Anagram & Information om | Engelska ordet ARYL
ARYL
Antal bokstäver
4
Är palindrom
Nej
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Exempel på hur du använder ARYL i en mening
- In organic chemistry, an aryl is any functional group or substituent derived from an aromatic ring, usually an aromatic hydrocarbon, such as phenyl and naphthyl.
- ABC-Transporter Genes - abl gene - acetic acid - acetyl CoA - acetylcholine - acetylcysteine - acid - acidic fibroblast growth factor - acrosin - actin - action potential - activation energy - active site - active transport - adenosine - adenosine diphosphate (ADP) - adenosine monophosphate (AMP) - adenosine triphosphate (ATP) - adenovirus - adrenergic receptor - adrenodoxin - aequorin - aerobic respiration - agonist - alanine - albumin - alcohol - alcoholic fermentation - alicyclic compound - aliphatic compound - alkali - allosteric site - allostery - allotrope - allotropy - alpha adrenergic receptor - alpha helix - alpha-1 adrenergic receptor - alpha-2 adrenergic receptor - alpha-beta T-cell antigen receptor - alpha-fetoprotein - alpha-globulin - alpha-macroglobulin - alpha-MSH - Ames test - amide - amine - amino - amino acid - amino acid receptor - amino acid sequence - amino acid sequence homology - aminobutyric acid - ammonia - AMPA receptor - amyloid - anabolism - anaerobic respiration - analytical chemistry - androgen receptor - angiotensin - angiotensin II - angiotensin receptor - ankyrin - annexin II - antibiotic - antibody - apoenzyme - apolipoprotein - apoptosis - aquaporin - archaea - arginine - argipressin - aromatic amine - aromatic compound - arrestin - Arrhenius equation - aryl hydrocarbon receptor - asparagine - aspartic acid - atom - atomic absorption spectroscopy - atomic mass - atomic mass unit - atomic nucleus - atomic number - atomic orbital - atomic radius - Atomic weight - ATP synthase - ATPase - atrial natriuretic factor - atrial natriuretic factor receptor - Avogadro constant - axon.
- In organic chemistry, an aryl halide (also known as haloarene) is an aromatic compound in which one or more hydrogen atoms, directly bonded to an aromatic ring are replaced by a halide.
- His name is associated with the Gomberg-Bachmann reaction for the synthesis of diaryl compounds from aryl diazonium chlorides.
- Aromatic azo compounds can be synthesized by azo coupling, which entails an electrophilic substitution reaction where an aryl diazonium cation is attacked by another aryl ring, especially those substituted with electron-donating groups:.
- 6π electrocyclizations of the Z form, leading to an additional bond between the two aryl functionalities and a disruption of the aromatic character of these groups.
- There are many derivatives of the parent phthalocyanine, where either carbon atoms of the macrocycle are exchanged for nitrogen atoms or the peripheral hydrogen atoms are substituted by functional groups like halogens, hydroxyl, amine, alkyl, aryl, thiol, alkoxy and nitrosyl groups.
- While initial research in the field focused on the coupling of alkyl groups, most future work involved the much more synthetically useful coupling of vinyl, alkenyl, aryl, and allyl organostannanes to halides.
- The catalytically active palladium species A is coupled with the aryl halide substrate 1 to yield an organopalladium complex B.
- In organic chemistry, quaternary ammonium cations, also known as quats, are positively-charged polyatomic ions of the structure , where R is an alkyl group, an aryl group or organyl group.
- Bromobenzene is an aryl bromide and the simplest of the bromobenzenes, consisting of a benzene ring substituted with one bromine atom.
- In the Sandmeyer reaction, the treatment of an arenediazonium salt with CuCl leads to an aryl chloride.
- Condensation with two aryl- or alkylamines gives NacNacs, wherein the oxygen atoms in acetylacetone are replaced by NR (R = aryl, alkyl).
- The Sandmeyer reaction is a chemical reaction used to synthesize aryl halides from aryl diazonium salts using copper salts as reagents or catalysts.
- alt=A macrocyclization: a 1,5-pentanedithiol terminus attacks the butadiene tail of a 1-substituted 2,4-pentadien-2-yl aryl ketone.
- Combined with electrophilic aryl halides, N-tosylhydrazones can be used to prepare polysubstituted olefins under Pd-catalyzed conditions without the use of often expensive, and synthetically demanding organometallic reagents.
- The Bouveault aldehyde synthesis (also known as the Bouveault reaction) is a one-pot substitution reaction that replaces an alkyl or aryl halide with a formyl group using a N,N-disubstituted formamide.
- Chlorobenzene (abbreviated PhCl) is an aryl chloride and the simplest of the chlorobenzenes, consisting of a benzene ring substituted with one chlorine atom.
- The Japp–Klingemann reaction is a chemical reaction used to synthesize hydrazones from β-keto-acids (or β-keto-esters) and aryl diazonium salts.
- This method has been utilized to produce a variety of kinetically stable phosphaalkynes, including aryl, tertiary alkyl, secondary alkyl, and even primary alkyl phosphaalkynes in good yields.
Förberedelsen av sidan tog: 100,75 ms.