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Ortho esters formation

In the acyclic derivatives, the possibility of ortho-ester formation between C-l and C-2 would be lessened by a more facile reaction of the carbonyl group with ammonia. [Pg.116]

As a further test, we attempted to convert the 14-OH group to hydrogen in 10, to confirm that the 14-OH group participated in the abstraction of the 2 -hydrogen of dithiane 10. Compound 16 was synthesized from naltrexone methyl ether [22] and then subjected to the same acetal exchange reaction as above. Under the same conditions, acetal 18 was obtained instead of the objective ortho ester (Scheme 4), consistent with our hypothesis that the 14-OH group participated in the ortho ester formation. Subsequently, the obtained ortho ester 12 was readily hydrolyzed with acid to give ester 19 (Scheme 5). [Pg.194]

The addition of methyl groups to the oxetane precursor increases the rate of ortho ester formation by a factor of 22,000 over the OBO derivative and decreases its rate of acid catalyzed hydrolysis by a factor of 2. ... [Pg.628]

Disadvantages multistep procedure requires AgOTf for the ortho esters formation. [Pg.200]

Acylated Corticoids. The corticoid side-chain of (30) was converted iato the cycHc ortho ester (96) by reaction with a lower alkyl ortho ester RC(OR )2 iu benzene solution ia the presence of i ra-toluenesulfonic acid (88). Acid hydrolysis of the product at room temperature led to the formation of the 17-monoesters (97) ia nearly quantitative yield. The 17-monoesters (97) underwent acyl migration to the 21-monoesters (98) on careful heating with. In this way, prednisolone 17a,21-methylorthovalerate was converted quantitatively iato prednisolone 17-valerate, which is a very active antiinflammatory agent (89). The iatermediate ortho esters also are active. Thus, 17a,21-(l -methoxy)-pentyhdenedioxy-l,4-pregnadiene-liP-ol-3,20-dione [(96), R = CH3, R = C Hg] is at least 70 times more potent than prednisolone (89). The above conversions... [Pg.104]

The final stages of the successful drive towards amphotericin B (1) are presented in Scheme 19. Thus, compound 9 is obtained stereoselectively by sodium borohydride reduction of heptaenone 6a as previously described. The formation of the desired glycosida-tion product 81 could be achieved in dilute hexane solution in the presence of a catalytic amount PPTS. The by-product ortho ester 85 was also obtained in approximately an equimolar amount. Deacetylation of 81 at C-2, followed sequentially by oxidation and reduction leads, stereoselectively, to the desired hydroxy compound 83 via ketone 82. The configuration of each of the two hydroxylbearing stereocenters generated by reduction of carbonyls as shown in Scheme 19 (6—>9 and 82->83) were confirmed by conversion of 83 to amphotericin B derivative 5 and comparison with an... [Pg.446]

For a review of the formation of ortho esters by this method, see DeWolfe, R.H. Ref. 500,... [Pg.613]

Again, the Cannizzaro reduction occurs under the condensation conditions. The ortho ester HC(0Et)2 was used as a dehydrating agent in the final acetal format ion. [Pg.210]

Pedersen and coworkers investigated the El mass spectra of several 2-hydroxyphenyl alkyl sulfones (39) and sulfoxides (Section II.B). The methyl derivative seemed to fragment only via sulfinate ester formation giving the primary product ions m/z 157 and 109 (equation 14). Obviously hydrogen bonding between the ortho hydroxyl and the sulfone sulfur makes the loss of CH3SO2 difficult in contrast to the situation in methyl phenyl sulfone. The sulfinate ester rearrangement is not important when R>Et in 39. [Pg.134]

The three-step procedure described for the preparation of the illustrated crotylsilanes is initiated with the hydrosilation of rac-3-butyn-2-ol. This procedure is significantly improved with respect to the positional selectivity of the hydrosilation resulting in exclusive formation of the racemic (E)-vinylsilane, and as a result the present procedure is much more amenable to scale-up than those previously described in the literature.8 The enzymatic resolution of the racemic secondary allylic alcohol (vinylsilane) has also been reported using commercially available lipase extracts. The use of a Johnson ortho ester Claisen rearrangement affords the (E)-crotylsilanes 4 in nearly enantiomerically pure form. [Pg.190]

The influence of temperature on the ortho effect has been evaluated in the alkaline hydrolysis in aqueous DMSO solutions of ortho-, meta- and para-substituted phenyl benzoates (26). The alcoholysis of phthalic anhydride (27) to monoalkyl phthalates (28) occurs through an A-2 mechanism via rate-determining attack of the alcohol on a carbonyl carbon of the anhydride (Scheme 4). Evidence adduced for this proposal included highly negative A 5 values and a p value of 4-2.1. In the same study, titanium tetra-n-butoxide and tri-n-butyltin ethanoxide were shown to act as effective catalysts of the half-ester formation from (27), the mechanism involving alkoxy ligand exchange at the metal as an initial step. ... [Pg.41]

The synthesis of ortho esters from nitriles is usually a two-step process involving first the formation of the imino ester hydrochloride and subsequent reaction with an alcohol. Several examples are described in Table I, even a glycol such as ethylene glycol can be used to obtain heterocyclic ortho esters, as shown in Eq. (11). [Pg.30]

Alkyl formates or formic acid and its esters can be converted to trialkyl orthothioformates [74-77] which in turn can be converted to trialkyl orthoformates in good yields [78, 79], It has been reported that acid chlorides of higher carboxylic acids can also be converted to trialkyl orthothioformates [80], but thus far no reports appear in the literature on attempts to convert them to trialkyl ortho esters. [Pg.34]

The addition of alcohols to ketene acetals allows the synthesis of mixed ortho esters [96, 120a-c, 121a, b, 124, 125a, b]. a-Haloaldehydes may be converted to ortho esters by the following process (a) acetal formation, (b) de-hydrohalogenation, and (c) reaction with alcohols via addition reaction (33). In general, the method above, using ketene acetals, is not practical since ketene acetals are not readily available and are difficult to prepare. However, the method is useful because it allows the synthesis of mixed ortho esters and other ortho esters more difficult to synthesize [122-127]. Recently a simple one-step synthesis of ketene acetals and ortho esters has been reported (see p. 56). [Pg.288]

Formation of mixed ortho esters by a disproportionation reaction between two ortho esters [35]. [Pg.292]

The presence of alkoxide ion would enhance the rate of ammonolysis, and the formation of bis(amido) derivatives by an ortho-ester mechanism (see Section VI, p. 110) would be partially suppressed in the competitive set of reactions. Thus, ammonolysis of penta-O-benzoyl-D-glucose in the presence of 5 mmolar proportions of sodium meth-oxide showed a decrease of 11% in the yield of the bis(benzamido)-glucitol derivative as compared with the same reaction conducted without added methoxide ion.47... [Pg.100]

This point is well-illustrated by the data of Table 19, which show the effect of methyl substituents on the rate coefficients for methyl ester formation from benzoic acid. The compounds fall naturally into three classes. Those with no ortho substituent react 3-4 times as fast as those which have one orthomethyl group, while 2,6-dimethylbenzoic acid, the only compound with two orf/io-substituents, did not give the ester at a measurable rate. [Pg.134]

Orf/io-substituents in general reduce the rates of acid-catalyzed ester formation and hydrolysis. Some typical data are collected in Table 20. In each series the rate coefficient decreases as the size of the ortho substituent increases. Only the smallest substituent of all, the fluorine atom, does not have a marked effect. [Pg.134]


See other pages where Ortho esters formation is mentioned: [Pg.233]    [Pg.233]    [Pg.117]    [Pg.456]    [Pg.456]    [Pg.463]    [Pg.348]    [Pg.75]    [Pg.256]    [Pg.4]    [Pg.19]    [Pg.233]    [Pg.233]    [Pg.117]    [Pg.456]    [Pg.456]    [Pg.463]    [Pg.348]    [Pg.75]    [Pg.256]    [Pg.4]    [Pg.19]    [Pg.7]    [Pg.144]    [Pg.773]    [Pg.134]    [Pg.312]    [Pg.120]    [Pg.191]    [Pg.196]    [Pg.48]    [Pg.697]    [Pg.79]    [Pg.110]    [Pg.258]    [Pg.387]    [Pg.111]    [Pg.116]   
See also in sourсe #XX -- [ Pg.1294 ]




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Ester formation

Esters Formates

Formate esters

Ortho acid esters, formation

Ortho esters

Ortho-formate

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