Glycidic esters, ring opening

Glycidic ester, ring opening with aniline, 38 ... 

Oxazolines can be obtained by the Lewis acid catalyzed epoxide ring opening of glycidic esters or amides (e.g., 118) with acetonitrile . Oxazolidines are available from the palladium-catalyzed cycloaddition of vinyl epoxides with imines <00H885> or the samarium-promoted reaction of ketimines (e.g., 120) with unfunctionalized... 

The ring opening of glycidic acids and their derivatives by reactants such as the sodium salt of malonic ester has been reviewed in Russian. ... 

Darzens reaction of (-)-8-phenylmethyl a-chloroacetate (and a-bromoacetate) with various ketones (Scheme 2) yields ctT-glycidic esters (28) with high geometric and diastereofacial selectivity which can be explained in terms of both open-chain or non-chelated antiperiplanar transition state models for the initial aldol-type reaction the ketone approaches the Si-f ce of the Z-enolate such that the phenyl ring of the chiral auxiliary and the enolate portion are face-to-face. Aza-Darzens condensation reaction of iV-benzylideneaniline has also been studied. Kinetically controlled base-promoted lithiation of 3,3-diphenylpropiomesitylene results in Z enolate ratios in the range 94 6 (lithium diisopropylamide) to 50 50 (BuLi), depending on the choice of solvent and temperature. ... 

Epoxides also participate in the Ritter reaction with nitriles. An investigation of the ring opening of several alkyl-substituted glycidic esters and amides 181 showed that this transformation occurs with inversion and is completely regiospecific. ° Esters appeared to be somewhat more reactive than amides. However, phenyl-substituted glycidic esters and amides 184 are almost totally nonstereoselective. In addition, the oxazolines 186 are isolated in low yield due to the propensity of intermediate 185 to generate an aldehyde byproduct 187 (Scheme 8.53). 

However, these conditions have not been applied to other epoxides. Catalysis by the boron trifluoride -diethyl ether complex is very useful for the ring opening of cyano-substituted epoxides " and glycidic esters see the formation of and Table 14. This is demonstrated by the regioselective opening of the epoxide ring in 2,3-dimethyloxirane-2-carbonitrile to provide 3-fluoro-2-hydroxy-2.3-dimcthylbutanonitrile... 

Table 17. Ring Opening of Glycidic Esters with Amine Hydrotluoridcs ...

Ring Opening of Glycidic Ester with Aniline"... 

When NaY was further applied to the ring opening of a glycidic ester, which is susceptible to polymerization, a -substituted a-hydroxy ester (6a) was exclusively obtained without polymerization because NaY is not a very strong acidic or basic catalyst (Table VII). 

Aminolysis of glycidic esters with ammonia generally results in attack at the -position however Ritter-type ring opening of... 

Oxiranecarboxylic acids 41 (glycidic acids) can be converted into a,P epoxy diazomethyl ketones 42 via mixed anhydrides. It was found that photolysis of these compounds in the presence of alcohols gave yhyunsaturated esters 44. It is thought that nucleophilic attack of the alcohol on the ketene 43 results in epoxide ring opening. The E olefin isomer is predominately formed, although small quantities of Z esters are also isolated (< 10%). Conveniently non-racemic, chiral substrates are readily prepared via Sharpless asymmetric epoxidation of allylic alcohol 39, followed by... 

Nishimura, X, Kameyama, A., Sakurai, X, and Nishikubo, X, Synthesis of polyesters carrying norbomadiene (NBD) moieties by the ring-opening copolymerization of glycidic esters containing NBD moieties with carboxyKc anhydrides and their photochemical reactions. Macromolecules, 29, 3818-3825, 1996. 

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