CYCLIC KETONES FROM

Preparation of spirooxaziridines from cyclic ketones poses no problems nor does oxaziridine synthesis from cyclic Schiff bases, which was preferably carried out with pyrro-lines to give, for example (245) (59JCS2102) and, in connection with tranquilizer synthesis, with heterocyclic seven-membered rings to give, for example, (246) (63JOC2459). [Pg.228]

The enamines derived from cyclic ketones give the normal alkylated products, although there is some evidence that unstable cycloadducts are initially formed (55b). Thus the enamine (28) derived from cyclohexanone and pyrrolidine on reaction with acrylonitrile, acrylate esters, or phenyl vinyl sulfone gave the 2-alkylated cyclohexanones (63) on hydrolysis of the intermediates (31,32,55,56). These additions are sensitive to the polarity of the solvent. Thus (28) in benzene or dioxane gave an 80% yield of the... [Pg.127]

Enamines from cyclic ketones give derivatives of triazole 133,134). The enamine (113) reacts with p-nitrophenyl azide to give the triazoline (194), which on treatment with acid gives the triazole (195). [Pg.160]

While most acylation and benzoylation studies have involved enamines derived from cyclic ketones, extensions to aldehyde derived enamines have also been successful (400). [Pg.389]

The acylation of enamines derived from cyclic ketones, which can lead to the acyl ketone or ring expansion (692-694), was studied by NMR and mass spectroscopic analysis of the products (695,696). In a comparative study of the rates of diphenylketene addition to olefins, a pronounced activation was observed in enamines (697). Enamine N- and C-acylation products were obtained from reactions of Schiff s bases (698), vinylogous urethanes (699), cyanamides (699), amides (670,700), and 2-benzylidene-3-methylbenzothiazoline (672) with acid chlorides, anhydrides, and dithio-esters (699). [Pg.392]

Eu(fod)3 and SnCU-catalyzed heterocycloadditions of o-silylenol ethers deriving from cyclic ketones [113]... [Pg.136]

The enolates derived from cyclic ketones are necessarily /(-isomers. The enolate of cyclohexanone reacts with benzaldehyde to give both possible stereoisomeric products. The stereoselectivity is about 5 1 in favor of the anti isomer under optimum... [Pg.69]

Table 4.1. Rate Data for the Formation of Alkenals from Cyclic Ketones by Type I...

Cyclic nitroalkenes are prepared from cyclic ketones via nitration of vinylstannanes with tetranitromethane in DMSO, as shown in Eq. 2.36, where DMSO is a critical choice of solvent for replacing tin by nitro at the unsaturated carbon. The conversion of ketones to vinylstannanes... [Pg.14]

Enantioselective alkylation of ketones. Chiral imines prepared from cyclic ketones and 1 on metalation and alkylation are converted to chiral 2-alkyleyclo-alkanones in 87-100% enantiomeric purity.1 The high cnantioselectivity is dependent on chelation of the lithium ion in the anion by the methoxyl group, which results in a rigid structure. [Pg.11]

Enamine (235) obtained from cyclic ketones and the acetal of /V-methyl-2-pyrrolidone gave a fused 2-pyrone [83IJC(B)1083]. 2//-Chromenes were obtained from of 3,5-dichlorosalicylaldehyde and enamines (94RRC183) (Scheme 42). The pyran ring is formed by a reaction of aminals of conjugated w-dimethylaminoaldehydes with cyclic /1-dicarbonyl compounds (94IZV285) (Scheme 43). [Pg.333]

The chemical properties of cyclic ketones also vary with ring size. Lower members (addition reactions, than corresponding acyclic ketones. The Cg—C12 ketones are unreactive, reflecting the strain and high enol content of medium-sized ring systems. Lactones are prepared from cyclic ketones by the Bayer-Villiger oxidation reaction with peracids. S-Caprolactone is manufactured from cyclohexane by this process ... [Pg.500]

The use of a-thiophenyl enones (106 Scheme 12) allows the preparation of phenols such as (107) from cyclic ketones (18).30 The same product can also be obtained by normal Robinson annulation of methyl vinyl ketone (30) and the p-keto sulfoxide (lOS).30 Acceptors other than a, 3-unsaturated carbonyls have been used in both the Michael reaction and the Robinson annulation process. For example, nu-... [Pg.8]

Table III. Acid Yields from Cyclic Ketones...

Homer-Wadsworth-Emmons reactions of ketones and aldehydes with phosphono-acetate esters, (R20)2P(=0)CH2C02R1, produce E/Z mixtures of a, /Tunsaturated esters. Use of the conventional reagent, sodium hydride, gives some selectivity. The combination of tin(II) triflate and A -cthylpipcndine enhances—and sometimes also reverses—the selectivity in most cases studied.71 Six-membered oxo-coordinated tin intermediates are proposed to control the selectivities observed. A similarly selective synthesis of trisubstituted exocyclic alkenes from cyclic ketones has been reported.72... [Pg.13]

A brief review of procedures for asymmetric metal-catalyzed Baeyer-Villiger oxidations is given with asymmetric copper-catalyzed synthesis of 3-phenyl-2-oxepanone as representative of the enantioselective synthesis of lactones from cyclic ketones . [Pg.69]

PdCl2(PhCN)2-catalysed Claisen rearrangement of the allyl vinyl ether 474 derived from cyclic ketone at room temperature affords the syn product 475 with high diastereoselectivity [203]. In contrast to thermal Claisen rearrangement, the Pd(II)-catalysed Claisen rearrangement is always stereoselective, irrespective of the geometry of allylic alkenes. The anti product is obtained by the thermal rearrangement in the presence of 2,6-dimethylphenol at 100 °C for lOh. [Pg.159]

Thermal reactions of 1,2,3-selenadiazoles synthesized from cyclic ketones 121 with an excess amount (200equiv)... [Pg.542]

Substitution of the acetate group at the C-3 position of the /3-sultam 105 can occur by reaction with silyl enol ethers in the presence of zinc iodide or zinc chloride. When the diazo compound is used, after desilylation with tetrabutyl-ammonium fluoride (TBAF), photochemical cyclization gives the bicyclic /3-sultam 106 as a mixture of two cis/ fra -diastereoisomers. When silyl enol ethers derived from cyclic ketones are used, the substitution product is stabilized by a retro-Michael-type reaction leading to open-chained sulfonamides 107 (Scheme 31) <1997LA1261>. [Pg.741]

Independently, Yamamoto, Yanagisawa, and others reported the asymmetric aldol reaction using trimethoxysilyl enol ethers.19 The reaction was conducted with aldehydes and trimethoxysilyl enol ethers in the presence of Tol-BINAP-AgF to give the corresponding adducts with high enantioselectivities and diastereoselectiv-ities. They obtained vyra-aldol adducts as major products even when silyl enol ethers derived from cyclic ketones were used. Moreover, when a,(3-unsaturated aldehydes were employed as substrates, 1,2 adducts were obtained exclusively (Table 9.10). From an NMR study and correlation between the E Z ratio of the enol ethers and diastereoselectiviy, they proposed a cyclic transition state (Fig. 9.5). Thus, the reaction of E enol ethers proceeded via a boat form, whereas the reaction of Z enol ethers took place via a chair form. [Pg.273]

The regioselective attack of nonactivated C-H-bonds by an excited carbonyl group is demonstrated with the transannular cyclization of bicyclic diketones 76, which can easily be prepared from cyclic ketones 75 according to Stetter et al. [61]. Upon irradiation, the selectively excited benzoyl... [Pg.68]

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