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Schwartz's reagent

Index Schwartz's reagent

Schwartz's reagent is the common name for the chemical compound with the formula (C5H5)2ZrHCl, sometimes called zirconocene hydrochloride or zirconocene chloride hydride, and is named after Jeffrey Schwartz, a chemistry professor at Princeton University. [1]

61 relations: Acyl chloride, Acyl group, Alcohol, Aldehyde, Alkane, Alkene, Alkyne, Allyl alcohol, Amide, Angewandte Chemie, Bromine, Carbon monoxide, Carbonylation, ChemComm, Chemical compound, Cis–trans isomerism, Computational chemistry, Coupling reaction, Cyclopropane, Diastereomer, Dichloromethane, Diphenylacetylene, Electrophile, Empirical formula, Ester, Halogenation, Hydrochloric acid, Hydrometalation, Iodane, Iodine, Journal of Organic Chemistry, Journal of Organometallic Chemistry, Journal of the American Chemical Society, Journal of the Chemical Society, Ketone, Lithium aluminium hydride, Lithium tetrachloroaluminate, Macrolide, Metallocene, Nucleophilic addition, Nucleophilic conjugate addition, One-pot synthesis, Organic Syntheses, Organic synthesis, Organoaluminium chemistry, Organoboron chemistry, Organobromine compound, Organometallics, Phenyl group, Phenylacetylene, ..., Princeton University, Pure and Applied Chemistry, Pyrophoricity, Reducing agent, Regioselectivity, Tetrafluoroborate, Tetrahedron (journal), Thermodynamic versus kinetic reaction control, Transmetalation, Zinc chloride, Zirconocene dichloride. Expand index (11 more) »

Acyl chloride

In organic chemistry, an acyl chloride (or acid chloride) is an organic compound with the functional group -COCl. Their formula is usually written RCOCl, where R is a side chain.

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Acyl group

An acyl group is a moiety derived by the removal of one or more hydroxyl groups from an oxoacid, including inorganic acids.

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Alcohol

In chemistry, an alcohol is any organic compound in which the hydroxyl functional group (–OH) is bound to a carbon.

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Aldehyde

An aldehyde or alkanal is an organic compound containing a functional group with the structure −CHO, consisting of a carbonyl center (a carbon double-bonded to oxygen) with the carbon atom also bonded to hydrogen and to an R group, which is any generic alkyl or side chain.

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Alkane

In organic chemistry, an alkane, or paraffin (a historical name that also has other meanings), is an acyclic saturated hydrocarbon.

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Alkene

In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.

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Alkyne

In organic chemistry, an alkyne is an unsaturated hydrocarbon containing at least one carbon—carbon triple bond.

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Allyl alcohol

Allyl alcohol (IUPAC name: prop-2-en-1-ol) is an organic compound with the structural formula CH2.

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Amide

An amide (or or), also known as an acid amide, is a compound with the functional group RnE(O)xNR′2 (R and R′ refer to H or organic groups).

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Angewandte Chemie

Angewandte Chemie (meaning "Applied Chemistry") is a weekly peer-reviewed scientific journal that is published by Wiley-VCH on behalf of the German Chemical Society (Gesellschaft Deutscher Chemiker).

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Bromine

Bromine is a chemical element with symbol Br and atomic number 35.

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Carbon monoxide

Carbon monoxide (CO) is a colorless, odorless, and tasteless gas that is slightly less dense than air.

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Carbonylation

Carbonylation refers to reactions that introduce carbon monoxide into organic and inorganic substrates.

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ChemComm

ChemComm (or Chemical Communications), formerly known as Journal of the Chemical Society D: Chemical Communications (1969–1971), Journal of the Chemical Society, Chemical Communications (1972–1995), is a peer-reviewed scientific journal published by the Royal Society of Chemistry.

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Chemical compound

A chemical compound is a chemical substance composed of many identical molecules (or molecular entities) composed of atoms from more than one element held together by chemical bonds.

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Cis–trans isomerism

Cis–trans isomerism, also known as geometric isomerism or configurational isomerism, is a term used in organic chemistry.

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Computational chemistry

Computational chemistry is a branch of chemistry that uses computer simulation to assist in solving chemical problems.

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Coupling reaction

A coupling reaction in organic chemistry is a general term for a variety of reactions where two hydrocarbon fragments are coupled with the aid of a metal catalyst.

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Cyclopropane

Cyclopropane is a cycloalkane molecule with the molecular formula C3H6, consisting of three carbon atoms linked to each other to form a ring, with each carbon atom bearing two hydrogen atoms resulting in D3h molecular symmetry.

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Diastereomer

Diastereomers (sometimes called diastereoisomers) are a type of a stereoisomer.

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Dichloromethane

Methylene dichloride (DCM, or methylene chloride, or dichloromethane) is a geminal organic compound with the formula CH2Cl2.

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Diphenylacetylene

Diphenylacetylene is the chemical compound C6H5C≡CC6H5.

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Electrophile

In organic chemistry, an electrophile is a reagent attracted to electrons.

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Empirical formula

In chemistry, the empirical formula of a chemical compound is the simplest positive integer ratio of atoms present in a compound.

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Ester

In chemistry, an ester is a chemical compound derived from an acid (organic or inorganic) in which at least one –OH (hydroxyl) group is replaced by an –O–alkyl (alkoxy) group.

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Halogenation

Halogenation is a chemical reaction that involves the addition of one or more halogens to a compound or material.

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Hydrochloric acid

Hydrochloric acid is a colorless inorganic chemical system with the formula.

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Hydrometalation

Hydrometalation (hydrometallation) is a type of chemical reaction in organometallic chemistry in which a chemical compound with a hydrogen to metal bond (M-H, metal hydride) adds to compounds with an unsaturated bond like an alkene (RC.

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Iodane

Iodanes are chemical compounds containing hypervalent iodine.

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Iodine

Iodine is a chemical element with symbol I and atomic number 53.

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Journal of Organic Chemistry

The Journal of Organic Chemistry, colloquially known as JOC or J Org, is a peer-reviewed scientific journal for original contributions of fundamental research in all branches of theory and practice in organic and bioorganic chemistry.

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Journal of Organometallic Chemistry

The Journal of Organometallic Chemistry is a peer-reviewed scientific journal published by Elsevier, covering research on organometallic chemistry.

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Journal of the American Chemical Society

The Journal of the American Chemical Society (also known as JACS) is a weekly peer-reviewed scientific journal that was established in 1879 by the American Chemical Society.

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Journal of the Chemical Society

The Journal of the Chemical Society was a scientific journal established by the Chemical Society in 1849 as the Quarterly Journal of the Chemical Society.

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Ketone

In chemistry, a ketone (alkanone) is an organic compound with the structure RC(.

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Lithium aluminium hydride

Lithium aluminium hydride, commonly abbreviated to LAH, is an inorganic compound with the chemical formula LiAlH4.

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Lithium tetrachloroaluminate

Lithium tetrachloroaluminate (LAC, lithium aluminium chloride) is an inorganic compound, a tetrachloroaluminate of lithium, with the formula LiAlCl4.

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Macrolide

The macrolides are a class of natural products that consist of a large macrocyclic lactone ring to which one or more deoxy sugars, usually cladinose and desosamine, may be attached.

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Metallocene

A metallocene is a compound typically consisting of two cyclopentadienyl anions (abbreviated Cp) bound to a metal center (M) in the oxidation state II, with the resulting general formula (C5H5)2M.

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Nucleophilic addition

In organic chemistry, a nucleophilic addition reaction is an addition reaction where a chemical compound with an electron-deficient or electrophilic double or triple bond, a π bond, reacts with electron-rich reactant, termed a nucleophile, with disappearance of the double bond and creation of two new single, or σ, bonds.

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Nucleophilic conjugate addition

Nucleophilic conjugate addition is a type of organic reaction.

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One-pot synthesis

In chemistry a one-pot synthesis is a strategy to improve the efficiency of a chemical reaction whereby a reactant is subjected to successive chemical reactions in just one reactor.

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Organic Syntheses

Organic Syntheses is a peer-reviewed scientific journal that was established in 1921.

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Organic synthesis

Organic synthesis is a special branch of chemical synthesis and is concerned with the intentional construction of organic compounds.

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Organoaluminium chemistry

Organoaluminium chemistry is the study of compounds containing bonds between carbon and aluminium bond.

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Organoboron chemistry

Organoborane or organoboron compounds are chemical compounds of boron and carbon that are organic derivatives of BH3, for example trialkyl boranes.

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Organobromine compound

Organobromine compounds, also called organobromides, are organic compounds that contain carbon bonded to bromine.

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Organometallics

Organometallics is a biweekly journal published by the American Chemical Society.

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Phenyl group

In organic chemistry, the phenyl group or phenyl ring is a cyclic group of atoms with the formula C6H5.

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Phenylacetylene

Phenylacetylene is an alkyne hydrocarbon containing a phenyl group.

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Princeton University

Princeton University is a private Ivy League research university in Princeton, New Jersey.

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Pure and Applied Chemistry

Pure and Applied Chemistry (abbreviated Pure Appl. Chem.) is the official journal for the International Union of Pure and Applied Chemistry (IUPAC).

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Pyrophoricity

A pyrophoric substance (from Greek πυροφόρος, pyrophoros, "fire-bearing") ignites spontaneously in air at or below 55 °C (130 °F).

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Reducing agent

A reducing agent (also called a reductant or reducer) is an element (such as calcium) or compound that loses (or "donates") an electron to another chemical species in a redox chemical reaction.

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Regioselectivity

In chemistry, regioselectivity is the preference of one direction of chemical bond making or breaking over all other possible directions.

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Tetrafluoroborate

Tetrafluoroborate is the anion BF4−.

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Tetrahedron (journal)

Tetrahedron is a weekly peer-reviewed scientific journal covering the field of organic chemistry.

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Thermodynamic versus kinetic reaction control

Thermodynamic reaction control or kinetic reaction control in a chemical reaction can decide the composition in a reaction product mixture when competing pathways lead to different products and the reaction conditions influence the selectivity or stereoselectivity.

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Transmetalation

Transmetalation (alt. spelling: transmetallation) is a type of organometallic reaction that involves the transfer of ligands from one metal to another.

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Zinc chloride

Zinc chloride is the name of chemical compounds with the formula ZnCl2 and its hydrates.

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Zirconocene dichloride

Zirconocene dichloride is an organozirconium compound composed of a zirconium central atom, with two cyclopentadienyl and two chloro ligands.

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Redirects here:

Cp2ZrClH, Hydrozirconation, Schwartz reagent, Schwartz's Reagent, Zirconocene chloride hydride, Zirconocene hydride, Zirconocene hydrochloride.

References

[1] https://en.wikipedia.org/wiki/Schwartz's_reagent

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