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Addition Michael-type

Conjugate addition readily occurs onto 4-substituted methylenepyrazol-3-ones [Pg.105]


Conventional synthetic schemes to produce 1,6-disubstituted products, e.g. reaction of a - with d -synthons, are largely unsuccessful. An exception is the following reaction, which provides a useful alternative when Michael type additions fail, e. g., at angular or other tertiary carbon atoms. In such cases the addition of allylsilanes catalyzed by titanium tetrachloride, the Sakurai reaction, is most appropriate (A. Hosomi, 1977). Isomerization of the double bond with bis(benzonitrile-N)dichloropalladium gives the y-double bond in excellent yield. Subsequent ozonolysis provides a pathway to 1,4-dicarbonyl compounds. Thus 1,6-, 1,5- and 1,4-difunctional compounds are accessible by this reaction. [Pg.90]

In the reaction of Q,/3-unsaturated ketones and esters, sometimes simple Michael-type addition (insertion and hydrogenolysis, or hydroarylation, and hydroalkenylation) of alkenes is observed[53,54]. For example, a simple addition product 56 to methyl vinyl ketone was obtained by the reaction of the heteroaromatic iodide 55[S5]. The corresponding bromide affords the usual insertion-elimination product. Saturated ketones are obtained cleanly by hydroarylation of o,/3l-unsaturated ketones with aryl halides in the presence of sodium formate, which hydrogenolyses the R—Pd—I intermediate to R— Pd—H[56]. Intramolecular hydroarylation is a useful reaction. The diiodide 57 reacts smoothly with sodium formate to give a model compound for the afla-toxin 58. (see Section 1.1.6)[57]. Use of triethylammonium formate and BU4NCI gives better results. [Pg.136]

Other reactions that show preference for the acidic N-3—H group include Mannich aminomethylation by treatment with formaldehyde and an amine (38) to yield compound (8), reaction with ethyleneimine (39) to give (9), and Michael-type additions (40) such as the one with acrylonitrile to give (10) ... [Pg.251]

This Michael-type addition is catalyzed by lanthanum(3+) [16096-89-2] (80). Ethylene glycol [107-21-1] reacts with maleate under similar conditions (81). A wide range of nucleophilic reagents add to the maleate and fumarate frameworks including alcohols, ammonia, amines, sulfinic acids, thioureas, Grignard reagents, Michael reagents, and alkali cyanides (25). [Pg.452]

Thiols can be prepared by a variety of methods. The most-utilised of these synthetic methods for tertiary and secondary thiols is acid-catalysed synthesis for normal and secondary thiols, the most-utilised methods are free-radical-initiated, alcohol substitution, or halide substitution for mercaptoalcohols, the most-utilised method is oxhane addition and for mercaptoacids and mercaptonitnles, the most-utilised methods are Michael-type additions. [Pg.10]

Michael-Type Additions. Michael additions are generally used to prepare methyl 3-mercaptopropionate (eq. 10) and mercaptopropionitrile (eq. 11) by the reaction of methyl acrylate or acrylonitrile and hydrogen sulfide using a basic catalyst. This reaction proceeds as shown ... [Pg.11]

Class (2) reactions are performed in the presence of dilute to concentrated aqueous sodium hydroxide, powdered potassium hydroxide, or, at elevated temperatures, soHd potassium carbonate, depending on the acidity of the substrate. Alkylations are possible in the presence of concentrated NaOH and a PT catalyst for substrates with conventional pX values up to - 23. This includes many C—H acidic compounds such as fiuorene, phenylacetylene, simple ketones, phenylacetonittile. Furthermore, alkylations of N—H, O—H, S—H, and P—H bonds, and ambident anions are weU known. Other basic phase-transfer reactions are hydrolyses, saponifications, isomerizations, H/D exchange, Michael-type additions, aldol, Darzens, and similar... [Pg.186]

The Michael-type addition of maleic hydrazide and other pyridazinones to activated alkenes, such as methyl acrylate, acrylonitrile, methyl vinyl ketone and other a,/3-unsatu-rated carbonyl compounds, results in the formation of mono-lV-substituted products. [Pg.15]

Michael-type addition, hydroxymethylation and Mannich reaction take place at nitrogen to give the corresponding 2-substituted 4-hydroxyphthalazin-l(2/f)-ones. [Pg.17]

The use of carbon nucleophiles in Michael-type addition reactions with pteridine and its derivatives leads to a quite complicated and divergent pattern. These reactions are strongly dependent on the nature of the carbon nucleophile and can be divided into various categories. [Pg.288]

The reactions of pyrroles with dienophiles generally follow two different pathways involving either a [4 + 2] cycloaddition or a Michael-type addition to a free a-position of the pyrrole ring. Pyrrole itself gives a complex mixture of products with maleic anhydride or maleic acid and with benzyne reacts to give 2-phenylpyrrole rather than a product of cycloaddition (Scheme 47). [Pg.65]

Aziridines have been prepared stereospecifically by the nucleophilic addition of the nitrogen residue to alkenes <80T73). Introduction of the nitrene is accomplished readily via a Michael-type addition with free diphenylsulfilimine (Scheme 12), and where a chiral sulfilimine is used the chirality is transferred to the aziridine with optical yields in excess of 25%. [Pg.87]

Indolo[2,3-d][l,3]thiazine-2,4-dithione formation, 4, 299 Indolothiazines synthesis, 4, 519 Indoloyl azides Curtius rearrangement, 4, 288 Indolyl anions acylation, 4, 232 alkylation, 4, 235 Michael-type additions, 4, 236 Indomethacin... [Pg.674]

In contrast, tertiary amines do not possess a proton to transfer, and the reaction of the Michael-type addition adduct with ECA can only initiate polymerization to form high molecular weight adhesive polymer, as shown earlier in Scheme 1. [Pg.863]

When having an Q ,/3-unsaturated carbonyl moiety, 2(5/7)-furanones are capable of undergoing 1,4-Michael-type additions. It was found that 1,4-addition reactions of thiophenols to the furanones 168,170, and 172 take place at room temperature in the presence of triethylamine to give a quantitative yield of the adducts 169, 171, and 173. Complete diastereoselective Michael-type addition occurred in all cases (Scheme 48) (88T7213). [Pg.137]

Finally, obtaining olefin 93 from the reaction of thiirene oxide 18a with two equivalents of phenylmagnesium bromide may be a consequence of the initial nucleophilic Michael-type addition of the latter across the carbon carbon double bond of the cyclic sulfone22 (see equation 31). [Pg.411]

Base-induced eliminative ring fission, in which both the double bond and the sulfone function take part, has been observed in thiete dioxides253. The reaction can be rationalized in terms of initial Michael-type addition to the double bond of the ring vinyl sulfone, followed by a reverse aldol condensation with ring opening. The isolation of the ether 270c in the treatment of 6c with potassium ethoxide (since the transformation 267 -> 268 is not possible in this case) is in agreement with the reaction mechanism outlined in equation 101253. [Pg.455]

Scheme 4 Access to various a,/ -unsaturated carbene complexes from alkynylcarbene complexes 23. A 1,3-Dipolar cycloaddition. B Diels-Alder reaction. C Ene reaction. D [2+2] Cycloaddition. E Michael-type addition followed by cyclization. F Michael-type additions... Scheme 4 Access to various a,/ -unsaturated carbene complexes from alkynylcarbene complexes 23. A 1,3-Dipolar cycloaddition. B Diels-Alder reaction. C Ene reaction. D [2+2] Cycloaddition. E Michael-type addition followed by cyclization. F Michael-type additions...
In the presence of a catalytic amount of triethylamine, a readily enolizable carbonyl compound like acetylacetone (25) can undergo a Michael-type addition onto the triple bond of 23 with C-C bond formation, and subsequent 1,2-addition of the hydroxy group with elimination of an alcohol (MeOH or EtOH) to eventually yield a pyranylidene complex 28 (mode E) [29]. The most versatile access to / -donor-substituted ethenylcarbene complexes 27 is by Michael-type additions of nucleophiles, including alcohols [30-32], primary... [Pg.25]

Scheme 5 Access to / -amino-substituted a,/ -unsaturated Fischer carbene complexes 30 by Michael-type addition of amines to alkynylcarbene complexes 23 (R=Et) [30,33]... Scheme 5 Access to / -amino-substituted a,/ -unsaturated Fischer carbene complexes 30 by Michael-type addition of amines to alkynylcarbene complexes 23 (R=Et) [30,33]...
With any substrate, when Y is an ion of the type Z—CR2 (Z is as defined above R may be alkyl, aryl, hydrogen, or another Z), the reaction is called the Michael reaction (see 15-21). In this book, we will call all other reactions that follow this mechanism Michael-type additions. Systems of the type C=C—C=C—Z can give 1,2, 1,4, or 1,6 addition. Michael-type reactions are reversible, and compounds of the type YCH2CH2Z can often be decomposed to YH and CH2=CHZ by heating, either with or without alkali. [Pg.976]

For nucleophilic addition the direction of attack has been studied very little, except for Michael-type addition, with compounds of the type C—C—Z. Here the negative part of the reagent almost always attacks regioselectively at the carbon that does not carry the Z (see p. 976). [Pg.985]

In certain cases, Michael reactions can take place under acidic conditions. Michael-type addition of radicals to conjugated carbonyl compounds is also known.Radical addition can be catalyzed by Yb(OTf)3, but radicals add under standard conditions as well, even intramolecularly. Electrochemical-initiated Michael additions are known, and aryl halides add in the presence of NiBr2. Michael reactions are sometimes applied to substrates of the type C=C—Z, where the co-products are conjugated systems of the type C=C—Indeed, because of the greater susceptibility of triple bonds to nucleophilic attack, it is even possible for nonactivated alkynes (e.g., acetylene), to be substrates in this... [Pg.1024]


See other pages where Addition Michael-type is mentioned: [Pg.316]    [Pg.57]    [Pg.135]    [Pg.356]    [Pg.303]    [Pg.575]    [Pg.678]    [Pg.700]    [Pg.703]    [Pg.824]    [Pg.944]    [Pg.125]    [Pg.127]    [Pg.96]    [Pg.674]    [Pg.693]    [Pg.36]    [Pg.76]    [Pg.105]    [Pg.152]    [Pg.404]    [Pg.1014]    [Pg.1310]    [Pg.21]   
See also in sourсe #XX -- [ Pg.45 ]

See also in sourсe #XX -- [ Pg.225 , Pg.313 , Pg.314 ]




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