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Oxazolidines, preparation from

Diastereoselective addition in Et20/HMPT (1 1) leads to the (5)-aldehyde with an enantiomeric excess of 40%, whereas in -hexane the (2 )-aldehyde is formed with 80% ( ) enantiomeric excess. The (2 )-configured aldehyde is also obtained in benzene and in dichloromethane, but with lower ee values of 50% and 25%, respectively. Inverse results were obtained with a chiral oxazolidine prepared from ( )-cinnamaldehyde and (+)-ephedrine. Here, the (5)-aldehyde with ee = 79% is formed in -hexane, and the (7 )-aldehyde in Et20/HMPT (1 1) with ee = 50% [703], This result may be due to different structures of the organocopper reagent, and hence of the diastereomorphic activated complexes, in nonpolar solvents ( -hexane, benzene, dichloromethane) and in EPD solvents (Et20/HMPT) [703]. [Pg.290]

A chiral oxazolidine prepared from a,j6-unsaturated aldehydes and ( —)- or (-l-)-ephedrine efficiently induced asymmetric cyclopropanation with excess of diazomethane in the presence of palladium acetate, e.g. formation of 24 from ( —)-ephedrine and ( )-cinnamaldehyde 24 was cyclopropanated to give 25 and the auxiliary removed giving... [Pg.262]

Oxazolidines are subject to ring-chain tautomerism. A variety of substituted oxazolidines in the solid state exist in the chain form, based on C NMR experiments <85X5919,92X4979). In solution, the two forms are in equilibrium, the position of which depends on the solvent and the substituents. Oxazolidines prepared from meta- and para-substituted benzaldehydes and 2-amino-2-methyl-propanol, norephedrine, norpseudoephedrine, and serine esters all give good linear plots for the equation log -l-log Ax=h where a are the Hammett-Brown values <93X6701,93JOC1967). [Pg.270]

Enantiopure a-amino aldehydes are valuable synthons in natural product synthesis [57]. However, problems are often encountered with their configurational instability [58]. Aziridine-2-carboxaldehydes are also a-amino aldehydes and accordingly have a potential synthetic value. We found that M-tritylaziridine-2-carboxaldehyde 56 is a perfectly stable compound and therefore comparable to Garner s aldehyde (ferf-butyl 2,2-dimethyl-4-(S)-formyl-oxazolidine-3-car-boxylate). Aldehyde 56 can readily be prepared from aziridine-2-carboxylic ester 12 by the sequence shown in Scheme 42 [59]. [Pg.117]

In the presence of a catalytic amount of chiral lanthanide triflate 63, the reaction of 3-acyl-l,3-oxazolidin-2-ones with cyclopentadiene produces Diels-Alder adducts in high yields and high ee. The chiral lanthanide triflate 63 can be prepared from ytterbium triflate, (R)-( I )-binaphthol, and a tertiary amine. Both enantiomers of the cycloaddition product can be prepared via this chiral lanthanide (III) complex-catalyzed reaction using the same chiral source [(R)-(+)-binaphthol] and an appropriately selected achiral ligand. This achiral ligand serves as an additive to stabilize the catalyst in the sense of preventing the catalyst from aging. Asymmetric catalytic aza Diels-Alder reactions can also be carried out successfully under these conditions (Scheme 5-21).19... [Pg.282]

Chiral titanium catalysts have generally been derived from chiral diols. Narasaka and colleagues251 developed an efficient catalyst, 406, prepared from TiCl2(OPr- )2 and a (+)-tartaric acid derived 1,4-diol. These authors found that Af-crotonyl-l,3-oxazolidin-2-one (404) reacted with cyclopentadiene in the presence of 10 mol% of 406 to give cycloadduct 405 with up to 91% ee (equation 120)252. [Pg.421]

Oxazolidin-5-ones (11.110) are structurally related to oxazolidines, combining the motifs of a lactone and an O-Mannich base. These derivatives have already been discussed in Sect. 8.7.5. However, they serve here as a transition to [3,1 ]benzoxazepin-4-ones as an example of potential prodrugs. Thus, [3,l]benzoxazepin-4-one derivatives (11.111, R = H or Me, R = H, Me, Et, or Ph) were prepared from diclofenac (11.112) [137]. These prodrugs were stable for at least a few hours in simulated gastric juice, but, when administered to rats elicited an anti-inflammatory response comparable to that of diclofenac. One compound (11.111, R = Me, R = Et) was even more active than diclofenac without producing the gastric mucosal injury (ulcers) caused in all rats by diclofenac itself. Here again, there was no indication of whether the mechanism of hydrolysis is chemical or enzymatic. [Pg.728]

Sn2 Reactions with epoxides and aziridines are also synthetically useful. An example of epoxide cleavage with an organocopper reagent with sp carbon moieties is the enantioselective synthesis of (3S, 4S)-4-methyl-3-heptanol (53), an elm bark beetle (Scolytus multistriatus) pheromone [42]. The chiral epoxy oxazolidine 51 [43], prepared from (R)-phenylglycinol, reacted with a propylmagnesium bromide-derived cuprate at —70 °C to afford the oxazolidine 52 in 74% yield (Scheme 9.12). Compound 52 was converted into the target molecular 53 by conventional procedures. [Pg.300]

To increase the yields of the ring closure reactions, a new method was developed that was successfully applied for the synthesis of alicyclic fused systems of both the parent oxazolidine-2-thione and tetrahydro-1,3-oxazine-2-thione (85S1149). As an example, the synthesis of 2-thioxoperhydro-l,3-benzoxazine 103 is described. The dithiocarbamate 101, prepared from the amino alcohol 100, carbon disulfide and triethylamine, was treated with ethyl chloroformate in the presence of triethylamine, to give the thioxo derivative 103 via the transition state 102 (85S1149). In this way, the fused-skeleton thioxooxazines (91, X = S, 92) can be prepared with considerably higher yields (50-70%) than by the earlier methods (85S1149). [Pg.365]

Lactol 128 has been converted into a variety of racemic C-nucleosides. The unstable aldehyde 130 was prepared from 128 by way of oxazolidine 129. Lactone 131 was also derived from 128 and used as starting material in the synthesis of racemic C-nucleosides. Adducts 77 + 77 were transformed into epoxide 132. Opening of the epoxide, followed by ozonolysis and reduction allowed one to... [Pg.214]

Furthermore, this reaction was applied to the aldol reaction of 3-pentanone. When the chiral oxazolidine was prepared from 3-pentanone and the aldol reaction was carried out by the same procedure, the a, 6-anti 6-hydroxy ketones were produced predominantly over the syn-isomer 8i with excellent optical purities.(5) (See Table 2.)... [Pg.291]

The first asymmetric synthesis of (-)-monomorine I, an enantiomer of the natural alkaloid, by Husson and co-workers starts with the chiral 2-cyano-6-oxazolopiperidine synthon (385) prepared from (-)-phenylglycinol (384), glu-taraldehyde (383), and KCN (443). Alkylation of 385 with an iodo ketal led to the formation of a single product (386). The cyano acetal (386) was treated with silver tetrafluoroborate and then zinc borohydride to afford a 3 2 mixture of C-6 epimeric oxazolidine (387) having the (2S) configuration. Reaction of 387 with... [Pg.268]

AT-Protected oxazolidin-S-ones 81 can be rapidly prepared from protected amino acids and paraformaldehyde under microwave irradiation <99SC4017>. They undergo several useful... [Pg.228]

Analogous to the use of chiral acetals one can employ chiral N,O-acetals, accessible from a, -unsatu-rated aldehydes and certain chiral amino alcohols, to prepare optically active -substituted aldehydes via subsequent Sn2 addition and hydrolysis. However, the situation is more complicated in this case, since the N,0-acetal center constitutes a new stereogenic center which has to be selectively established. The addition of organocopper compounds to a, -ethylenic oxazolidine derivatives prepared from unsaturated aldehydes and ephedrine was studied.70-78 The (diastereo) selectivities were rather low (<50% ee after hydrolysis) in most cases, the highest value being 80% ee in a single case.73 There is a strong solvent effect in these reactions, e.g. in the addition of lithium dimethylcuprate to the ( )-cinnamaldehyde-derived oxazolidine (70 Scheme 28) 73 the (fl)-aldehyde (71) is formed preferentially in polar solvents, while the (S)-enantiomer [ent-71) is the major product in nonpolar solvents like hexane. This approach was utilized in the preparation of citronellal (80% ee) from crotonaldehyde (40% overall yield).78... [Pg.210]

Kobayashi reported an asymmetric Diels-Alder reaction catalyzed by a chiral lanthanide(III) complex 24, prepared from ytterbium or scandium triflate [ Yb(OTf)3 or Sc(OTf)3], (Zf)-BINOL and tertiary amine (ex. 1,2,6-trimethylpiperidine) [30], A highly enantioselective and endose-lective Diels-Alder reaction of 3-(2-butenoyl)-l,3-oxazolidin-2-one (23) with cyclopentadiene (Scheme 9.13) takes place in the presence of 24. When chiral Sc catalyst 24a was used, asymmetric amplification was observed with regard to the enantiopurity of (/ )-BINOL and that of the endoadduct [31 ]. On the other hand, in the case of chiral Yb catalyst 24b, NLE was affected by additives, that is, when 3-acetyl-l,3-oxazolidin-2-one was added, almost no deviation was observed from linearity, whereas a negative NLE was observed with the addition of 3-pheny-lacetylacetone. [Pg.707]

Despite the similarity between compound 1 and (-)-swainsonine, a different retrosynthetic strategy was devised for the synthesis of (-)-swainsonine (Scheme 3).19 The ring rearrangement yielded the hydropyrrolidine 5, which was prepared from the precursor 6. The enantiometrically pure oxazolidine derivative 7 was a suitable chiral starting material, as it was efficiently synthesised from the diol 8. As with the synthesis of 1, a palladium (0) catalysed allylic amination was carried out in the presence of ligand L (Scheme 2)14 to give 7 with an ee of 97%, which was increased to >99% on recrystallisation with dichloromethane/hexane. [Pg.321]

Enantioselective Diels-Alder reaction. Highly stereoselective Diels-Alder reactions can be achieved by use of the 4,4 -diphenylbis(oxazoline) 2b, prepared from (+)-phenylglycinol, as a chiral, bidentate ligand for iron salts. Thus reaction of Fel3 with 2b and I2 in CH3CN forms a complex presumed to be I-Fel3, which can catalyze reaction of 3-acryloyl-l,3-oxazolidin-2-one with cyclopentadiene at —50° to give the endo-adduct in 95% yield. The product is the 2R-enantiomer (82% ee). [Pg.40]

Stereoselective cyclopropanation.2 Reaction of the chiral oxazolidine 2, prepared from (lR,2S)-norephedrine, reacts with 1 (3 equiv.) in benzene-hexane at... [Pg.191]

During the development of rivaroxaban 1, Pleiss et al. at Bayer Health Care prepared [14C]-radiolabeled rivaroxaban,22 which was required for clinical studies of drug absorption, distribution, metabolism, and excretion (ADME studies). The approach taken for the synthesis of l4C labeled rivaroxaban 38 relies on the previously reported synthesis. In the presence of EDC HCl and HOBT, 4- 4-[5S)-5-(aminomethyl)-2-oxo-l,3-oxazolidin-3-yl]phenyl -morpholin-3-one 22 was coupled with 5-chloro-2-thiophene [14C]-carboxylic acid 37 and was purified using chiral HPLC to afford the [l4C]-radiolabelled rivaroxaban 38 in 85% yield with high chemical and radiochemical purity and with an enantiomeric excess of > 99% ee (Scheme 5). Meanwhile, the metabolite M-4 of rivaroxaban (compound 39) was prepared from 5-chlorothiophenecarboxylic acid chloride 23 and [14C]glycine in 77% yield (Scheme 6). [Pg.202]

Arylsulfonyloxazolidines.1 The optically active oxazolidine 1, prepared from (R)-(N-toluenesulfonyl)phenylglycinol and 2-hydroxymethylenecyclohexanone,... [Pg.242]

Oxazolidines are commonly prepared from /3-amino alcohols and carbonyl compounds (equation 173). The condensation is conveniently conducted in boiling benzene with continuous removal of water. Treatment of 2-aminoethanol with formaldehyde yields the parent compound (67BSF571). An interesting reaction is the formation of the enantiomerically pure oxazolidine (307) from (-)-ephedrine and the alkynic sulfone PhS02C=CMe (79JCS(P1)1430). [Pg.229]

A chiral Diels-Alder catalyst has been prepared from Yb or Sc triflate, (/ )-(+)-binaphthol with a tertiary amine (trimethyl piperidine) catalyzing the reaction of crotonoyl-l,3-oxazolidin-2-one with cyclopentadiene as shown below [ 162,163],... [Pg.955]

Catalytic asymmetric 1,3-dipolar cycloaddition of a nitrone with a dipolarophile has been performed using a chiral scandium catalyst [31]. The chiral catalyst, which was effective in asymmetric Diels-Alder reactions, was readily prepared from Sc(OTf)3, (7 )-(-i-)-BINOL, and d5 -l,2,6-trimethylpiperidine. The reaction of benzylbenzylide-neamine A-oxide with 3-(2-butenoyl)-l,3-oxazolidin-2-one was performed in the presence of the chiral catalyst to yield the desired isoxazolidine in 69 % ee with perfect diastereoselectivity (endolexo = > 99 1) (Sch. 8) [31,46], It was found that reverse enantioselectivity was observed when a chiral Yb catalyst, prepared from Yb(OTf)3, the same (i )-(-i-)-BINOL, and cd-l,2,6-trimethylpiperidine, was used instead of the Sc catalyst under the same reaction conditions. [Pg.895]

Kobayashi and co-workers obtained better selectivity with a chiral Yb catalyst (Table 12) [40]. When Y-benzylidenebenzylamine A/-oxide was reacted with 3-(2-butenoyl)-l,3-oxazolidin-2-one in the presence of a catalyst prepared from Yb(OTf)3, binaphthol and cw-l,2,6-trimethylpiperidine, the corresponding isoxazoline was obtained in 78% ee (entry 3). Interestingly, the addition of A/-methyl-bis[(7 )-l-(l-naphthyl)ethyl]amine ((/ )-MNEA) instead of c/5-l,2,6-trimethylpiperidine resulted in increased ee (96% ee, entry 6) whereas addition of (5)-MNEA gave the adduct in only 62% ee (entry 7). When, moreover, the reaction was conducted in the absence of 4A MS or in the presence of other additives, inversion of the absolute configurations of the products was observed (Table 13, entries 2 and 3) [41], as had been observed... [Pg.929]

Substituted oxazolidin-5-one derivatives, which are prepared from N -protected a-annino dicarboxyhc acids and paraformaldehyde, are employed for dual protection of the a-annino and a-carboxy groups in the synthesis of P-aspartyl and y-glutamyl esters (Scheme 4).Py For this purpose the oxazolidinone derivatives are synthesized by treatment of the Z amino acids with paraformaldehyde in a nnixture of acetic anhydride, acetic acid, and traces of thionyl chloride or by azeotropic distillation of the Z amino acids with paraformaldehyde and 4-toluenesulfonic acid in benzene. The resulting heterocychc compounds are readily converted into the tert-butyl esters with isobutene under acid catalysis. Esterification is achieved with tert-butyl bromidet or with Boc-F.P l Finally, the oxazolidinone ring is opened by alkaline hydrolysis or catalytic hydrogenolysis to yield the tert-butyl esters. [Pg.244]

Chalcones undergo a similar type of reaction.Various oxazolidine derivatives can be prepared from carbodiimide and oxiranes with HBF4. ° Oxiranes are converted to oxazolidines by the most different reactants. Examples of such reactions are presented in Eqs. 206-210. Oxiranes react with Schiff bases to give 1,3-oxazines (Eq. 206). ° ... [Pg.93]


See other pages where Oxazolidines, preparation from is mentioned: [Pg.242]    [Pg.290]    [Pg.111]    [Pg.254]    [Pg.242]    [Pg.290]    [Pg.111]    [Pg.254]    [Pg.300]    [Pg.216]    [Pg.167]    [Pg.281]    [Pg.290]    [Pg.291]    [Pg.151]    [Pg.155]    [Pg.118]    [Pg.46]    [Pg.325]    [Pg.163]    [Pg.590]    [Pg.590]    [Pg.300]    [Pg.4]    [Pg.267]    [Pg.86]   


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