Ketenes alkoxy

The oxidation of the cyclic enol ether 93 in MeOH affords the methyl ester 95 by hydrolysis of the ketene acetal 94 formed initially by regioselective attack of the methoxy group at the anomeric carbon, rather than the a-alkoxy ketone[35]. Similarly, the double bond of the furan part in khellin (96) is converted ino the ester 98 via the ketene acetal 97[l23],... 

This synthetic process is applicable to the preparation of other ketene acetal derivatives of /3-alkoxy alcohols. Examples include the ketene acetal derivatives of tetrahydrofurfuryl alcohol and l-methoxy-2-propanol.3 There are a number of advantages in its use, including a simple, time-saving procedure, readily available and inexpensive reagents, and good yields of ketene acetal obtained by a one-step method. 

The superior donor properties of amino groups over alkoxy substituents causes a higher electron density at the metal centre resulting in an increased M-CO bond strength in aminocarbene complexes. Therefore, the primary decarbo-nylation step requires harsher conditions moreover, the CO insertion generating the ketene intermediate cannot compete successfully with a direct electro-cyclisation of the alkyne insertion product, as shown in Scheme 9 for the formation of indenes. Due to that experience amino(aryl)carbene complexes are prone to undergo cyclopentannulation. If, however, the donor capacity of the aminocarbene ligand is reduced by N-acylation, benzannulation becomes feasible [22]. 

Merlic et al. were the first to predict that exposing a dienylcarbene complex 126 to photolysis would lead to an ort/zo-substituted phenolic product 129 [74a]. This photochemical benzannulation reaction, which provides products complementary to the classical para-substituted phenol as benzannulation product, can be applied to (alkoxy- and aminocarbene)pentacarbonyl complexes [74]. A mechanism proposed for this photochemical reaction is shown in Scheme 54. Photo activation promotes CO insertion resulting in the chromium ketene in-... 

Alkoxycarbene complexes with unsaturation in the alkyl side chain rather than the alkoxy chain underwent similar intramolecular photoreactions (Eqs. 10 and 11) [60]. Cyclopropyl carbene complexes underwent a facile vinyl-cyclopropane rearrangement, presumably from the metal-bound ketene intermediate (Eqs. 12 and 13) [61]. A cycloheptatriene carbene complex underwent a related [6+2] cycloaddition (Eq. 14) [62]. 

The dimerization of the parent ketene gives the P-lactone. One molecule of ketene reacts across the C=C bond as a donor and the other molecule reacts across the C=0 bond as an acceptor. This is similar to the concerted [2+2] cycloaddition reaction between bis(trifluoromethyl)ketene and ethyl vinyl ether to afford the oxetane (Scheme 26) [127], A lone pair on the carbonyl oxygen in the ketene molecule as a donor activates the C=C bond as the alkoxy group in vinyl ether. 

The stereoselectivity of silyl ketene acetal Claisen rearrangements can also be controlled by specific intramolecular interactions.246 The enolates of a-alkoxy esters adopt the Z-configuration because of chelation by the alkoxy substituent. 

The ft -hydroxy ester resulting from the reaction of the tert-butyldimethylsilyl ketene acetal of ethyl acetate with a lactone under acid conditions can be reduced to the /3-alkoxy ester.306 The overall yields are excellent (Eq. 149). 

Okamoto, Y., Azuhata, T., and Sakurai, H., Dialkyl 3-alkoxy-3-(trimethylsi-loxy)-2-propenephosphonate a one step preparation of (dialkoxyphosphi-nyljmethyl-substituted ketene alkyl trimethylsilyl acetal, Chem. Lett., 1265, 1981. 

Domino reactions increasingly gain importance in the search for new drugs. Especially appropriate is the use of multi-component reactions in solution combinatorial chemistry. In such a process described by Wessel et al.1231 an alkoxy-nitroenone 48 was treated with different anilines 49 to give ketene-NO-acetals which in the presence of aromatic aldehydes and TfOH are transformed into 50 (scheme 10). The substrate 48 is readily available by oxidation of the nitrosugar 47. 

Cycloaddition of ketenes to Cjq is expected to be difficult due to their electrophilic character. Nevertheless, the reaction of Cjq vhth some aryloxy- and alkoxy-ketenes led to the successful characterization of cycloaddition-products [356]. The reaction proceeds via a formal [2-1-2] cycloaddition, followed by enolization and acylation. Products 320 are stable and can be obtained in moderate yields (Scheme 4.64). 

Kuryla and Leis [125a] recently reported that ortho esters are readily produced by the slow addition of vinylidene chloride to a sodium j8-alkoxy-alcoholate, dissolved or suspended in a solvent. The reaction is exothermic and produces either the ketene acetal or the ortho ester derivative while sodium chloride precipitates (Eq. 38). 

Reaction of diazomethyl ketone with ketene acetals to form 2,2-di-alkoxy-l,2-dihydropyrans [178]. 

The carbenoid from Et2Zn/CH2I2 [17], particularly when generated in the presence of oxygen [18], is more reactive than the conventional Simmons-Smith reagents. The milder conditions required are suitable for the preparation of 1-[16, 19] or 2-alkoxy-l-siloxycyclopropanes [20], which are generally more sensitive than the parent alkyl substituted siloxycyclopropanes (Table 2). Cyclopropanation of silyl ketene acetals is not completely stereospecific, since isomerization of the double bond in the starting material competes with the cyclopropanation [19]. 

The application of chiral auxiliary groups which can be removed after the cycloaddition has met with limited success. The chiral auxiliary can be attached to either the ketene or alkene moiety. In a study of dichloroketene cycloadditions with a series of enol ethers 18, to which a chiral alkoxy group is attached, diastereoselectivities ranged from 55 to 90%,n with the choice of chiral auxiliary being crucial to obtaining the desired diastereoselectivity. 

Photolysis of pentacarbonylcarbenechromium complexes produce species that react as if they were ketenes. although no evidence for the generation of free ketenes has been observed. Indeed, photolysis of chromium (alkoxy) carbenes in the presence of a range of simple alkenes produced cyclobutanones 1 in good to very good yield.8,9... 

Aldol condensation of a-amino silyl ketene acetals (l).10 2-Dibenzylami-noketene trimethylsilyl acetals (1) react with aldehydes premixed with TiCl4 to give a-amino-p-hydroxy carboxylic esters (2) with moderate to high syn-selectivity. Surprisingly, TiCl4-catalyzed reaction of 1 with a chiral a-alkoxy aldehyde proceeds with low asymmetric induction. 

JACS 107 2192 (alkyl and vinyl ketene), 2194 (alkoxy ketene), 4339 (vinyl ketene) (1985) 110 649 (1988) (alkyl ketene)... 

Considerable use has also been made of allyl carbonates as substrates for the allylation of Pd enolates.9 The reaction of Pd° complexes with allyl enol carbonates119,120 proceeds by initial oxidative addition into the allylic C—O bond of the carbonate followed by decarboxylation, yielding an allylpalladium enolate, which subsequently produces Pd° and the allylated ketone (equation 22). In like fashion, except now in an intermolecular sense, allyl carbonates have been found to allylate enol silyl ethers (equation 23),121 enol acetates (with MeOSnBu3 as cocatalyst) (equation 24),122 ketene silyl acetals (equation 25)123 and anions a to nitro, cyano, sulfonyl and keto groups.115,124 In these cases, the alkoxy moiety liberated from the carbonate on decarboxylation serves as the key reagent in generating the Pd enolate. 

Acyl ketenes also react with a variety of dienophiles such as enol ethers to give the corresponding 2-alkoxy-2,3-dihydro-4-pyranones [147]. 

As we have mentioned above, ketene N9S- and N,0-acetals are the intermediates in the preparation of 1,1-enediamines from ketene dithioacetals and ketene acetals, respectively, and they can be isolated from the reactions5,51,52,72. Further substitution of the methylthio or the alkoxy groups by amines yields 1,1-enediamines. 

Ketene N, O-acetals are converted to 1,1-enediamines when reacted with amines. For example, compound 45 has been prepared by substitution of the methoxy with amine (equation 16)79. Symmetric 1,1-enediamines are obtained when both the alkoxy and the amino substituents are displaced by the amine employed81. In this way, the reaction between ketene N, O-acetals 50 and piperidine leads to 1,1-dipipefidinoethylene (35) (equation 17)81. Alternatively, 35 can be prepared from the reaction of piperidine with triethyl orthoacetate82,83 or with ethoxyacetylene84, reactions which probably proceed via a ketene TV, 0-acetal intermediate. 

J. 3-Alkoxy Pyrroles via Addition of Isocyanide (or Carbon Monoxide) and Fragmenation of Ketenimines (or Ketenes)... 

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