Styrene with oxazolines

Clarke and Shannon also supported copper bis(oxazoline) complexes onto the surfaces of inorganic mesoporous materials, such as MCM-41 and MCM-48, through the covalent binding of the ligand, modified by alkoxysilane functionalities [59]. The immobilized catalysts allowed the cyclopropanation of styrene with ethyldiazoacetate to be performed as for the corresponding homogeneous case, and were reused once with almost no loss of activity or selectivity. 

Table 11 Effect of bis(oxazoline) on the aziridination of styrene with zeolite-supported ...

Scheme 6.5 Bis(oxazolines)bithiophene ligands for Cu-catalysed cyclopropanation of styrene with EDA.

In 2004, ruthenium-catalysed asymmetric cyclopropanations of styrene derivatives with diazoesters were also performed by Masson et al., using chiral 2,6-bis(thiazolines)pyridines. These ligands were prepared from dithioesters and commercially available enantiopure 2-aminoalcohols. When the cyclopropanation of styrene with diazoethylacetate was performed with these ligands in the presence of ruthenium, enantioselectivities of up to 85% ee were obtained (Scheme 6.6). The scope of this methodology was extended to various styrene derivatives and to isopropyl diazomethylphosphonate with good yields and enantioselectivities. The comparative evaluation of enantiocontrol for cyclopropanation of styrene with chiral ruthenium-bis(oxazolines), Ru-Pybox, and chiral ruthenium-bis(thiazolines), Ru-thia-Pybox, have shown many similarities with, in some cases, good enantiomeric excesses. The modification... 

Applying these methodologies monomers such as isobutylene, vinyl ethers, styrene and styrenic derivatives, oxazolines, N-vinyl carbazole, etc. can be efficiently polymerized leading to well-defined structures. Compared to anionic polymerization cationic polymerization requires less demanding experimental conditions and can be applied at room temperature or higher in many cases, and a wide variety of monomers with pendant functional groups can be used. Despite the recent developments in cationic polymerization the method cannot be used with the same success for the synthesis of well-defined complex copolymeric architectures. 

Of the cyclopropanation reactions studied, the reaction between styrene and ethyl diazoacetate has become the benchmark for determining the utility of a bis(oxazoline) ligand in cyclopropanations. In 1990, Masamune and co-workers introduced several bis(oxazoline) ligands including 2 and 35-40 as catalysts for the cyclopropanation of styrene with ethyl diazoacetate. The reactive species in these reactions were determined to be the bis(oxazoline) dimers of type 2a and 38a-40a, as shown in Figure 9.10. 

Table 9.3 contains a sampling of various other bis(oxazoline) ligands that have been used in the cyclopropanation reaction of styrene with ethyl diazoacetate (Table 9.3, Fig. 9.15). °... 

TABLE 5.4. Enantioselective Cyclopropanation of Styrene with Oiazo Esters using Bis-oxazoline Copper Catalysts... 

Asymmetric cyclopropanation. Three laboratories have reported that copper complexes of chiral bis(oxazolines) are effective catalysts for asymmetric cyclopropanation of alkenes with diazoacetates. Bis(oxazolines) such as 1 are readily available by condensation of a-amino alcohols with diethyl malonate followed by cyclization, effected with dichlorodimethyltin or thionyl chloride. Cyclopropanation of styrene with ethyl diazoacetate catalyzed by copper complexes of type 1 indicates... 

Highly efficient catalytic asymmetric cyclopropanation can be effected with copper catalysts complexed with ligands of type 2.3 These bis(oxazolines) are prepared by reaction of dimethylmalonyl dichloride with an a-amino alcohol. As in the case of ligands of type 1, particularly high stereoselectivity obtains when R is /-butyl. Cyclopropanation of styrene with ethyl diazoacetate catalyzed by copper complexed with... 

The asymmetric copper-catalyzed aziridination of styrene with /i-toluenesulfonamide, iodosylbenzene, and 2,2-bis[(4d )-/-butyl-l,3-oxazolin-2-yl]propane catalyst (Evans catalyst) provided the aziridine product with an ee comparable with that previously obtained (Scheme 110) <2001JA7707>. 

Table 1 Cyclopropanation of styrene with several diazoacetates using bis[(4S)-(l-methylethyl)oxazolin-2-yl]methane ...

The copper(l) triflate complex of 1 has been evaluated in the asymmetric cyclopropanation of styrene with ethyl diazoacetate (eq 3). The trans- and cis -2-phenylcyclopropane carboxylates were isolated in 88% yield as a 70 30 ratio of diastereomers in 43% and 44% enantioselectivity. These enantioselectivities are not as high as observed with other bis(oxazoline) ligands. 

Enantioselective Cyclopropanation of Alkenes. Cationic Cu complexes of methylenebis(oxazolines) such as (1), which have been developed by Evans and co-workers, are remarkably efficient catalysts for the cyclopropanation of terminal alkenes with diazoacetates. The reaction of styrene with ethyl diazoacetate in the presence of 1 mol % of catalyst, generated in situ from Copper(I) Trifluoromethanesulfonate and ligand (1), affords the (rans -2-phenylcyclopropanecarboxylate in good yield and with 99% ee (eq 3). As with other catalysts, only moderate transicis selectivity is observed. Higher transicis selectivities can be obtained with more bulky esters such as 2,6-di-r-butyl-4-methylphenyl or dicyclohexylmethyl diazoacetate (94 6 and 95 5, respectively). The efficiency of this catalyst system is illustrated by the cyclopropanation of isobutene, which has been carried out on a 0.3 molar scale using 0.1 mol % of catalyst derived firom the (R,R)-enantiomer of ligand (1) (eq 4). The remarkable selectivity of >99% ee exceeds that of Aratani s catalyst which is used in this reaction on an industrial scale. 

Aryl-5,5-bis(oxazolin-2-yl)-l,3-dioxanes 169 have been easily prepared in three steps from diethyl bis(hydroxymethyl)malonate, amino alcohols, and aromatic aldehydes. They have been used for the copper-catalyzed asymmetric cyclopropanation of styrene with ethyl diazoacetate in up to 99% ee for the trawx-cyclopropane (maximum transicis ratio = 77/23) <05TA1415>. The same reaction performed on 2,5-dimethyl-2,4-hexadiene with tert-butyl diazoacetate in the presence of copper catalysts bearing ligand 170, prepared from arylglycines, exhibited remarkable enhancement of the rrawx-selectivity (transicis ratio = 87/13), with 96% ee for the trans product <05JOC3292>. 

PO/styrene copolymer blends have been com-patibilized through crosslinked copolymer formation between acid-functionalized PO and oxazo-line-functionalized PS (Table 5.42). Anhydride-functionalized PO is also effective in these blends since a proportion of acid groups is present from ring-opened anhydride. Oxazoline groups are most frequently introduced into PS by copolymerization of styrene with isopropenyl oxazoline. 

In 2000, Mayoral [78] described the first immobilization of Box on insoluble polymer. For a same ligand, grafting and several methods of polymerization (Scheme 37) were reported in order to compare the catalytic efficiency of these supported ligands after their complexation with Cu. The study was based on immobilization of bis-(oxazoline) 74a-c (Scheme 36) and their corresponding Cu-complexes were tested in the cyclopropanation of styrene with EDA, a well known reaction in homogeneous catalysis [79]. 

After the introduction of chiral Schiff base and semicorrin ligands as enan-tioselective copper catalysts, the next major advance in copper systems is based on bis(oxazoline) ligand 7 (65) and 8 (66) (Scheme 11). With 7, up to 99% ee of cyclopropane was obtained for the cyclopropanation of styrene with EDA. Same enantioselections but higher diastereoselectivity (transrcis = 94 6) was obtained when 2,6-di-Zert-butyl-4-methylphenyl diazoacetate (BDA) was used instead of EDA. It was noted that the catalytic system with 7 was the only copper sys-... 

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