Complex, Titanium-binaphtholate

An alternative reaction, the addition of an olefinic C—H bond to C=0, is catalyzed by Lewis acidic titanium aryloxide complexes chiral binaphthol ligands give high optical yields.96... 

In this procedure, the complex is formed in toluene and can be used over a range of temperatures (0 to -25°C), without any effect upon the enantioselectivity. The originality of this procedure is the amount of water utilized, more than 1 unusual feature of water per sulfide being essential to produce an effective catalyst, both for high enantioselectivity and to retain the catalytic activity of the titanium-binaphthol complex for an extended time. 

Recently, Maruoka and coworkers reported the exploitation of C,iV-cyclic azomethine imines in highly enantiose-lective asymmetric 1,3-dipolar cycloadditions catalyzed by a titanium-binaphtholate (BINOLate) complex, which offers access to pharmaceutically attractive chiral tetrahydroisoqui-nolines and piperidines with a 1,3-diamine unit [13,14]. Not... 

A combination of diethylzinc with sulfonamides 18 or 19 offers another possibility for the enantioselective acetate aldol reaction39,41. The addition of silyl enol ethers to glyoxylates can be directed in a highly enantioselective manner when mediated by the binaphthol derived titanium complex 2040. 

Binaphthol-derived titanium complexes [64], prepared from chiral ligands 65 (Figure 3.13), also performed very well in the cycloadditions of conjugated aldehydes with cyclic and acyclic dienes. Judging from the absolute configurations of endo and exo adducts, this catalyst should cover the re-face of carbonyl on its u tz-coordination to s-trans a,/l-unsaturated aldehydes, and hence dienes should approach selectively from the si-face. 

Scheme 51 summarizes Mikami s synthesis of (R)-35, employing the car-bonyl-ene reaction of isoprene (A) with glyoxylate (B) to give C as catalyzed by a modified binaphthol-titanium complex [77]. 

A variety of substituted binaphthol and bisphenol complexes of titanium and zirconium have also been investigated as ethylene polymerization initiators. Of note, (62) and (63) exhibit activities of 350 gmmol-1 h-1 bar-1 and 1,580 gmmol-1 h-1 bar-1.190-192... 

Binaphthol (BINOL), chiral titanium complexes of, 25 99 Binary alloys... 

A similar nonlinearity is seen in the ene reaction of methyl glyoxylate and a-methylstyrene (Scheme 43) (69). Thus, the reaction catalyzed by a complex in situ formed from dibromo(diisopropoxy)titanium(IV) and (/ )-binaphthol in 33% ee affords the chiral adduct in 91% ee with the same enantioselectivity as would have been obtained had enantiomerically pure binaphthol been used. Molecular weight measurements suggest the catalyst is a dinuclear titanium compound, although the structure has not been elucidated. This nonlinear effect is interpreted by the difference in the dissociation constant of the diastereomeric dimers as... 

A full account5 describes the enantioselective carbonyl-ene reaction of glyoxylate esters catalyzed by a binaphthol-derived chiral titanium complex that is potentially useful for the asymmetric synthesis of a-hydroxy esters of biological and synthetic importance.6 The present procedure is applicable to a variety of 1,1-disubstituted olefins to provide ene products in extremely high enantiomeric purity by the judicious choice of the dichloro or dibromo chiral catalyst (see Table). In certain glyoxylate-ene reactions involving removal of a methyl hydrogen, the dichloro catalyst... 

Uemura et al. [49] found that (R)-1,1 -binaphthol could replace (7 ,7 )-diethyl tartrate in the water-modified catalyst, giving good results (up to 73% ee) in the oxidation of methyl p-tolyl sulfoxide with f-BuOOH (at -20°C in toluene). The chemical yield was close to 90% with the use of a catalytic amount (10 mol %) of the titanium complex (Ti(0-i-Pr)4/(/ )-binaphthol/H20 = 1 2 20). They studied the effect of added water and found that high enantioselectivity was obtained when using 0.5-3.0 equivalents of water with respect to the sulfide. In the absence of water, enantioselectivity was very low. The beneficial effect of water is clearly established here, but the amount of water needed is much higher than that in the case of the catalyst with diethyl tartrate. They assumed that a mononuclear titanium complex with two binaphthol ligands was involved, in which water affects the structure of the titanium complex and its rate of formation. 

Mikami reported a highly enantioselective carbonyl-ene reaction where a chiral titanium complex 11 prepared from enantiomerically pure binaphthol (BINOL) and Ti(0-i-Pr)2Br2 catalyzed a glyoxylate-ene reaction with a-methylstyrene to give chiral homoallyl alcohol 12 with 94.6% ee [22]. In this reaction, a remarkable asymmetric amplification was observed and almost the same enantioselectivity (94.4% ee) was achieved by using chiral catalyst prepared... 

The asymmetric oxidation of sulphides to chiral sulphoxides with t-butyl hydroperoxide is catalysed very effectively by a titanium complex, produced in situ from a titanium alkoxide and a chiral binaphthol, with enantioselectivities up to 96%342. The Sharpless oxidation of aryl cinnamyl selenides 217 gave a chiral 1-phenyl-2-propen-l-ol (218) via an asymmetric [2,3] sigmatropic shift (Scheme 4)343. For other titanium-catalysed epoxidations, see Section V.D.l on vanadium catalysis. 

K. Mikami, Y. Motoyama, and M. Terada, Asymmetric catalysis of Diels-Alder cycloadditions by an MS-free binaphthol-titanium complex dramatic effect of MS, linear vs positive nonlinear relationship and synthetic applications, J. Am. Chem. Soc., 116 (1994) 2812-2820. 

The outstanding properties of binaphthol (BINOL) as a ligand in chiral Lewis acidic metal complexes were also demonstrated highly successfully by Mikami [108, 109] using a binol-titanium complex 2-69a. Even in the cycloaddition of methyl glyoxylate 2-66 to 1 -methoxy-1,3-butadiene 2-65 which usually shows only a low selectivity, a reasonable cis/trans-selectivity and an excellent enantioselectivity could be obtained in the presence of catalytic amounts of this complex. 

Transformations involving chiral catalysts most efficiently lead to optically active products. The degree of enantioselectivity rather than the efficiency of the catalytic cycle has up to now been in the center of interest. Compared to hydrogenations, catalytic oxidations or C-C bond formations are much more complex processes and still under development. In the case of catalytic additions of dialkyl zinc compounds[l], allylstan-nanes [2], allyl silanes [3], and silyl enolethers [4] to aldehydes, the degree of asymmetric induction is less of a problem than the turnover number and substrate tolerance. Chiral Lewis acids for the enantioselective Mukaiyama reaction have been known for some time [4a - 4c], and recently the binaphthol-titanium complexes 1 [2c - 2e, 2jl and 2 [2b, 2i] have been found to catalyze the addition of allyl stannanes to aldehydes quite efficiently. It has been reported recently that a more active catalyst results upon addition of Me SiSfi-Pr) [2k] or Et2BS( -Pr) [21, 2m] to bi-naphthol-Ti(IV) preparations. 

Vederas and co-workers have reported the ene reaction of an allylglycinate 262 with methyl glyoxylate using copper Lewis acids (Sch. 57) [104], Chiral binaphthol-titanium complexes did not catalyze the ene reaction and only the starting material was recovered. 

Matsuoka, T., Harano, K., Uemura, T., Hisano, T. Hetero Diels-Alder reaction of N-acyl imines. I. The reaction of N -thiobenzoyl-N,N-dimethylformamidine with electron-deficient dienophiles. Stereochemical and mechanistic aspects. Chem. Pharm. Bull. 1993, 41, 50-54. Mikami, K., Motoyama, Y., Terada, M. Asymmetric Catalysis of Diels-Alder Cycloadditions by an MS-Free Binaphthol-Titanium Complex Dramatic Effect of MS, Linear vs Positive Nonlinear Relationship, and Synthetic Applications. J. Am. Chem. Soc. 1994, 116, 2812-2820. 

Aoki, S., Mikami, K., Terada, M., Nakai, T. Enantio- and diastereoselective catalysis of addition reaction of allylic silanes and stannanes to glyoxylates by binaphthol-derived titanium complex. Tetrahedron 1993, 49,1783-1792. 

Oguni has reported asymmetric amplification [12] ((-i-)-NLE) in an asymmetric carbonyl addition reaction of dialkylzinc reagents catalyzed by chiral ami-noalcohols such as l-piperidino-3,3-dimethyl-2-butanol (PDB) (Eq. (7.1)) [13]. Noyori et al. have reported a highly efficient aminoalcohol catalyst, 2S)-3-exo-(dimethylamino)isobomeol (DAIB) [14] and a beautiful investigation of asymmetric amplification in view of the stability and lower catalytic activity of the het-ero-chiral dimer of the zinc aminoalcohol catalyst than the homo-chiral dimer (Fig. 7-5). We have reported a positive non-linear effect in a carbonyl-ene reaction [15] with glyoxylate catalyzed by binaphthol (binol)-derived chiral titanium complex (Eq. (7.2)) [10]. Bolm has also reported (-i-)-NLE in the 1,4-addition reaction of dialkylzinc by the catalysis of nickel complex with pyridyl alcohols [16]. 

Convergent dendrimers, with their versatile three-dimensional scaffold, may be tailored to mimic, perhaps crudely, some elements of enzymatic structures. Numerous catalytic moieties, including manganese porphyrins,253,254 bis(oxazoline) copper complexes,304 305 tertiary amines,306 binaphthol titanium complexes,285 307 titanium taddolates,292,308 thiazolio-cyclophanes,309 and fullerene-bound bisoxazoline copper complexes,310 have been incorporated at the core of dendritic molecules to determine the effect of dendritic encapsulation on their catalytic activity. 

A bimetallic titanium complex of BINOL derivative can be used to catalyze the asymmetric carbonyl-ene reaction [46]. Insoluble polymeric catalyst 74 was prepared from a self-assembly of Ti(OiPr)4 and non-crosshnked copolymers with (R)-binaphthol pendant groups (Scheme 3.22) [47]. The self-assembled polymeric Ti complex is insoluble in organic solvent and catalyzed the carbonyl-ene reaction of glyoxylate 75 and a-methylstyrene 76. When the reaction of 75 and 76 was carried out with 20mol% of 74 in Gl pCf at room temperature, an 85% yield of the product with 88% ee was obtained. Following its recovery by filtration, this catalyst was reused five times with full retenhon of its activity and enantioselectivity, without further treatment... 

An asymmetric Mukaiyama aldol reaction in supercritical fluids using a binaphthol-based titanium complex has also been reported (Scheme 7.43) [113]. 

Mikami K, Matsukawa S, Kayaki Y, Ikariya T. Asymmetric Mukaiyama aldol reaction of a ketene silyl acetal of thioester catalyzed by a binaphthol-titanium complex in supercritical fluoroform. Tetrahedron Lett 2000 41 1931-1934. 

Chiral titanium complexes 4 and 5, which were developed as chiral catalysts for asymmetric carbonyl-ene reactions with prochiral glyoxylate esters [50], were first apphed to the catalytic asymmetric allylation of carbonyl compounds by Mikami and Nakai (Scheme 5) [9]. The titanium catalysts are prepared from (S)-binaphthol and diisopropoxytitanium dihahde (X=C1 and Br) in the presence of 4 A molecular sieves. Using these catalysts, glyoxylates are enantio- and diastereoselectively allylated with allylic trimethylsilanes or allylic tributylstan-nanes. High levels of enantioselectivity and syn selectivity are observed for (E)-crotylsilane and -stannane. The syn selective allylation reaction is believed to proceed mainly through an antiperiplanar transition state. 

Titanium complexes that are similar to Duthaler s ( 2.5.2) can be generated from TiCl4, Ti(Or-Pr)4 and diacetoneglucose 1.48. These complexes catalyze asymmetric hetero-Diels-Alder reactions, and give high enantiomeric excesses [827], Corey and coworkers [828] also prepared a chiral titanium catalyst derived from cis-/V-sulfonyl-2-amino-1 -indanol and used this to catalyze asymmetric Diels-Alder reactions. Buchwald and coworkers [829, 830] have proposed the use of titanocene-binaphthol catalysts for asymmetric hydrogenation of imines or trisubsti-tuted olefins. 

Reactions of a-benzyloxy-, a-chloro- and a-BOCNH acetaldehyde with 6.118 (R = H) are catalyzed by a binaphthol-titanium complex, they are highly enantioselective when conducted in toluene at 0°C [1296], A cyclic silatropic ene pathway has been proposed to interpret these results, with possible chelation of titanium to the heteroatom substituent (Figure 6.99). 

The in situ prepared trialkoxy(chloro)titanium complex is dissolved in CH2C1, (ca. 5 mL per mmol). At -30CC ca. 0.8 equiv of methyl acrylate (5), and after 30 min at the same temperature ca. 2 3 equiv of cyclopcntadiene, are added dropwise. The mixture is kept overnight (ca. 15 h) at - 30 =C, then hydrolyzed with ca. 20 niL of 2 N HC1 and extracted with Ft20. When (R)-binaphthol (7) is used it is extracted with 2 N NaOH. In the case of the 1.3-dioxolanc derivatives it is precipitated by the addition of pentane to the crude reaction mixture, then filtered off. The crude product is purified by flash chromatography. For determination of the oplical rotation a sample is purified by Kugclrohr distillation (130 fC/l 5 Torr). When (3 )-binaphthol (7) is used the adduct is obtained in 77% yield with 50% cc of the (-)-(f )-enantiomer. With the (R.R)-diol 8 derived from tartrate, the (-)-(S)-adduct is predominant (55% yield) with 46% ee. 

This reaction type has been applied to several other aldehydes and dienes and can be used in the synthesis of optically pure natural and non-natural carbohydrate-type systems, such as L-glucose. Hetero-Diels-Alder cycloadditions of this type can also be catalyzed by other chirally modified transition metal complexes, such as CpRu(CH2 = CH2)L3PF6 [L2 = (S)-Chi-raphos, (-)-Diop]68, (binaphthol)TiX269 70 102, vanadium103 104, or carbohydrate-modified titanium catalysts105. 

Molecular sieves (MS) can have a detrimental effect on the enantioselectivity when dienophiles with a free hydroxyl group e.g., juglone (lib) are used. The ee-value drops from 85% for the addition of 1,4-naphlhoquinone (11a) to 1-acetoxy-l,3-butadiene (3c) to 9% for addition of juglone (lib). The latter reaction proceeds with the MS-free binaphthol-titanium complex 21 with 96% ee37. 

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