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Allyl silanes reactions

Now a Lewis-acid-catalysed reaction of the allyl silane via a p-silyl cation, gives the lactone. The This silicon chemistry was double bond in these exo-methylene lactones easily moves into the ring in acid or base so the mild devised by A. Haider, Synthesis, conditions for allyl silane reactions are ideal. 19S5, 271. [Pg.445]

Reactions alkylations, reactions with epoxides and aldehydes, conjugate additions Heterocyclic synthesis with allyl silanes Reactions with Co-stabilised cations An Allyl Dianion The Role of Tin in Anion Formation Halide Exchange with Chelation Indium Allyls Allyl Anions by Deprotonation The synthesis ofall-trans dienes The synthesis ofall-trans retinol... [Pg.173]

The titanium(IV) chloride catalyzed addition of allylic silanes to (E)-(2-nitroethenyl)benzene affords y,<5-unsaturated nitronates which, on treatment with low valent titanium species [generated in situ from titanium(IV) and zinc], give y,<5-unsaturated nitriles. For example, [(Zs)-2-butenyl]-(dimethyl)phenylsilane underwent reaction with ( )-(2-nitroethenyl)benzene to give 3-methyl-2-phenyl-4-pentenenitrile in 65 % yield as a 3 1 mixture of diastereomers of unassigned configuration22. [Pg.1019]

Allyl silanes react with epoxides, in the presence of Bp3-OEt2 to give 2-allyl alcohols. The reaction of a-bromo lactones and CH2=CHCH2Si SiMe3)3 and AIBN leads to the a-allyl lactone. " Benzyl silanes coupled with allyl silanes to give ArCH2—R derivatives in the presence of VO(OEt)Cl2 " and allyltin compounds couple with allyl silanes in the presence of SnCU. " Allyl silanes couple to the a-carbon of amines under photolysis conditions. ... [Pg.535]

Allylic silanes react with aldehydes, in the presence of Lewis acids, to give an allyl-substituted alcohol. In the case of benzylic silanes, this addition reaction has been induced with Mg(C104)2 under photochemical conditions. The addition of chiral additives leads to the alcohol with good asymmetric induction. In a related reaction, allylic silanes react with acyl halides to produce the corresponding carbonyl derivative. The reaction of phenyl chloroformate, trimethylallylsilane, and AICI3, for example, gave phenyl but-3-enoate. ... [Pg.1239]

Allylic silanes and stannanes react with various electrophiles with demetallation. These reactions can occur via several related mechanisms. Both types of reactants can deliver alkylic groups to electrophilic centers such as carbonyl and iminium. [Pg.784]

Most reactions of alkenyl and allylic silanes require strong carbon electrophiles and Lewis acid catalysts are often involved. The most useful electrophiles from a synthetic standpoint are carbonyl compounds, iminium ions, and electrophilic alkenes. [Pg.815]

There are also some reactions of allylic silanes that proceed through anionic silicate species. These reactions usually involve activation by fluoride and result in transfer of an allylic anion. [Pg.815]

Trichloro- and trifluorosilanes introduce another dimension into the reactivity of allylic silanes. The silicon in these compounds is electrophilic and can expand to pentaco-ordinate and hexacoordinate structures. These reactions can occur through a cyclic or chelated TS. [Pg.815]

A variety of electrophilic catalysts promote the addition of allylic silanes to carbonyl compounds.86 The original catalysts included typical Lewis acids such as TiCl4 or BFj.87 This reaction is often referred to as the Sakurai reaction. [Pg.815]

Although the allylation reaction is formally analogous to the addition of allylic boranes to carbonyl derivatives, it does not normally occur through a cyclic TS. This is because, in contrast to the boranes, the silicon in allylic silanes has little Lewis acid character and does not coordinate at the carbonyl oxygen. The stereochemistry of addition of allylic silanes to carbonyl compounds is consistent with an acyclic TS. The -stereoisomer of 2-butenyl(trimethyl)silane gives nearly exclusively the product in... [Pg.816]

Intramolecular reactions can also occur between carbonyl groups and allylic silanes. These reactions frequently show good stereoselectivity. For example, 7 cyclizes primarily to 8 with 4% of 9 as a by-product. The two other possible stereoisomers are not observed.98 The stereoselectivity is attributed to a preference for TS 7A over TS 7B. These are both synclinal structures but differ stereoelectronically. In 7A, the electron flow is approximately anti parallel, whereas in 7B it is skewed. It was suggested that this difference may be the origin of the stereoselectivity. [Pg.819]

Reaction of allylic silanes with enantiomerically pure 1,3-dioxanes has been found to proceed with moderate enantioselectivity.104 The homoallylic alcohol can be liberated by oxidation followed by base-catalyzed (3-elimination. The alcohols obtained in this way are formed in 70 5% e.e. [Pg.820]

While trifluoro and other halosilanes function by increased electrophilicity at silicon, nucleophilic reactivity of allylic silanes can be enhanced by formation of anionic adducts (silicates). Reaction of allylic silanes with aldehydes and ketones can... [Pg.823]

Scheme 9.4. Reactions of Alkenyl and Allylic Silanes with Aldehydes, Ketones, Acetals,... Scheme 9.4. Reactions of Alkenyl and Allylic Silanes with Aldehydes, Ketones, Acetals,...
Entries 11 to 13 are examples of iminium ion and acyliminium ion reactions. Note that in Entries 11 and 12, vinyl, rather than allylic, silane moieties are involved. Entries 14 and 15 illustrate the synthesis of (3,-y-unsaturated ketones by acylation of allylic silanes. [Pg.830]

Some examples of conjugate addition reactions of allylic silanes are given in Scheme 9.5. Entries 1 to 3 illustrate the synthesis of several (3-allyl ketones. Note that Entry 2 involves the creation of a quaternary carbon. Entry 4 was used in the synthesis of a terpenoid ketone, (+)-nootkatone. Entry 5 illustrates fluoride-mediated addition using tetrabutylammonium fluoride. These conditions were found to be especially effective for unsaturated esters. In Entry 6, the addition is from the convex face of the ring system. Entry 7 illustrates a ring closure by intramolecular conjugate addition. [Pg.833]

Reactions proceeding through open TS In this group, exemplified by BF3-catalyzed additions of allylic silanes and stannanes, the degree of stereochemical control is variable and often moderate. The stereoselectivity depends on steric factors in the open TS and can differ significantly for the E- and Z-isomers of the allylic reactant. [Pg.852]

Each of the unsaturated cyclic amines shown below has been synthesized by reaction of an amino-substituted allylic silane under iminium ion cyclization conditions (CH2=0, TFA). By retrosynthetic analysis, identify the appropriate precursor for each cyclization. Suggest a method of synthesis of each of the required amines. [Pg.857]

There are, however, serious problems that must be overcome in the application of this reaction to synthesis. The product is a new carbocation that can react further. Repetitive addition to alkene molecules leads to polymerization. Indeed, this is the mechanism of acid-catalyzed polymerization of alkenes. There is also the possibility of rearrangement. A key requirement for adapting the reaction of carbocations with alkenes to the synthesis of small molecules is control of the reactivity of the newly formed carbocation intermediate. Synthetically useful carbocation-alkene reactions require a suitable termination step. We have already encountered one successful strategy in the reaction of alkenyl and allylic silanes and stannanes with electrophilic carbon (see Chapter 9). In those reactions, the silyl or stannyl substituent is eliminated and a stable alkene is formed. The increased reactivity of the silyl- and stannyl-substituted alkenes is also favorable to the synthetic utility of carbocation-alkene reactions because the reactants are more nucleophilic than the product alkenes. [Pg.862]

As the intermediate formed in a polyene cyclization is a carbocation, the isolated product is often found to be a mixture of closely related compounds resulting from competing modes of reaction. The products result from capture of the carbocation by solvent or other nucleophile or by deprotonation to form an alkene. Polyene cyclizations can be carried out on reactants that have structural features that facilitate transformation of the carbocation to a stable product. Allylic silanes, for example, are stabilized by desilylation.12... [Pg.865]

The incorporation of silyl substituents not only provides for specific reaction products but can also improve the effectiveness of polyene cyclization. For example, although cyclization of 2a gave a mixture containing at least 17 products, the allylic silane 2b gave a 79% yield of a 1 1 mixture of stereoisomers.13 This is presumably due to the enhanced reactivity and selectivity of the allylic silane. [Pg.865]

The stereochemistry was controlled by Lewis acid-induced addition of these allylic silanes to aldehydes. The reaction of the silane with O-protected (S)-3-hydroxy-2-methylpropanal provides 15. The silane reacted with the benzyl-protected analog to provide 16. [Pg.1239]

Nitrostyrene reacts with allylzinc reagents in dry DMF at room temperature to give the addition products in excellent yield (Eq. 4.80).102 The reaction of allyl tin compounds or allyl silanes with nitroalkenes requires the assistance of Lewis acids to give the addition products in good yield (Eq. 4.81).103... [Pg.97]

In another example, Hg(OTf)2 has been used for the stereoselective ring expansion of 116 to 117 with excellent stereospecificity for the (Z)-isomer (Equation (43)).156 Carbomercuration reactions have also been observed for derivatives such as 118, which possesses both an allylic silane as well as an alkynyl functionality. For 118, the reaction affords the 5-m -ring compound 119 as the (Z)-isomer. Formation of the (/. )-isomcr is disfavored because the bulk of the TMS group precludes an anti-attack (Equation (44)).157... [Pg.439]


See other pages where Allyl silanes reactions is mentioned: [Pg.222]    [Pg.355]    [Pg.396]    [Pg.330]    [Pg.101]    [Pg.103]    [Pg.535]    [Pg.535]    [Pg.1024]    [Pg.83]    [Pg.821]    [Pg.825]    [Pg.1209]    [Pg.1228]    [Pg.1243]    [Pg.1245]    [Pg.146]   


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Allyl silane

Allyl silanes

Allylic silane

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