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Alkenes, trisubstituted

Trisubstituted alkenes are usually poor substrates for Heck chemistry, and must almost always be used in an intramolecular way. Treatment of the phenolic ether 5.177 with a palladium catalyst resulted in oxidative addition and insertion, leading to a stable ti -intermediate 5.179 as it has no available p-hydrogen [Pg.171]


Many examples of insertions of internal alkynes are known. Internal alkynes react with aryl halides in the presence of formate to afford the trisubstituted alkenes[271,272]. In the reaction of the terminal alkyne 388 with two molecules of iodobenzene. the first step is the formation of the phenylacetylene 389. Then the internal alkyne bond, thus produced, inserts into the phenyl-Pd bond to give 390. Finally, hydrogenolysis with formic acid yields the trisubstituted alkene 391(273,274], This sequence of reactions is a good preparative method for trisubstituted alkenes from terminal alkynes. [Pg.181]

Allylation of the 10-carborane 236 (pKa = 18-22) with diallyl carbonate is possible under neutral conditions to give 237[146], Allylation and rearrangement of the trialkylalkynylborane 238 affords the trisubstituted alkene 239 stereoselectively [ 147],... [Pg.322]

Trisubstituted alkene (Section 5 6) Alkene of the type R2C=CHR in which there are three carbons directly bonded to the carbons of the double bond (The R groups may be the same or different)... [Pg.1296]

Mono-, di-, and trialkylboranes may be obtained from olefins and the trifunctional borane molecule. Simple unhindered alkenes yield trialkylboranes and it is not possible to halt the reaction at the mono- or dialkylborane stage. With more hindered and trisubstituted alkenes the reaction can be controlled to stop at the dialkylborane stage. [Pg.308]

Tetrasubstituted and some hindered trisubstituted alkenes react rapidly only to the monoalkylborane stage. Rarely, when the tetrasubstituted double bond is incorporated in a cycHc stmcture, does hydroboration under normal conditions fail (25—27). However, such double bonds may react under conditions of greater force (25,28—31). Generally, trialkylboranes are stable at normal temperatures, undergoing thermal dissociation at temperatures above 100°C (32—34). In the presence of B—H bonds, trialkylboranes undergo a redistribution reaction (35—38). [Pg.308]

For a review of synthetic methods applicable to trisubstituted alkenes see J. Faulkner, Synthe.ais, 175 (1971). [Pg.30]

Raney Nickel W2 or W4, EtOH, 85-100% yield. Mono- and dimethoxy-substituted benzyl ethers and benzaldehyde acetals are not cleaved under these conditions, and trisubstituted alkenes are not reduced. [Pg.80]

What stereochemistry do you expect for the trisubstituted alkene obtained by E2 elimination of the following alkyl halide on treatment with KOE1 (Reddish brown - Br.)... [Pg.389]

The Wittig reaction is extremely general, and a great many monosubstituted, disubstituted, and trisubstituted alkenes can be prepared from the appropriate... [Pg.721]

The Arrhenius frequency factors [log(T/M V)] for addition of carbon centered radicals to the unsubstiUited terminus of monosubslituted or 1,1-disubstituted olefins cover a limited range (6.0-9.0), depend primarily on the steric demand of the attacking radical and are generally unaffected by remote alkene substituents. Typical values of log(T/M" V) are ca 6.5 for tertiary polymeric (e.g. PMMA ), ca 7.0 for secondary polymeric (PS, PMA, and ca 7.5, 8.0 and 8.5 for small tertiary (e.g. /-C4H9 ), secondary (i-CiH ) and primary (CHj, CbHs ) radicals respectively (Section 4.5.4).4 For 1,2,2-trisubstituted alkenes the frequency factors arc about an order of magnitude lower.4 The trend in values is consistent with expectation based on Iheoretical calculations. [Pg.24]

Ketosilanes react with alkyl lithiums in a diastereoselective manner (7), the preferred diastereoisomer being the one predicted on the basis of Cram s Rule acidic or basic treatment provides a stereoselective route to trisubstituted alkenes. [Pg.128]

Of greater potential practical significance, however, are the note193 and full papers194,195 in which Fabre, Julia and Verpeaux describe a new stereoselective synthesis of trisubstituted alkenes in which vinyl sulphones are attacked by Grignard reagents in the presence of iron or nickel catalysts (equations 82-84). [Pg.958]

Alkenes have also been converted to more highly oxidized products. Examples are (1) Treatment with KMn04 in aqueous acetone containing acetic acid gives a-hydroxy ketones. (2) 1,2-Disubstituted and trisubstituted alkenes give a-chloro ketones when oxidized with chromyl chloride in acetone RCH=CR R"—> RCOCCIR R". (3) a-Iodo ketones can be prepared by treating alkenes with... [Pg.1538]

Only c/s-disubstituted and trisubstituted alkenes yield l,4-dioxan-2-ones by way of a cycloaddition reaction when oxidised by dimethyl a-peroxy lactone. An open 1,6-dipolar intermediate is postulated, involving steieoelectronic control <96JA4778>. [Pg.306]

Based on information accrued during the stereochemical elucidation, macrolactone 85 was identified as a viable synthetic intermediate (Scheme 12). The authors were cognizant of the potential challenges that could arise. First, the required formation of a trisubstituted alkene in a projected Horner-Emmons macrocyclization was without strong precedent. Also, this strategy would necessitate a stereoselective reduction of the Cl5 ketone, which was predicted to be feasible based on MM2 calculations. [Pg.66]

It might seem that allylic functionalisation can be used only on terminal alkenes such as (26) or trisubstituted alkenes, such as (31) when the orientation of addition is unambiguous. [Pg.311]

A mild, Fe(CO)5-catalyzed isomerization of this type was reported by Gree and coworkers [173]. Allylic alcohols having mono-, di-, trisubstituted alkene are readily converted into their corresponding ketones, whereas polyunsaturated derivatives do not rearrange (Scheme 54). [Pg.63]

Stereoselective syntheses of trisubstituted alkenes are based on E- and Z-alkenyldioxaborinanes. Reaction with an alkyllithium reagent forms an ate adduct that rearranges on treatment with iodine in methanol.31... [Pg.796]

A number of chiral ketones have been developed that are capable of enantiose-lective epoxidation via dioxirane intermediates.104 Scheme 12.13 shows the structures of some chiral ketones that have been used as catalysts for enantioselective epoxidation. The BINAP-derived ketone shown in Entry 1, as well as its halogenated derivatives, have shown good enantioselectivity toward di- and trisubstituted alkenes. [Pg.1102]

Trisubstituted alkenes are oxidized selectively at the more-substituted end of the carbon-carbon double bond, indicating that the ene reaction step is electrophilic in character. [Pg.1125]

Double bonds tend to migrate to more highly substituted positions within a substrate that is, terminal alkenes isomerize to disubstituted or trisubstituted alkenes, disubstituted alkenes tend to migrate to trisubstituted, and trisubstituted to tetrasubstituted alkenes. Of course, migration can go both ways, and adsorbed surface species may not exhibit the same thermodynamic stability as their desorbed relatives. (The rate of migration is strongly catalyst dependent for example, it frequently occurs rapidly on Pd and slowly on Pt.)... [Pg.292]

The interest in catalyst recyclability has led to the development of biphasic catalysts for hydro-boration.22 Derivitization of Wilkinson s catalyst with fluorocarbon ponytails affords [Rh(P (CH2)2(CF2)5CF3 3)3Cl] which catalyzes FIBcat addition to norbornene in a mixture of C6FnCF3 and tetrahydrofuran (TF1F) or toluene (alternatively a nonsolvent system can be used with just the fluorocarbon and norbornene) to give exo-norborneol in 76% yield with a turnover number up to 8,500 (Scheme 4). Mono-, di- and trisubstituted alkenes can all be reacted under these conditions. The catalyst can be readily recycled over three runs with no loss of activity.23... [Pg.268]

An interesting feature of the cyclization of y, -unsaturated alcohols is the marked effect on product isomer distribution by the nature of substituents remote from the double bond (cf. 42 and Scheme 59).98 Complete stereospecificity is observed for the phenyl derivative 42a in contrast to 42b and c, and the isomer ratio is reversed for 42d. The suggested mechanism98 is shown in Scheme 60 the trisubstituted alkene (45) is mainly converted into a pyran (46) rather than a tetrahydrofuran derivative (Scheme 61). [Pg.347]

Trisubstituted Alkenes. With very few exceptions, trisubstituted alkenes that are exposed to Brpnsted acids and organosilicon hydrides rapidly undergo ionic hydrogenations to give reduced products in high yields. This is best illustrated by the broad variety of reaction conditions under which the benchmark compound 1-methylcyclohexene is reduced to methylcyclohexane.134 146,192 202 203 207-210 214 234 When 1-methylcyclohexene is reduced with one equivalent of deuterated triethylsilane and two equivalents of trifluoroacetic acid at 50°, methylcyclohexane-... [Pg.38]

Exceptions to the generally facile ionic hydrogenation of trisubstituted alkenes include the resistance of both 2-methyl-1-nitropropene (R = NO2) and 3,3-dimeth-ylacrylic acid (R = CO2H) to the action of a mixture of triethylsilane and excess trifluoroacetic acid at 50° (Eq. 85).234 The failure to undergo reduction is clearly related to the unfavorable effects caused by the electron-withdrawing substituents on the energies of the required carbocation intermediates. [Pg.40]


See other pages where Alkenes, trisubstituted is mentioned: [Pg.221]    [Pg.313]    [Pg.323]    [Pg.323]    [Pg.198]    [Pg.221]    [Pg.194]    [Pg.316]    [Pg.168]    [Pg.112]    [Pg.922]    [Pg.1015]    [Pg.1425]    [Pg.46]    [Pg.958]    [Pg.16]    [Pg.1079]    [Pg.1103]    [Pg.150]    [Pg.240]    [Pg.286]    [Pg.94]    [Pg.96]    [Pg.326]   
See also in sourсe #XX -- [ Pg.227 ]

See also in sourсe #XX -- [ Pg.53 ]

See also in sourсe #XX -- [ Pg.214 , Pg.380 ]

See also in sourсe #XX -- [ Pg.133 ]

See also in sourсe #XX -- [ Pg.301 ]




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Alkene, -trisubstituted, formation

Alkenes trisubstituted alkene reduction

Alkenes, (£>selective synthesis trisubstituted

Alkenes, trisubstituted Julia coupling

Alkenes, trisubstituted synthesis

Alkenes, trisubstituted via tandem vicinal difunctionalization

Heck coupling reactions trisubstituted alkenes

Intrazeolite photooxygenation trisubstituted alkene regioselectivity

Regioselectivity dimethyl trisubstituted alkenes

Regioselectivity trisubstituted alkenes

Site selectivity trisubstituted alkenes

Synthesis of Trisubstituted Alkenes

Trisubstituted alkene epoxidation

Trisubstituted alkenes asymmetric epoxidation

Trisubstituted alkenes chloride

Trisubstituted alkenes intrazeolite photooxygenation

Trisubstituted alkenes structures

Trisubstituted gem-dimethyl alkene

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