogues of these compounds by a sequential Ugi/Diels-Alder approach and, in this context, they were able to separate the enantiomers using chiral chromatography. Some of these compounds showed good in vitro potency blocking the cardiac ion channel Kv1.5 and, therefore, are promising agents to treat atrial fibrillation. Nevertheless, the most outstanding contribution is the first enantioselective Ugi synthesis of isoindolinones 46 catalysed by a chiral phosphoric acid, reported by D.-X. Wang, M.-X. Wang, J. Zhu and co-workers (route C, Scheme 13) [92]. They obtained very good yields and remarkable enantiomeric excesses, which result, according to the authors, from a dynamic kinetic resolution of the initially formed Ugi adduct. amine 50 tautomerization seems to happen faster than the Mumm rearrangement that would lead to isoindolinone 46 through the bridged intermediate 51. Therefore, this mechanistic path shows that the enantioselectivity of the reaction is a consequence of a dynamic kinetic resolution of enamine 50.
Cyanide can also be used, instead of isocyanide, in an analogous three-component reaction, to afford isoindolinones 53 substituted with nitrile or carboxamide groups (Scheme 15, method A) [93]. Trimethylsilylcyanide (52), and benzyl-, alkyland allylamines 2 were reacted with 2-formylbenzoic acid (33) in the presence of OSU-6, a mesoporous silica performing as a green Lewis acid catalyst for this transformation. At room tem-perature, the product of this environmentally friendly Strecker reaction is nitrile derivative 53 (R 2 = CN, Scheme 15, method A), while at reflux carboxamide 53 (R 2 = CONH 2 , Scheme 15, method A) is obtained. Notoriously, aromatic amines 2 did not work under these conditions and, in place of isoindolinones 53, isobenzofuranones were isolated. The method was extended to the corresponding acetophenone derivative 54 and, in this case, quaternary nitriles and carboxamides 55 were prepared in good yields (Scheme 15, method B).
On the contrary, another Strecker multicomponent synthesis, between 2-formylbenzoate 29, benzylamine and potassium cyanide, carried out under mechanochemical conditions and zinc catalysis, only produced a 31% yield of the corresponding cyanoisoindolinone 53a (R 1 = Bn), along with 34% yield of benzyl phthalimide, probably formed by air oxidation of 53a [95]. (33) has also been used in another type of three-component cyclization, along with amines 2 and isatoic anhydrides 56, leading to isoindoloquinazolinone derivatives 57, a kind of heterocycle containing five-and six-membered fused N-heterocyclic rings (Scheme 16), including the γ-lactam unit. The first synthesis of this class of compounds was reported by Pal et al. [96] with the aid of montmorillonite K10 as a recyclable catalyst in ethanol. With these environmentally friendly conditions, they reported the preparation of twelve analogues of 57 with good yields (72-95%, R 1 = H, R 2 = alkyl, benzyl, aryl) (route A, Scheme 16). Some of these molecules were able to inhibit tumour necrosis factor-alpha (TNF-α) in vitro, therefore, showing potential medicinal applications.

2-Formylbenzoic acid
A similar synthetic approach was applied by another research group, using acetic acid instead of ethanol as a solvent and without any other catalyst (route B, Scheme 16) [97]. By this way, seventeen compounds of type 57 were obtained with yields ranging from 80 to 92% (R 1 = H, R 2 = H, alkyl, benzyl, aryl). Another improvement on this multicomponent approach, making use of β-cyclodextrine as promoter, water as a solvent, and microwave heating (route C, Scheme 16) [98]. Under these neutral conditions, they prepared up to nineteen compounds (60-95%, R 1 = H, Cl, R 2 = alkyl, benzyl, aryl), including two derivatives containing chlorine atoms in the portion coming from isatoic anhydride 56.
In all cases, the most likely mechanism is initiated by a nucleophilic attack of amine 2 onto the anhydride carbonyl with opening of the cycle to form carbamic acid derivative 58 and loss of CO 2  A variation of the previous procedure has been disclosed, where 2-formylbenzoic acid (33) is replaced by bromoisobenzofura-none 61, also leading to isoindoloquinazoline derivatives 57 (Scheme 18) [99]. After optimization of the reaction conditions, a 4:1 combination of water and PEG-400 was chosen as the best solvent and an array of nineteen isoindoloquinazolinones 57 with yields ranging from 66 to 92% was prepared. The mechanism is presumably very similar to that of the above reaction (Scheme 17), where isobenzofuranone 61 plays the role of formylbenzoic acid 33. Another multicomponent approach to isoindoloquinazolinones 57 is the palladium-catalysed reaction of 2-aminoamides 59, 2-bromobenzaldehydes 62 and carbon monoxide (23) at atmospheric pressure, with the assistance of DABCO as base and tri(tert-butyl)phosphonium tetrafluoroborate as ligand (Scheme 19) [100]. A variety of substituents in the benzene rings (R 1 , R 3 ) are compatible with the reaction conditions, but heteroaromatic analogues of aldehyde 62, such as 2-bromonicotinaldehyde or 2-bromothiophene-3-carbaldehyde did not produce the desired product. On the other hand, 2-aminoquinoline-3-carboxamide also reacted under these conditions to produce the corresponding isoindoloquinazolinone analogue of 57. Up to 24 isoindolinone derivatives were obtained, bearing a wide variety of aryl moieties at the sulfonyl group, including a thiophene derivative. With the aid of several dedicated experiments, the researchers proposed a mechanism initiated by the formation of an arylsulfonyl radical 72, which then would add to the alkene moiety in 67 to produce a radical intermediate 73 (Scheme 22). The photocatalyst-assisted oxidation of this radical would give rise to the corresponding cation 74, which  Ortho-functionalized benzoic acids have also been prepared in situ and used for a three-component transition-metal-free synthesis of phthalimides 79 induced by fluoride (Scheme 23) [102]. The reaction makes use of 2-(trimethylsilyl)aryl triflates 77, isocyanides 42 and CO 2 (78), and takes place in acetonitrile as solvent and without the need of any transition metal. Different symmetrically and unsymmetrically substituted aryne pre-cursors 77 and alkyl and aryl isocyanides 42 produced thirteen benzamide derivatives 79, with moderate to good yields.  Although most multicomponent reactions leading to isoindolinones make use of benzoic acid derivatives as one of the starting components, in a few contributions aromatic aldehyde, imine or nitrile compounds have been used instead. The scope of the reaction is very wide, since the three components have demonstrated the ability to be efficient sources of diversity in this reaction. Indeed, 33 isoindolinones 88 were prepared with yields ranging from moderate to very good. Even when unsymmetrical diaryliodonium salts 87 were used, the reaction was chemoselective, furnishing in good yields the products resulting from the transfer of the less hindered arene. However, this methodology exhibits two main limitations. First, arenes 86 with electron-withdrawing groups did not react under the optimized conditions and on the other hand, the atom economy is quite low, since a half of the diaryliodonium salt 87 is lost in the process.
Replacing the arene substrate 86 by ketones, and keeping nearly equal reaction conditions, the same authors have achieved an efficient synthesis of 3-(2-oxopropyl)-or pentacyclic isoindolinones 90 or 92 (Scheme 26). Starting from several aryl and aliphatic ketones 89, more than thirty isoindolinones 90 were obtained, with three points of diversity around the lactam core. Overall, aryl ketones containing electron-donating and electronwithdrawing functions and even a heteroaryl group delivered better yields than dialkyl ones (Scheme 26, path A) [104]. When cyclopropyl ketones 91 were used as substrates, a ring expansion and a new quaternary centre formation happened through the multicomponent reaction to produce pentacyclic derivatives 92 (Scheme 26, path B) [105]. the so-obtained furane derivative 96 would add to the carbocation in 95, followed by Friedel-Crafts cyclization, thus generating the polycyclic isoindolinones 92 in a formal hetero [4 + 2] cycloaddition process.
Another aromatic aldehyde, in this case derived from a quinoline, can also be used as substrate for a multicomponent reaction, appropriate for the preparation of 3-aminoisoindolinone analogues 98 (Scheme 28) [106]. Indeed, the reaction of chloroquinolinecarbaldehydes 97 with isocyanides 42 and aromatic amines 2, catalysed by Pd, produced a small collection (8 examples, 75-95% yield) of quinoline derivatives 98 containing a γ-lactam moiety with different substituents at the nitrogen of the 5-membered ring and in the γ-position. Although the authors do not suggest a mechanism, this probably starts with the formation of an imine by reaction of aromatic amine 2 with quinolinecarbaldehyde 97.
Certainly this is a quite feasible hypothesis, since it has been reported that ortho-iodo-substituted arylimines 100, analogues of quinolinecarbaldehyde 97, also reacted, under Pd catalysis, with CO (23) and imines 99 to furnish complex spirocyclic γ-lactams 101 (Scheme 29) [107]. These products show a trans orientation of the benzene moiety in the isoindolinone and the substitu- The proposed mechanism involves an initial palladium-catalysed carbonylation of iodoarylimine 100 to produce acid chloride 102 (Scheme 29). Intramolecular nucleophilic attack of the imine onto the acyl chloride would furnish cyclic N-acyliminium derivative 103, which can then undergo a second palladium-catalysed carbonylation to form a stabilized ketene 104. This is a good partner for a cycloaddition with an imine such as 99 that would give rise to the spiro β-and γ-lactam derivative 101 in a diastereoselective manner.
Indeed, a seminal contribution also made use of a similar Pd-catalysed carbonylation followed by amide formation and cyclization in a three-component reaction between aryl iodides, incorporating a Michael acceptor 105, amines and amides 2 and carbon monoxide (23) (Scheme 30) [108].
It is remarkable that not only aromatic but also aliphatic amines and even amides and sulfonamides can be used as the nitrogencontaining substrate. With chiral amines, very low diastereoselectivity was obtained, probably due to the harsh reaction conditions employed. In addition to carbonyl and carboxyl derivatives, pyridine was also used successfully as an electron-withdrawing group (EWG) in the Michael acceptor 105. A simple control experiment allowed the authors to propose that the first stage of the reaction would be the insertion of carbon monoxide into the Ar-I bond to produce aryl iodide 107, followed by the reaction with the nitrogen nucleophile to form amide intermediate 108. Finally, intramolecular Michael addition would furnish lactam unit 106.

Oxindoles
The simplest protocol for the multicomponent assembly of oxindole heterocycles is the palladium-catalysed reaction involving carbon monoxide, in addition to terminal alkynes, arylboronic acids and alkyl iodides, which has been applied to the preparation of fluorinated 3-methyleneoxindole derivatives (Scheme 31) [109]. In this three-component reaction, 2-ethynylanilines 109 reacted with carbon monoxide (23) and perfluoroalkyl iodides 110, in the presence of Pd(II) and phenylboronic acid (111), by means of an intramolecular amino-carbonylation reaction. Although phenylboronic acid did not incorporate into the final product structure, it was necessary for the reaction to take place. Using this protocol five oxindole derivatives 112 were synthesized with moderate yields, including one substrate containing a 13 C-labelled carbon, suitable to be used as a metabolic tracer.  [110]. In this way, a variety of (2-oxoindolin-3-yl)methanesulfonohydrazides 115 with diverse substituents in the aromatic ring and hydrazine nitrogen, were prepared with moderate to good yields. The same acrylamide 113 (R 1 = H) has been recently used in another multicomponent synthesis along with CO (23) and benzodiazepine derivative 121 under palladium catalysis to give a 1:1 mixture of diastereoisomers of oxindole 122 with good yield (Scheme 34) [111]. In this case, the process consists in a palladium-catalysed cyclization followed by a carbonylation and anion capture. Several analogues of (2-oxoindolin-3-yl)methanesulfonohydrazides 115 have been prepared by another type of three-component approach, in this case under copper catalysis (Scheme 35) [112]. The partners of the reaction are N-(arylsulfonyl)acrylamides 123, aryldiazonium tetrafluoroborates 68 and DABCO·(SO 2 ) 2 (69), as a source of sulfur dioxide. In this way, sulfonated oxindoles 124 are prepared in moderate to good yields.
A wide scope of aryldiazonium reagents 68 bearing electron-donating and electron-withdrawing groups worked well in the reaction, but when a pyridyl heterocycle was employed, the reaction failed. On the acrylamide side, activating and deactivating groups worked similarly well and even a N-heteroaryl analogue of 124 was obtained, although the yield was moderate (42%).
The formation of compound 124 may be explained by a radical process, starting with the addition of arylsulfonyl radical 72, formed from 69 and aryldiazonium cation 68, onto the alkene moiety of sulfonylacrylamide 123 (Scheme 36). Then, ipsocyclization of radical 125 to 126, departure of SO 2 and final oxidation of 127 by Cu(II) would provide oxindole 124. As a consequence of this desulfonylative 1,4-aryl migration, the SO 2 group initially present in the starting acrylamide is replaced by another SO 2 moiety coming from the DABCO·(SO 2 ) 2 reagent.  Other analogues of acrylamides that are appropriate substrates for oxindole preparation using multicomponent protocols are N-arylpropiolamides. This approach has been reported by Seo and co-workers in a series of papers that develop a three-component transformation comprising three palladium-catalysed reactions: Sonogashira, Heck and Suzuki-Miyaura (Scheme 37) [113][114][115]. In this methodology, N-arylpropiolamides 128 reacted with aryl iodides 129 and aryl-or styrylboronic acids 130 under microwave activation to yield 3-(diaryl- Initially [114,115], using arylboronic acids 130 (R = Ar 2 ), a variety of twenty-one diarylmethylene oxindoles 131 were obtained with good yields. When aryl iodide and arylboronic acids bearing different substituents are used, the expected stereochemistry of the asymmetric products 131 is mainly obtained, where the aromatic group coming from the boronic acid partner settles far from the carbonyl group. Methoxy, nitro, chloro and acetoxy groups of the aromatic moiety can be located at the ortho, meta and para positions, although 2-nitro derivatives gave low yields or no reaction in some cases. In addition to above mentioned benzene derivatives, heteroaromatic boronic acids also worked well under the reaction conditions and provided high yields of the corresponding oxindoles 131. Finally, switching the N-substituent in the starting propiolamide 128 by a H or a Bn group, did not affect the yield of the reaction, although the stereoselectivities diminished.
Next [113], the authors applied the reaction conditions to the use of styrylboronic acids 130 (R = CH=CHAr), and a collection of eleven 3-(1,3-diarylallylidene)oxindoles 132 were obtained with good yields and controlled stereochemistry (Scheme 37). Indeed, they found that the PPh 3 ligand promoted the formation of the E-isomer as the main compound while the t-BuXPhos ligand induced the preferential formation of the Z-isomer.
As already mentioned before, this transformation is the result of a sequence of three palladium-catalysed reactions (Scheme 38).
The first one is a Sonogashira coupling reaction between the terminal alkyne of propiolamide 128 and aryl iodide 129, which is preferred to the Suzuki-Miyaura reaction between aryl iodide 129 and boronic acid 130 present in the reaction mixture. Then, an internal Heck cyclization reaction between the substituted alkyne and aryl bromide in 133 takes place to form a cyclic palladium intermediate 134 with E-configuration, resulting from a syn-addition mechanism of this step. The addition of a silver salt reduces the probability of isomerization of the double bond, presumably by changing the anionic character of the palladium complex to cationic in intermediate 135. Finally, is worth mentioning an example of a multicomponent synthesis where the benzene moiety is created from non-aromatic substrates. Certainly, this three-component protocol includes an aromatization step in the course of the acid-catalysed reaction of cyclohexa-1,3-dione (136), amines 2 and alkyl acetylenedicarboxylates 137, to produce the final phenolic oxindoles 138 with good yields (Scheme 39) [116].
Up to twenty different oxindole derivatives were prepared with any kind of substituents on the nitrogen atom, including aromatic, benzyl, heteroarylmethyl and alkyl groups.
According to some control experiments, the authors propose a plausible mechanism involving a sequential enamine formation-Michael addition to produce intermediate 139, followed by intramolecular cyclization to 141 and aromatization through species 142 and 143 (Scheme 40). The cyclization step takes place in a regioselective manner, leading to five-membered heterocycle 141 rather than to the formation of six-membered lactam 140. Then, tautomerization followed by aromatization would provide oxindole 138.

Conclusion
Although the utilization of multicomponent reactions in synthesis is not a new deal, in the last years there has been an increased use of this strategy, particularly for the preparation of heterocyclic compounds. This is mainly due to the need to find new efficient methods in order to save raw materials and work time. Without doubt, multicomponent approaches in chemical synthesis take the advantage of those two saving features. This economical profit is especially interesting for the large-scale synthesis in pharmaceutical laboratories and industry.
Nevertheless, among the multicomponent synthetic methods available for the preparation of isoindolinones II and 2-oxindoles III, only one is enantioselective, even though many of the reactions described in this review involve the generation of new chiral centres. This drawback needs to be addressed so that new ligands and organocatalysts can be discovered and applied to the synthesis of enantiomerically pure γ-lactams of this type under smooth and environmentally more benign reaction conditions.
Another area of improvement is the need to more methods for the multicomponent building of the oxindole core, since the few approaches now available depart from complex starting materials. Therefore, it would be highly desirable to develop new protocols in order to increase the structural diversity of oxindole derivatives to be made using simple substrates and reagents.