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With Carbonyl Compounds

The reactions of organolithium compounds with carbonyl compounds, including carbon dioxide, may be interpreted as follows ... [Pg.930]

Both aldehydes and ketones contain the carbonyl group, hence a general test for carbonyl compounds will Immediately characterise both classes of compounds. The preferred reagent is 2 4-dinilrophenylhydrazine, which gives sparingly soluble phenylhydrazones with carbonyl compounds ... [Pg.1060]

Although several experimental data concerning the functionalization of cumulenic anions are availab. a (for a review see Ref. 10) (Table I), it remains difficult to predict the compos tion of the product of a particular reaction on a rationalistic basis. Especially the outcome of reactions with carbonyl compounds seems to be... [Pg.28]

Primary and secondary amines also react with epoxides (or in situ produced episulfides )r aziridines)to /J-hydroxyamines (or /J-mercaptoamines or 1,2-diamines). The Michael type iddition of amines to activated C—C double bonds is also a useful synthetic reaction. Rnally unines react readily with. carbonyl compounds to form imines and enamines and with carbo-tylic acid chlorides or esters to give amides which can be reduced to amines with LiAlH (p. Ilf.). All these reactions are often applied in synthesis to produce polycyclic alkaloids with itrogen bridgeheads (J.W. Huffman, 1967) G. Stork, 1963 S.S. Klioze, 1975). [Pg.291]

Other interesting regioselective reactions are carried out within the synthesis of nitrofurantoin. Benzaidehyde semicarbazone substitutes chlorine in chloroacetic ester with the most nucleophilic hydrazone nitrogen atom. Transamidation of the ester occurs with the di-protic outer nitrogen atom. Only one nucleophilic nitrogen atom remains in the cyclization product and reacts exclusively with carbonyl compounds. [Pg.308]

Sodium borohydride and lithium aluminum hydride react with carbonyl compounds in much the same way that Grignard reagents do except that they function as hydride donors rather than as carbanion sources Figure 15 2 outlines the general mechanism for the sodium borohydride reduction of an aldehyde or ketone (R2C=0) Two points are especially important about this process... [Pg.629]

Acetylene is condensed with carbonyl compounds to give a wide variety of products, some of which are the substrates for the preparation of families of derivatives. The most commercially significant reaction is the condensation of acetylene with formaldehyde. The reaction does not proceed well with base catalysis which works well with other carbonyl compounds and it was discovered by Reppe (33) that acetylene under pressure (304 kPa (3 atm), or above) reacts smoothly with formaldehyde at 100°C in the presence of a copper acetyUde complex catalyst. The reaction can be controlled to give either propargyl alcohol or butynediol (see Acetylene-DERIVED chemicals). 2-Butyne-l,4-diol, its hydroxyethyl ethers, and propargyl alcohol are used as corrosion inhibitors. 2,3-Dibromo-2-butene-l,4-diol is used as a flame retardant in polyurethane and other polymer systems (see Bromine compounds Elame retardants). [Pg.393]

A small amount of acetylene is used in condensations with carbonyl compounds other than formaldehyde. The principal uses for the resulting acetylenic alcohols are as intermediates in the synthesis of vitamins (qv). [Pg.393]

Six-membered heterocycles with two heteroatoms are prepared by reaction of diketene with a substrate containing a C—O or C—N multiple bond. With carbonyl compounds diketene reacts in the presence of acids to give l,3-dioxin-4-ones. The best known is 2,2,6-trimethyl-4H-l,3-dioxin-4-one [5394-63-8] (15), the so-called diketene—acetone adduct, often used as a diketene replacement that is safer to handle and to transport, albeit somewhat less reactive than diketene itself (103,104), forming acetylketene upon heating. [Pg.478]

Reaction With Carbonyl Compounds. Primary and secondary nitroparaffins undergo aldol-type reactions with a variety of aldehydes and ketones to give nitro alcohols (11). Those derived from the lower nitroparaffins and formaldehyde are available commercially (see Nitro alcohols). Nitro alcohols can be reduced to the corresponding amino alcohols (see Alkanolamines). [Pg.100]

Phosphine oxides may be prepared by the acid-cataly2ed reaction of phosphine with carbonyl compounds such as ketones (94). [Pg.382]

PUtzing erReaction. Quinoline-4-carboxyhc acids are easily prepared by the condensation of isatin [91-56-5] (16) with carbonyl compounds (50). The products may be decarboxylated to the corresponding quinolines. The reaction of isatin with cycHc ketones has been reported, eg, the addition of cyclohexanone gives the tricycHc intermediate (17) [38186-54-8] which upon oxidation produces quinoline-2,3,4-tricarboxyhc acid [16880-83-4] (51). [Pg.391]

PlCtet-SpenglerSynthesis. An acidic catalyst results in the condensation of P-pbenetbylamines with carbonyl compounds to give... [Pg.396]

A-Substituted pyrroles, furans and dialkylthiophenes undergo photosensitized [2 + 2] cycloaddition reactions with carbonyl compounds to give oxetanes. This is illustrated by the addition of furan and benzophenone to give the oxetane (138). The photochemical reaction of pyrroles with aliphatic aldehydes and ketones results in the regiospecific formation of 3-(l-hydroxyalkyl)pyrroles (e.g. 139). The intermediate oxetane undergoes rearrangement under the reaction conditions (79JOC2949). [Pg.67]

Pyrazolones show a great variety of reactions with carbonyl compounds (B-76MI40402). For instance, antipyrine is 4-hydroxymethylated by formaldehyde and it also undergoes the Mannich reaction. Tautomerizable 2-pyrazolin-5-ones react with aldehydes to yield compound (324) and with acetone to form 4-isopropylidene derivatives or dimers (Scheme 8 Section 4.02.1.4.10). [Pg.242]

Titanium(IV) is a powerful but selective Lewis acid which can promote the coupling of allylsilanes with carbonyl compounds and derivatives In the presence of titanium tetrachlonde, benzalacetone reacts with allyltnmethylsilane by 1,4-addition to give 4-PHENYL-6-HEPTEN-2-ONE. Similarly, the enol silyl ether of cyclopentanone is coupled with f-pentyl chloride using titanium tetrachlonde to give 2-(tert-PENTYL)CYCLOPENTANONE, an example of a-tert-alkylation of ketones. [Pg.225]

The stereoselectivity of organometallic additions with carbonyl compounds fits into the general pattern for nucleophilic attack discussed in Chapter 3. With 4-r-butylcyclohex-anone, there is a preference for equatorial approach but the selectivity is low. Enhanced steric factors promote stereoselective addition. [Pg.466]

Enolates can also serve as carbon nucleophiles in carbonyl addition reactions. The addition reaction of enolates with carbonyl compounds is of very broad scope and is of great synthetic importance. Essentially all of the enolates considered in Chapter 7 are capable of adding to carbonyl groups. The reaction is known as the generalized aldol addition. [Pg.466]

Aminodiphenyl reacts with carbonyl compounds to form colored or fluorescent Schiff s bases with the elimination of water ... [Pg.158]

These reactions differ from those of sulfur tetrafluoride with carbonyl compounds in that a formal oxidation-reduction of the sulfur atoms m the thiocarbonyl compound and sulfur tetrafluoride molecule occurs, resulting in the formation of free sulfur and the complete utilization of the fluorine atoms in sulfur tetrafluoride. [Pg.267]

Convenient syntheses of vinyl fluorides are of synthetic interest, fhe conjugate base of fluoromethyl phenyl sulfone reacts with carbonyl compounds to provide P-tluoro alcohols, which are used to prepare terminal vinyl fluorides [25] (equation 23) (Table 9) This reaction offers an alternative to the Winig reaction, which may be very sensitive to reaction conditions. [Pg.570]


See other pages where With Carbonyl Compounds is mentioned: [Pg.226]    [Pg.1125]    [Pg.573]    [Pg.712]    [Pg.9]    [Pg.12]    [Pg.340]    [Pg.35]    [Pg.552]    [Pg.557]    [Pg.607]    [Pg.635]    [Pg.650]    [Pg.650]    [Pg.650]    [Pg.650]    [Pg.651]    [Pg.735]    [Pg.777]    [Pg.780]    [Pg.782]    [Pg.819]    [Pg.825]    [Pg.825]    [Pg.416]    [Pg.236]   


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1,3-Pentadiene reactions with carbonyl compounds

1.3- Butadiene reactions with carbonyl compounds

1.3- Oxazine, dihydroreaction with carbonyl compounds

1.3- Oxazine, dihydroreaction with carbonyl compounds preparation

1.3- Oxazine, dihydroreaction with carbonyl compounds two-carbon homologation

2-Azapentadienyl anion reaction with carbonyl compounds

Acetylides reactions with carbonyl compounds

Alcohols by reduction of carbonyl compounds with

Alcohols from Reaction of Carbonyl Compounds with Grignard Reagents

Alcohols reaction with carbonyl compound

Alkenes from carbonyl compounds with

Alkenes reductive coupling with carbonyl compounds

Alkenes with carbonyl compounds

Alkyl metals, 1-silyl-1-selenoreactions with carbonyl compounds

Alkyl metals, a-selenocarbonyl compound homologation reactions with carbonyl compounds

Alkyl metals, a-selenoxyreactions with carbonyl compounds

Alkylation with Carbonyl Compounds The Prins Reaction

Alkylation with Carbonyl Compounds and Derivatives

Alkylidenation of Carbonyl Compounds with Dialkyltitanocenes and Related Complexes

Alkynes with carbonyl compounds

Allene, reaction with carbonyl compounds

Allenes with carbonyl compounds

Allyl acetates reactions with carbonyl compounds

Allyl reaction with carbonyl compounds

Allylation reactions with carbonyl compounds

Allylic acetates reactions with carbonyl compounds

Allylic alcohols coupling with carbonyl compounds

Allylsilanes reactions with carbonyl compounds

Allylstannanes reactions with carbonyl compounds

Allylthiol reactions with carbonyl compounds

Aluminum, triethylreaction of allylic anions with carbonyl compounds

Aluminum, triethylreaction of allylic anions with carbonyl compounds regioselectivity

Amines react with carbonyl compounds

Amines reaction with carbonyl compounds

Amino reaction with carbonyl compound

Aromatic hydrocarbons with carbonyl compounds

Arsonium ylides reaction with carbonyl compounds

Benzothiazole, 2-alkylmetallated reactions with carbonyl compounds

Biphilic Reactions with Carbonyl Compounds

Borane, dialkylcrotylisomerization reactions with carbonyl compounds

Boranes reaction with halo carbonyl compounds

Borohydride reaction with carbonyl compounds

Carbanions addition reactions with carbonyl compounds

Carbene complexes reactions with carbonyl compounds

Carbene complexes, alkyl pentacarbonylalkylation reaction with carbonyl compounds

Carbonyl Compounds amines with

Carbonyl Compounds bisulphite with

Carbonyl complexes, reaction with organomagnesium compound

Carbonyl compounds 1,4-addition reactions with

Carbonyl compounds 1,4-addition reactions with cyanohydrin ethers

Carbonyl compounds 1,4-addition reactions with cyanohydrins

Carbonyl compounds 2+2]-photocycloaddition with alkenes

Carbonyl compounds a-diazoreaction with trialkylboranes

Carbonyl compounds acid derivatives reactions with organometallic reagents

Carbonyl compounds addition reactions with alcohols

Carbonyl compounds cycloaddition with alkenes

Carbonyl compounds interaction with Lewis acids

Carbonyl compounds photochemical cycloaddition with

Carbonyl compounds photocycloaddition reactions with alkenes

Carbonyl compounds reaction with alanines

Carbonyl compounds reaction with alcohols to form hemiacetal

Carbonyl compounds reaction with benzylic

Carbonyl compounds reaction with bisulfite

Carbonyl compounds reaction with boron reagents

Carbonyl compounds reaction with cyanide

Carbonyl compounds reaction with diazoalkanes

Carbonyl compounds reaction with enol silanes

Carbonyl compounds reaction with nitriles

Carbonyl compounds reaction with organocuprates

Carbonyl compounds reaction with sodium borohydrid

Carbonyl compounds reaction with sodium borohydride

Carbonyl compounds reaction with trialkylboranes

Carbonyl compounds reaction with water

Carbonyl compounds reactions with a-selenoalkylmetals

Carbonyl compounds reactions with allenylsilanes

Carbonyl compounds reactions with allylic sulfinyl carbanions

Carbonyl compounds reactions with crotyl organometallics

Carbonyl compounds reactions with nucleophile

Carbonyl compounds reactions with nucleophiles

Carbonyl compounds reactions with organometallic reagents

Carbonyl compounds reactions with organometallics

Carbonyl compounds reactions with organosamarium ‘ate’ complexes

Carbonyl compounds reactions with selenium-stabilized carbanions

Carbonyl compounds reactions with sulfonimidoyl carbanions

Carbonyl compounds reactions with sulfonyl-stabilized carbanions

Carbonyl compounds reductive coupling with activated alkenes

Carbonyl compounds with NADH model

Carbonyl compounds with acetylide ions

Carbonyl compounds with diazomethane

Carbonyl compounds with metal hydride reagents

Carbonyl compounds with nitrogen nucleophiles

Carbonyl compounds with nitrosobenzene

Carbonyl compounds with nucleophiles

Carbonyl compounds with organometallic reagents

Carbonyl compounds, a-seleno reactions with enals

Carbonyl compounds, reaction with ammonia

Carbonyl compounds, reaction with hydrazine

Carbonyl compounds, reaction with methylene equivalents

Carbonyl compounds, reaction with phosphines

Carbonyl compounds, reactions with organolithiums or Grignard reagents

Carbonyl compounds, reactions with silenes

Carbonyl group, compounds with

Chromium, propargylreactions with carbonyl compounds

Cobalt, octacarbonylbiscatalyst silane reaction with carbonyl compounds

Condensation of Phosphonium Ylides with Carbonyl Compounds Wittig Reaction

Condensation with carbonyl compounds

Conjugated carbonyl compounds, reduction with

Coupling of Activated Aliphatic Halides with Carbonyl Compounds

Cumulative Subject reaction with carbonyl compounds

Cyanohydrin esters reactions with carbonyl compounds

Cyanohydrin ethers reactions with carbonyl compounds

Cycloaddition Reactions of Carbonyl Compounds with Alkenes

Cyclopropanecarboxylic acid, 2-silyloxyhomoenolate equivalents reactions with carbonyl compounds

Diazo compounds, reactions with metal carbonyls

Diazo reaction with carbonyl compounds

Diazoalkanes, preparation with carbonyl compounds

Diols reaction with carbonyl compounds

Disilene with carbonyl compounds

Enol esters reaction with carbonyl compounds

Enol ethers reaction with carbonyl compounds

Enol sulfonates reaction with carbonyl compounds

Enolates reaction with carbonyl compounds

Enolates with carbonyl compounds

Enols, equilibrium with carbonyl compounds

Ether, benzyl chloromethyl reaction with carbonyl compounds

Evidence for equilibration of carbonyl compounds with enols

Formation by Condensation of an Amine with a Carbonyl Compound

From Other Carbonyl-Containing Compounds with Perfluoroalkyl Groups

Functional group compounds with carbonyl groups

Furan, 2,5-bis reaction with carbonyl compounds

Furan, 2,5-bis reaction with carbonyl compounds from succinic anhydrides

Furan, 2,5-bis reaction with carbonyl compounds synthesis

Furan, 2,5-bis reaction with carbonyl compounds titanium tetrachloride catalyst

Furan, 2-trimethylsiloxyaldol condensation reaction with carbonyl compounds

Grignard reaction: alkylation with carbonyl compounds

Grignard reagents reaction with carbonyl compounds

Homoenolates reaction with carbonyl compounds

Hydrazones reaction with carbonyl compounds

Hydride shifts reactions with carbonyl compounds

Hydrogen sulfide, addition with carbonyl compounds

Hydroxy Alkylation with Carbonyl Compounds

Hydroxyalkylation with Carbonyl Compounds

Hydroxylamine, reaction with carbonyl compounds

Indoles with conjugated carbonyl compounds

Iodides reactions with carbonyl compounds

Iron, carbonyl compounds reaction with base

Isoprene reactions with carbonyl compounds

Isoquinoline reactions with carbonyl compounds

Ketenes reaction with carbonyl compounds

Lanthanide homoenolates reactions with carbonyl compounds

Lithium aluminum hydride reduction, alcohols from, with carbonyl compounds

Lithium dialkylcuprates reactions with carbonyl compounds

Lithium, 1-phenylseleno-l-thioalkylreactivity reactions with carbonyl compounds

Lithium, 1-seleno-1-silylalkylreactivity reactions with carbonyl compounds

Lithium, a-selenoalkylacyl anion equivalents reactions with carbonyl compounds

Lithium, a-selenoalkylnucleophilicity reactions with carbonyl compounds

Lithium, a-selenoallylambident reactivity reactions with carbonyl compounds

Lithium, a-selenocyclopropylreactivity reactions with carbonyl compounds

Lithium, trialkylstannylmethylreactions with carbonyl compounds

Lithium, trialkylstannylmethylreactions with carbonyl compounds methylenation

Lithium, triarylstannylmethylreactions with carbonyl compounds

Lithium, triarylstannylmethylreactions with carbonyl compounds methylenation

Magnesium bromide allylstannane reaction with carbonyl compounds

Manganese, alkylreactions with carbonyl compounds

Manganese, alkylreactions with carbonyl compounds Lewis acid promotion

Metallates with carbonyl compounds

Methanesulfonic acid reactions with carbonyl compounds

Methanethiol, phenyldianions reactions with carbonyl compounds

Methyl group, reactivity with carbonyl compounds

Nickel sulfide silane reaction with carbonyl compounds

Nucleophilic addition with carbonyl compounds

Organic chemistry compounds with carbonyl

Organic chemistry compounds with carbonyl group

Organocadmium reagents reactions with carbonyl compounds

Organochromium reagents reactions with carbonyl compounds

Organolithium reagents reactions with carbonyl compounds

Organolithium with carbonyl compounds

Organolithiums reaction with carbonyl compounds

Organomagnesium reagents reactions with carbonyl compounds

Organometallic compounds with conjugated carbonyl

Organometallic compounds, reactions with carbonyls

Organosilanes reactions with carbonyl compounds

Organostannanes reactions with carbonyl compounds

Organotin compounds reactions with carbonyls

Organotitanium reagents reactions with carbonyl compounds

Organozinc reagents reactions with carbonyl compounds

Oxazoline, 2-alkylmetallated achiral reactions with carbonyl compounds

Oxidation of Alcohols to Carbonyl Compounds with Activated Dimethyl Sulfoxide via Alkoxysulfonium Ylides. The Swern, Moffatt, and Related Oxidations

Oxidation with carbonyl compounds

Phenylhydrazine reaction with carbonyl compounds

Photochemical cycloaddition reactions of carbonyl compounds with alkenes

Photochemical cycloadditions with carbonyl compounds

Pinacol coupling reactions with carbonyl compounds

Propargylation carbonyls, with indium compounds

Propargylic acetates reactions with carbonyl compounds

Propionic acid reactions with carbonyl compounds

Propionic acid, 3- dianions reactions with carbonyl compounds

Propyne, l,3-bis dilithium anion reaction with aliphatic carbonyl compounds

Pyrrole direct coupling with carbonyl compounds

Pyrrole, 2,5-bis reaction with carbonyl compounds

Reaction of carbonyl compounds with sulfur tetrafluoride

Reaction of stabilized carbanions with carbonyl compounds

Reaction with Carbonyl Compounds 2 Imines

Reaction with carbonyl compounds

Reactions of Carbonyl Compounds with Heteroatom Nucleophiles

Reactions of Carbonyl Compounds with Other Carbon Nucleophiles

Reactions of Carbonyl Compounds with a-Trimethylsilylcarbanions

Reactions of Co-ordinated Carbonyl Compounds with Nucleophiles

Reactions of Organolithiums with Carbonyl Compounds

Reactions with Chiral Non-Racemic Carbonyl Compounds

Reactions with Prochiral Carbonyl Compounds

Reactions with a, 3-Unsaturated Carbonyl Compounds

Reactions with carbonyl compounds aromatic aldehydes

Reactions with carbonyl compounds ketones

Reactions with carbonyl compounds mechanism

Reactions with carbonyl compounds olefin yields

Reactions with carbonyl compounds product isomerization

Reduction of Carbonyl Compounds with Aluminum Alkoxides

Reductive Alkylation of Ammonia with Carbonyl Compounds

Reductive Alkylation of Primary Amines with Carbonyl Compounds

Reductive N-Alkylation of Primary Amides with Carbonyl Compounds

Reversibility with carbonyl compounds

Rhodium, chlorotris catalyst silane reaction with carbonyl compounds

Samarium, allylreactions with carbonyl compounds

Samarium, benzylreactions with carbonyl compounds

Schmidt reactions with carbonyl compounds

Secondary with carbonyl compounds

Selenides, p-hydroxyalkyl reactions with carbonyl compounds

Selenones, a-metalloalkyl reactions with carbonyl compounds

Selenonium ylides reactions with carbonyl compounds

Selenoxides, a-metalloalkyl reactions with carbonyl compounds

Selenoxides, a-metallovinyl reactions with carbonyl compounds

Silane, vinylepoxidation reaction with carbonyl compounds

Silanes reaction with carbonyl compounds

Silanes, allenyl annulations reactions with a,p-unsaturated carbonyl compounds

Silanones reactions with carbonyl compounds

Silyl cyanides, trialkylreactions with carbonyl compounds

Silyl cyanides, trialkylreactions with carbonyl compounds Lewis acid promotion

Silyl enol ethers reactions with carbonyl compounds

Silyl enol ethers with carbonyl compounds

Silylenes with carbonyl compounds

Sodium bisulfite, reaction with carbonyl compounds

Stabilized carbanions with carbonyl compounds

Stannanes reactions with carbonyl compounds

Stereoelectronics reactions of chiral carbonyl compounds with

Stereoselectivity with carbonyl compounds

Subject reactions with carbonyl compounds

Substrate Control with Chiral Carbonyl Compounds

Sulfones, a-haloreactions with carbonyl compounds

Sulfoxide, benzyl f-butyl reactions with carbonyl compounds

Sulfoxide, methyl p-tolyl reactions with carbonyl compounds

Sulfoxides, a-halo reactions with carbonyl compounds

Sulfoxides, alkyl aryl reactions with carbonyl compounds

Sulfoxides, allyl p-tolyl reactions with carbonyl compounds

Sulfur ylides reactions with carbonyl compounds

The Exchange of Carbonyl Compounds with Water

The Reactions of Carbonyl Compounds with Hydride Ion

The interaction of carbonyl-containing compounds with organometallic reagents

Thioanisole reaction with carbonyl compounds

Tin, bis diiodoreaction with carbonyl compounds

Tin, trialkylaminoreaction with carbonyl compounds

Tin, trialkylaminoreaction with carbonyl compounds preparation of enol stannyl ethers

Titanium complexes reactions with carbonyl compounds

Titanium compounds carbonyls with alkenes

Titanium tetrachloride allylstannane reactions with carbonyl compounds

Titanium tetrachloride reactions with carbonyl compounds

Titanium, alkylreactions with carbonyl compounds

Titanium, ally 1heterosubstituted reactions with carbonyl compounds

Titanium, allylheterosubstituted reactions with carbonyl compounds

Titanium, allylreactions with carbonyl compounds

Titanium, arylreactions with carbonyl compounds

Titanium, crotylreactions with carbonyl compounds

Titanium, dichlorodimethylreaction with carbonyl compounds

Titanium, dichlorodimethylreaction with carbonyl compounds chemoselectivity

Titanium, dichlorodiphenylreaction with carbonyl compounds

Titanium, dichlorodiphenylreaction with carbonyl compounds chemoselectivity

Titanium, dienylreactions with carbonyl compounds

Titanium, methyl reactions with carbonyl compounds

Titanium, propargylreactions with carbonyl compounds

Titanium, trichloromethylproperties reaction with carbonyl compounds

Titanium, tris methylproperties reaction with carbonyl compounds

Titanocene, crotylreaction with carbonyl compounds

Titanocene, crotylreaction with carbonyl compounds synthesis

Tosylates reactions with carbonyl compounds

Unsaturated carbonyl compounds reaction with organocopper reagents

Vinylaminodichloroboranes with carbonyl compounds

Ylides reactions with carbonyl compounds

Ynamines reactions with carbonyl compounds

Zirconium reagents, allylic reaction with carbonyl compounds

Zirconium, alkylreactions with carbonyl compounds

Zirconium, alkyltributoxyreaction with carbonyl compounds

Zirconium, alkyltributoxyreaction with carbonyl compounds chemoselectivity

Zirconium, arylreactions with carbonyl compounds

Zirconium, aryltributoxyreaction with carbonyl compounds

Zirconium, aryltributoxyreaction with carbonyl compounds chemoselectivity

Zirconium, dienylreactions with carbonyl compounds

Zirconium, tetraallylreaction with carbonyl compounds

Zirconocene, crotylreaction with carbonyl compounds

Zirconocene, crotylreaction with carbonyl compounds synthesis

Zirconocene, dienereactions with carbonyl compounds

Zirconocene, isoprenereactions with carbonyl compounds

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