Epoxides with lithium aluminum

The preparation of Pans-1,2-cyclohexanediol by oxidation of cyclohexene with peroxyformic acid and subsequent hydrolysis of the diol monoformate has been described, and other methods for the preparation of both cis- and trans-l,2-cyclohexanediols were cited. Subsequently the trans diol has been prepared by oxidation of cyclohexene with various peroxy acids, with hydrogen peroxide and selenium dioxide, and with iodine and silver acetate by the Prevost reaction. Alternative methods for preparing the trans isomer are hydroboration of various enol derivatives of cyclohexanone and reduction of Pans-2-cyclohexen-l-ol epoxide with lithium aluminum hydride. cis-1,2-Cyclohexanediol has been prepared by cis hydroxylation of cyclohexene with various reagents or catalysts derived from osmium tetroxide, by solvolysis of Pans-2-halocyclohexanol esters in a manner similar to the Woodward-Prevost reaction, by reduction of cis-2-cyclohexen-l-ol epoxide with lithium aluminum hydride, and by oxymercuration of 2-cyclohexen-l-ol with mercury(II) trifluoro-acetate in the presence of ehloral and subsequent reduction. ... 

Reduction of a sugar epoxide with lithium aluminum hydride also gives a mixture of deoxy sugars in which one isomer may preponderate. This method has been successfully used22 to synthesize a derivative (5) convertible into 2-deoxy-D-erythro-pentose-2(S)-d. 

Corey s procedure. Coxon et al.13a in New Zealand found that the reagent reacts with nopinone (6, numbering of the paper) to give 2/3,10-epoxypinane (7) in high yield. Reduction of this epoxide with lithium aluminum hydride gave lOa-pinane-2j8-ol (5). 

Epoxides are reduced to alcohols on treatment with lithium aluminum hydride Hydride is transferred to the less substituted carbon... 

Another synthesis of the cortisol side chain from a C17-keto-steroid is shown in Figure 20. Treatment of a C3-protected steroid 3,3-ethanedyidimercapto-androst-4-ene-ll,17-dione [112743-82-5] (144) with a tnhaloacetate, 2inc, and a Lewis acid produces (145). Addition of a phenol and potassium carbonate to (145) in refluxing butanone yields the aryl vinyl ether (146). Concomitant reduction of the C20-ester and the Cll-ketone of (146) with lithium aluminum hydride forms (147). Deprotection of the C3-thioketal, followed by treatment of (148) with y /(7-chlotopetben2oic acid, produces epoxide (149). Hydrolysis of (149) under acidic conditions yields cortisol (29) (181). 

The course of the ring opening in epoxides derived from various exocyclic methylene compounds by treatment with lithium aluminum deuteride has been studied in the norbornane series. ... 

The configurations assigned to (8) and (9) were established by comparison with the products resulting from epoxidation of 3-methyl-5a-cholest-2-ene followed by reduction with lithium aluminum hydride to the alcohol (9). The usual /ra 5-diaxial epoxide opening requires that the hydroxyl group, formed by reduction, is axial as shown in (9). 

To overcome this, the A -acetyl group is reduced with lithium aluminum hydride. The resulting basic enamine then reacts extremely rapidly and selectively with peracid. The derived epoxide is hydrolyzed very easily with alkali during the workup. 

Epoxides are reduced by treatment with lithium aluminum hydride to yield alcohols. Propose a mechanism for this reaction. 

The stereochemistry of the first step was ascertained by an X-ray analysis [8] of an isolated oxazaphospholidine 3 (R = Ph). The overall sequence from oxi-rane to aziridine takes place with an excellent retention of chiral integrity. As the stereochemistry of the oxirane esters is determined by the chiral inductor during the Sharpless epoxidation, both enantiomers of aziridine esters can be readily obtained by choosing the desired antipodal tartrate inductor during the epoxidation reaction. It is relevant to note that the required starting allylic alcohols are conveniently prepared by chain elongation of propargyl alcohol as a C3 synthon followed by an appropriate reduction of the triple bond, e. g., with lithium aluminum hydride [6b]. 

Reductive opening of the oxirane ring of 193 with lithium aluminum hydride, and acetylation, provided compound 194. Epoxidation of 194 with mCPB A gave the epoxide 195. Opening of the oxirane ring with acetate ions, followed by acetylation, gave the tetraacetate 196, or, by exhaustive acetylation with acetic anhydride-DMAP, the pentaacetate 189. Compounds 196 and 189 were readily transformed into 190 by hydrolysis. " ... 

Solutions of low-valence titanium chloride (titanium dichloride) are prepared in situ by reduction of solutions of titanium trichloride in tetrahydrofuran or 1,2-dimethoxyethane with lithium aluminum hydride [204, 205], with lithium or potassium [206], with magnesium [207, 208] or with a zinc-copper couple [209,210]. Such solutions effect hydrogenolysis of halogens [208], deoxygenation of epoxides [204] and reduction of aldehydes and ketones to alkenes [205,... 

The synthesis of isomeric DL-allitol succeeded when the hydroxyl groups in cts,cis-2,4-hexadiene-l,6-diol were protected with benzoyl or mesyl groups. Epoxidation gave the appropriate derivatives of 2,3 4,5-dianhydro-DL-allitol (16%), which were then reduced with lithium aluminum hydride to DL-crt/f/iro-2,5-hexanediol. 

Several alioyclio epoxides substituted with polar atoms have been reduced with lithium aluminum hydride, largely by Moueesron and eo-workers, although subsequent investigators3 -1,70 have expressed disagreement with certain of their results. Experimental difficulties in... 

Since the introduction of lithium aluminum hydride for the cleavage of sugar epoxides,M its use in this route to 3-deoxy sugars has become the method of choice. Thus, treatment of methyl 2,3-anhydro-4,6-0-benzyli-dene-a-D-mannopyranoside with lithium aluminum hydride affords methyl... 

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