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26 relations: Alkene, Amine, Benzeneselenol, Carbonyl group, Chemical compound, Debye, Dichloromethane, Diphenyl disulfide, Enol, Epoxide, Grignard reaction, Haloalkane, Halogenation, Journal of the American Chemical Society, Lactam, Magnesium bromide, Mesylate, Nucleophilic substitution, Organic Reactions, Organic synthesis, Organolithium reagent, Phenyl group, Phenylmagnesium bromide, Silyl enol ether, Tetrahedron (journal), Tosyl.
Alkene
In organic chemistry, an alkene is an unsaturated hydrocarbon that contains at least one carbon–carbon double bond.
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Amine
In organic chemistry, amines are compounds and functional groups that contain a basic nitrogen atom with a lone pair.
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Benzeneselenol
Benzeneselenol, also known as selenophenol, is the organoselenium compound with the formula C6H5SeH, often abbreviated PhSeH.
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Carbonyl group
In organic chemistry, a carbonyl group is a functional group composed of a carbon atom double-bonded to an oxygen atom: C.
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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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Debye
The debye (symbol: D) is a CGS unit (a non-SI metric unit) of electric dipole momentElectric dipole moment is defined as charge times displacement: |- |height.
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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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Diphenyl disulfide
Diphenyl disulfide is the chemical compound with the formula (C6H5S)2.
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Enol
Enols, or more formally, alkenols, are a type of reactive structure or intermediate in organic chemistry that is represented as an alkene (olefin) with a hydroxyl group attached to one end of the alkene double bond.
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Epoxide
An epoxide is a cyclic ether with a three-atom ring.
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Grignard reaction
The Grignard reaction (pronounced) is an organometallic chemical reaction in which alkyl, vinyl, or aryl-magnesium halides (Grignard reagents) add to a carbonyl group in an aldehyde or ketone.
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Haloalkane
The haloalkanes (also known as halogenoalkanes or alkyl halides) are a group of chemical compounds derived from alkanes containing one or more halogens.
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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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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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Lactam
A lactam is a cyclic amide.
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Magnesium bromide
Magnesium bromide (MgBr2) is a chemical compound of magnesium and bromine that is white and deliquescent.
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Mesylate
In chemistry, a mesylate is any salt or ester of methanesulfonic acid (CH3SO3H).
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Nucleophilic substitution
In organic and inorganic chemistry, nucleophilic substitution is a fundamental class of reactions in which an electron rich nucleophile selectively bonds with or attacks the positive or partially positive charge of an atom or a group of atoms to replace a leaving group; the positive or partially positive atom is referred to as an electrophile.
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Organic Reactions
Organic Reactions is a secondary reference which synthesizes the organic chemistry literature around particular chemical transformations.
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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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Organolithium reagent
Organolithium reagents are organometallic compounds that contain carbon – lithium bonds.
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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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Phenylmagnesium bromide
Phenylmagnesium bromide, with the simplified formula, is a magnesium-containing organometallic compound.
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Silyl enol ether
Silyl enol ethers in organic chemistry are a class of organic compounds that share a common functional group composed of an enolate bonded through its oxygen end to an organosilicon group.
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Tetrahedron (journal)
Tetrahedron is a weekly peer-reviewed scientific journal covering the field of organic chemistry.
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Tosyl
A toluenesulfonyl (shortened tosyl, abbreviated Ts or Tos) group is CH3C6H4SO2.
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Diphenyldiselenide, N-PSP, Ph2Se2, Phenyl diselenide, Phenyldiselenide.
References
[1] https://en.wikipedia.org/wiki/Diphenyl_diselenide
