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Aldehydes induction

A more eflicient and general synthetic procedure is the Masamune reaction of aldehydes with boron enolates of chiral a-silyloxy ketones. A double asymmetric induction generates two new chiral centres with enantioselectivities > 99%. It is again explained by a chair-like six-centre transition state. The repulsive interactions of the bulky cyclohexyl group with the vinylic hydrogen and the boron ligands dictate the approach of the enolate to the aldehyde (S. Masamune, 1981 A). The fi-hydroxy-x-methyl ketones obtained are pure threo products (threo = threose- or threonine-like Fischer formula also termed syn" = planar zig-zag chain with substituents on one side), and the reaction has successfully been applied to macrolide syntheses (S. Masamune, 1981 B). Optically pure threo (= syn") 8-hydroxy-a-methyl carboxylic acids are obtained by desilylation and periodate oxidation (S. Masamune, 1981 A). Chiral 0-((S)-trans-2,5-dimethyl-l-borolanyl) ketene thioketals giving pure erythro (= anti ) diastereomers have also been developed by S. Masamune (1986). [Pg.62]

Inductive and resonance stabilization of carbanions derived by proton abstraction from alkyl substituents a to the ring nitrogen in pyrazines and quinoxalines confers a degree of stability on these species comparable with that observed with enolate anions. The resultant carbanions undergo typical condensation reactions with a variety of electrophilic reagents such as aldehydes, ketones, nitriles, diazonium salts, etc., which makes them of considerable preparative importance. [Pg.166]

Chiral (salene)Ti(IV) complexes, TMSCN. This system is selective for aldehydes the asymmetric induction is dependent upon aldehyde struc-... [Pg.349]

Meyers has demonstrated that chiral oxazolines derived from valine or rert-leucine are also effective auxiliaries for asymmetric additions to naphthalene. These chiral oxazolines (39 and 40) are more readily available than the methoxymethyl substituted compounds (3) described above but provide comparable yields and stereoselectivities in the tandem alkylation reactions. For example, addition of -butyllithium to naphthyl oxazoline 39 followed by treatment of the resulting anion with iodomethane afforded 41 in 99% yield as a 99 1 mixture of diastereomers. The identical transformation of valine derived substrate 40 led to a 97% yield of 42 with 94% de. As described above, sequential treatment of the oxazoline products 41 and 42 with MeOTf, NaBKi and aqueous oxalic acid afforded aldehydes 43 in > 98% ee and 90% ee, respectively. These experiments demonstrate that a chelating (methoxymethyl) group is not necessary for reactions to proceed with high asymmetric induction. [Pg.242]

Chiral boron(III) Lewis acid catalysts have also been used for enantioselective cycloaddition reactions of carbonyl compounds [17]. The chiral acyloxylborane catalysts 9a-9d, which are also efficient catalysts for asymmetric Diels-Alder reactions [17, 18], can also catalyze highly enantioselective cycloaddition reactions of aldehydes with activated dienes. The arylboron catalysts 9b-9c which are air- and moisture-stable have been shown by Yamamoto et al. to induce excellent chiral induction in the cycloaddition reaction between, e.g., benzaldehyde and Danishefsky s dienes such as 2b with up to 95% yield and 97% ee of the cycloaddition product CIS-3b (Scheme 4.9) [17]. [Pg.159]

Haloalkane,. see Alkyl halide Haloform reaction, 854-855 Halogen, inductive effect of, 562 resonance effect of, 563 Halogenation, aldehydes and, 846-848... [Pg.1300]

There are also methods based on the detection of aldehydic substances, for the typical odor and flavor of rancidity seem to be associated with the liberation of aldehydic materials during the oxidative deterioration. The Kreis test (18), perhaps the best known of these methods, consists of treating the fat with concentrated hydrochloric acid and a solution of phloroglucinol. The red color formed is attributed to a condensation product of epihydrin aldehyde with phloroglucinol. Historically, the chief difficulty with this method has been that fats which are not rancid will often give a positive Kreis test. It has been shown that if this test is quantitatively correlated with the induction period... [Pg.56]

Pitfalls are encountered when allowing chiral nonracemic aldehydes to react with chiral, but racemic, reagents having a stereogenic center at the metal-bearing carbon atom, since its chiral induction usually overrides that of the substrate leading to mixtures of two diastereomers in essentially equal amounts26,27 (Sections D.1.3.3.1.4.1., D.1.3.3.3.3.3.2. and D.1.3.3.3.8.2.3.1.). [Pg.214]

The nucleophilic alkenoylation of a-phenyl-substituted aldehydes and ketones with (methyl-substituted) [l-cyano-l-(trimethylsilyloxy)-2-propenyl]lithium proceeds with good 1,2-induction to afford the j> i-hydroxy ketones109. [Pg.243]

I.3.3.3.3.I.3. Relative Asymmetric Induction Reactions of Chiral Aldehydes with Achiral Allylboron Reagents... [Pg.280]

It is interesting to speculate that asymmetric induction may be the consequence of the exo anomeric effect, a stereoelectronic effect that favors the conformation 5 that places the aglycone O-C bond antiperiplanar to the pyran C(1) —C(2) bond7fi. Related asymmetric induction has also been observed in aldehyde addition reactions of the related, but racemic, pinacol (Z)-y-(tetrahydropyranyloxy)allylboronate49. As indicated in the examples above, however, the level of diastereoselectivity is modest and the only application in asymmetric synthesis is Wuts exo-brevicomin synthesis75. [Pg.296]

The synthesis of 10 features the SN2 displacement of the allylic acetate with migration of R2 from the ate complex6. Precursors 9 are prepared by the hydroboration of 3-acetoxy-l-alkynes that are available with very high enantiomeric purity via the asymmetric reduction of the corresponding l-alkyn-3-ones, and a substantial degree of asymmetric induction occurs in the conversion of 9 to 10. Best results, based on the enantioselectivity of reactions of 10 with aldehydes, are obtained when R2 is a bulky group such as isopinocampheyl (79 85 % ee)6. The yields of reactions of 10 with aldehydes are 62-76%. [Pg.314]

Chiral, nonracemic allylboron reagents 1-7 with stereocenters at Cl of the allyl or 2-butenyl unit have been described. Although these optically active a-substituted allylboron reagents are generally less convenient to synthesize than those with conventional auxiliaries (Section 1.3.3.3.3.1.4.), this disadvantage is compensated for by the fact that their reactions with aldehydes often occur with almost 100% asymmetric induction. Thus, the enantiomeric purity as well as the ease of preparation of these chiral a-substituted allylboron reagents are important variables that determine their utility in enantioselective allylboration reactions with achiral aldehydes, and in double asymmetric reactions with chiral aldehydes (Section 1.3.3.3.3.2.4.). [Pg.326]

After 12 hours at 4 kbar. this reaction provided only 35% of a 63 27 mixture of 22 and a compound which was tentatively assigned structure 23. It is assumed that 23 derives from epimerization of 21 prior to reaction with (aS,S,S)-5l0b. Whether this stereochemical assignment is correct or not, this result shows that 5 may have problems with configurationally labile aldehydes in demanding cases of mismatched double diastereosclcction. For further examples of double asymmetric induction with 5 or related reagents, see refs 31, 34 and 47. [Pg.334]

Effective 1,4-asymmetric induction has been observed in reactions between 2-(alkoxyethyl)-2-propenylsilanes and aldehydes. The relative configuration of the product depends on the Lewis acid used. Titanium(IV) chloride, in the presence of diethyl ether, gave 1,4-ijn-products with excellent stereoselectivity with boron trifluoride-diethyl ether complex, the amt-isomer was the major product, but the stereoselectivity was less83. [Pg.355]

Asymmetric induction has been observed in reactions of e-methoxy- and t-hydroxyallyl-stannanes and aldehydes promoted by tin(IV) bromide 25. [Pg.378]

Effective 1,7-asymmetric induction was observed in the analogous reactions between C-hydroxy-allylstannanes and aldehydes, although in this case the free hydroxy group was required126. [Pg.378]

Diallyldialkylstannanes with chiral alkyl substituents on the tin, show variable asymmetric induction in their Lewis acid catalyzed reactions with aldehydes. Using bis-(/f)-2-phenylbutyl-(di-2-propenyl)stannane, enantiomeric excesses of up to 54% were obtained via attack on the / e-face of the aldehyde96. [Pg.379]

However, with aldehydes from which a very high substrate-based asymmetric induction originates12, such as 2-(tetrahydro-2f/-pyranyloxy)propanal or cw-(2J ,3fJ)-2,3-0-isopropylidene-... [Pg.443]

Pinacolone (3,3-dimethyl-2-butanone) adds to aldehydes in an enantioselective manner when advantage of the induction by a C 2-symmetric boron enolate derived by addition of (2/ ,5/ )-l-chloro-2,5-diphenylborolane is taken. In this way, /i-hydroxy ketones, whose absolute configuration is unknown, arc obtained with 32- 84% cc58. [Pg.473]

If a chiral aldehyde, e.g., methyl (27 ,4S)-4-formyl-2-methylpentanoate (syn-1) is attacked by an achiral enolate (see Section 1.3.4.3.1.), the induced stereoselectivity is directed by the aldehyde ( inherent aldehyde selectivity ). Predictions of the stereochemical outcome are possible (at least for 1,2- and 1,3-induction) based on the Cram—Felkin Anh model or Cram s cyclic model (see Sections 1.3.4.3.1. and 1.3.4.3.2.). If, however, the enantiomerically pure aldehyde 1 is allowed to react with both enantiomers of the boron enolate l-rerr-butyldimethylsilyloxy-2-dibutylboranyloxy-1-cyclohexyl-2-butene (2), it must be expected that the diastereofacial selec-tivitics of the aldehyde and enolate will be consonant in one of the combinations ( matched pair 29), but will be dissonant in the other combination ( mismatched pair 29). This would lead to different ratios of the adducts 3a/3b and 4a/4b. [Pg.573]

Chiral imines derived from 1-phenylethanone and (I. Sj-exo-l, 7,7-trimethyIbicyclo-[2.2.1]heptan-2-amine [(S)-isobornylamine], (.S>1-phenylethanamine or (R)-l-(1-naphthyl) ethanamine are transformed into the corresponding (vinylamino)dichloroboranes (e.g., 3) by treatment with trichloroborane and triethylamine in dichloromethane. Reaction of the chiral boron azaenolates with aromatic aldehydes at 25 "C, and subsequent acidic hydrolysis, furnishes aldol adducts with enantiomeric excesses in the range of 2.5 to 47.7%. Significantly lower asymmetric inductions are obtained from additions of the corresponding lithium and magnesium azaenolates. Best results arc achieved using (.S )-isobornylamine as the chiral auxiliary 3. [Pg.599]


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See also in sourсe #XX -- [ Pg.281 , Pg.283 ]




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Aldehydes, a-alkoxy 1,2-asymmetric induction

Inductive effect in aldehydes and ketones

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