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106 relations: Acetaldehyde, Acetone, Acetophenone, Aconitine, Albert Eschenmoser, Aldehyde, Aldol, Aldol reaction, Alexander Dianin, Auwers synthesis, Étard reaction, Baeyer–Drewson indigo synthesis, Barium hydroxide, Benzaldehyde, Benzil, Benzoin condensation, Benzylideneacetone, Benzyltrimethylammonium hydroxide, Beta-Hydroxy beta-methylbutyric acid, Biginelli reaction, Biosynthesis of doxorubicin, Capnellene, Carbonyl group, Chalcone, Chichibabin pyridine synthesis, Cholesterol total synthesis, Cinnamaldehyde, Cinnamic acid, Citrate synthase, Citric acid cycle, Claisen condensation, Condensation reaction, Crotonaldehyde, Cyclamen aldehyde, Diketone, Diol, Doebner reaction, Doebner–Miller reaction, E1cB-elimination reaction, Enone, Favorskii reaction, Fenestrane, Glutaraldehyde, Griseofulvin, Guerbet reaction, Helional, Hexabenzocoronene, Hexyl cinnamaldehyde, Hydroxyacetone, Idose, ..., Ionone, Isophorone, Ivan Ostromislensky, Ketosis, Knoevenagel condensation, Kostanecki acylation, Kröhnke pyridine synthesis, Lilial, List of organic reactions, Lupinine, Macrophomic acid, Malate synthase, Meerwein–Ponndorf–Verley reduction, Mesityl oxide, Mesitylene, Metal carbonyl, Methionine, Molindone, Mukaiyama aldol addition, Neuraminic acid, Nicolaou Taxol total synthesis, Nimodipine, Nucleophile, Olivetol, Oppenauer oxidation, Organolithium reagent, Osteolathyrism, Ouabain, Oxo alcohol, P4-t-Bu, Pechmann condensation, Pentanal, Perkin reaction, Phenylacetaldehyde, Piceol, Progesterone, Proline, Rainer Ludwig Claisen, Raspberry ketone, Reactive distillation, Robinson annulation, Salicylaldehyde, Scientific phenomena named after people, Self-condensation, Sodium tetradecyl sulfate, Tetraphenylcyclopentadienone, Trimer (chemistry), Twistane, Vitamin B12 total synthesis, Zinc chloride, 2-Ethyl-1-butanol, 2-Ethylhexanoic acid, 2-Ethylhexanol, 3-Dehydroquinic acid, 3-Deoxy-D-arabino-heptulosonic acid 7-phosphate, 3-Methyl-2-pentanone. Expand index (56 more) »
Acetaldehyde
Acetaldehyde (systematic name ethanal) is an organic chemical compound with the formula CH3CHO, sometimes abbreviated by chemists as MeCHO (Me.
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Acetone
Acetone (systematically named propanone) is the organic compound with the formula (CH3)2CO.
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Acetophenone
Acetophenone is the organic compound with the formula C6H5C(O)CH3 (also represented by the pseudoelement symbols PhAc or BzMe).
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Aconitine
Aconitine is an alkaloid toxin produced by the Aconitum plant, also known as devil's helmet or monkshood.
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Albert Eschenmoser
Albert Eschenmoser (born August 5, 1925) is a Swiss organic chemist best known for his work on the synthesis of complex heterocyclic natural compounds, most notably vitamin B12.
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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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Aldol
An aldol or aldol adduct (from "Aldehyde alcohol") is a hydroxy ketone or aldehyde, and is the product of aldol addition (as opposed to aldol condensation, which produces an α,β-unsaturated carbonyl moiety).
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Aldol reaction
The aldol reaction is a means of forming carbon–carbon bonds in organic chemistry.
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Alexander Dianin
Alexander Pavlovich Dianin (Александр Павлович Дианин; April 20, 1851 – December 6, 1918) was a Russian chemist from Saint Petersburg.
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Auwers synthesis
The Auwers synthesis is a series of organic reactions forming a flavonol from a coumarone.
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Étard reaction
The Étard reaction is a chemical reaction that involves the direct oxidation of an aromatic or heterocyclic bound methyl group to an aldehyde using chromyl chloride.
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Baeyer–Drewson indigo synthesis
The Baeyer–Drewson indigo synthesis (1882) is an organic reaction in which indigo is prepared from 2-nitrobenzaldehyde and acetone The reaction is classified as an aldol condensation.
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Barium hydroxide
Barium hydroxide are chemical compounds with the chemical formula Ba(OH)2(H2O)x.
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Benzaldehyde
Benzaldehyde (C6H5CHO) is an organic compound consisting of a benzene ring with a formyl substituent.
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Benzil
Benzil (systematically known as 1,2-diphenylethane-1,2-dione) is the organic compound with the formula (C6H5CO)2, generally abbreviated (PhCO)2.
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Benzoin condensation
The benzoin condensation is a reaction (often called a condensation reaction, for historical reasons) between two aromatic aldehydes, particularly benzaldehyde.
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Benzylideneacetone
Benzylideneacetone is the organic compound described by the formula C6H5CH.
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Benzyltrimethylammonium hydroxide
Benzyltrimethylammonium hydroxide, also known as Triton B or trimethylbenzylammonium hydroxide, is a quaternary ammonium salt that functions as an organic base.
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Beta-Hydroxy beta-methylbutyric acid
β-Hydroxy β-methylbutyric acid (HMB), otherwise known as its conjugate base,, is a naturally produced substance in humans that is used as a dietary supplement and as an ingredient in certain medical foods that are intended to promote wound healing and provide nutritional support for people with muscle wasting due to cancer or HIV/AIDS.
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Biginelli reaction
The Biginelli reaction is a multiple-component chemical reaction that creates 3,4-dihydropyrimidin-2(1H)-ones 4 from ethyl acetoacetate 1, an aryl aldehyde (such as benzaldehyde 2), and urea 3.
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Biosynthesis of doxorubicin
Doxorubicin (DXR) is a 14-hydroxylated version of daunorubicin, the immediate precursor of DXR in its biosynthetic pathway.
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Capnellene
Capnellene is a naturally occurring hydrocarbon derived from Capnella imbricata, a species of soft coral found in Indonesia.
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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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Chalcone
Chalcone is an aromatic ketone and an enone that forms the central core for a variety of important biological compounds, which are known collectively as chalcones or chalconoids.
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Chichibabin pyridine synthesis
The Chichibabin pyridine synthesis is a method for synthesizing pyridine rings.
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Cholesterol total synthesis
Cholesterol total synthesis in chemistry describes the total synthesis of the complex biomolecule cholesterol and is considered a great scientific achievement.
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Cinnamaldehyde
Cinnamaldehyde is an organic compound with the formula C6H5CH.
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Cinnamic acid
Cinnamic acid is an organic compound with the formula C6H5CHCHCO2H.
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Citrate synthase
The enzyme citrate synthase E.C. 2.3.3.1 (previously 4.1.3.7) exists in nearly all living cells and stands as a pace-making enzyme in the first step of the citric acid cycle (or Krebs cycle).
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Citric acid cycle
The citric acid cycle (CAC) – also known as the tricarboxylic acid (TCA) cycle or the Krebs cycle – is a series of chemical reactions used by all aerobic organisms to release stored energy through the oxidation of acetyl-CoA derived from carbohydrates, fats, and proteins into carbon dioxide and chemical energy in the form of adenosine triphosphate (ATP).
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Claisen condensation
The Claisen condensation is a carbon–carbon bond forming reaction that occurs between two esters or one ester and another carbonyl compound in the presence of a strong base, resulting in a β-keto ester or a β-diketone.
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Condensation reaction
A condensation reaction is a class of an organic addition reaction that proceeds in a step-wise fashion to produce the addition product, usually in equilibrium, and a water molecule (hence named condensation).
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Crotonaldehyde
Crotonaldehyde is a chemical compound with the formula CH3CH.
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Cyclamen aldehyde
Cyclamen aldehyde is a fragrance molecule which has been used in soaps, detergents, lotions and perfumes since the 1920s.
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Diketone
A diketone or dione is a molecule containing two ketone groups.
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Diol
A diol or glycol is a chemical compound containing two hydroxyl groups (−OH groups).
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Doebner reaction
The Doebner reaction is the chemical reaction of an aniline with an aldehyde and pyruvic acid to form quinoline-4-carboxylic acids.
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Doebner–Miller reaction
The Doebner–Miller reaction is the organic reaction of an aniline with α,β-unsaturated carbonyl compounds to form quinolines.
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E1cB-elimination reaction
The E1cB elimination reaction is a type of elimination reaction which occurs under basic conditions, where a particularly poor leaving group (such as -OH or -OR) and an acidic hydrogen eliminate to form an additional bond.
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Enone
An enone, also called an α,β-unsaturated carbonyl, is a type of organic compound consisting of an alkene conjugated to a ketone.
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Favorskii reaction
The Favorskii reaction is the nucleophilic attack of an acetylide on a carbonyl group.In fact this rearrangement is observed when alpha-halogenoketones are reacted with alkoxide bases(RO-) and forms carboxylic acids and/esters.
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Fenestrane
A fenestrane in organic chemistry is a type of chemical compound with a central quaternary carbon atom which serves as a common vertex for four fused carbocycles.
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Glutaraldehyde
Glutaraldehyde, sold under the brandname Cidex and Glutaral among others, is a disinfectant and medication.
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Griseofulvin
Griseofulvin is an antifungal medication used to treat a number of types of dermatophytoses (ringworm).
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Guerbet reaction
The Guerbet reaction, named after Marcel Guerbet (1861–1938), is an organic reaction converting a primary aliphatic alcohol into its β-alkylated dimer alcohol with loss of one equivalent of water.
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Helional
Helional (from heliotropin, from which is it commonly derived) is a chemical compound used as a perfume in soap and laundry detergent.
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Hexabenzocoronene
Hexa-peri-hexabenzocoronene is a polycyclic aromatic hydrocarbon with the molecular formula C42H18.
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Hexyl cinnamaldehyde
Hexyl cinnamaldehyde (hexyl cinnamal) is a common additive in perfume and cosmetic industry as aroma substance.
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Hydroxyacetone
Hydroxyacetone, also known as acetol, is an organic chemical consisting of a primary alcohol substituent on acetone.
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Idose
Idose is a hexose, a six carbon monosaccharide.
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Ionone
The ionones are a series of closely related chemical substances that are part of a group of compounds known as rose ketones, which also includes damascones and damascenones.
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Isophorone
Isophorone is an α,β-unsaturated cyclic ketone.
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Ivan Ostromislensky
Ivan Ivanovich Ostromislensky (Иван Иванович Остромысленский, also Iwan Ostromislensky) (9 September 1880 – 16 January 1939) was a Russian organic chemist.
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Ketosis
Ketosis is a metabolic state in which some of the body's energy supply comes from ketone bodies in the blood, in contrast to a state of glycolysis in which blood glucose provides energy.
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Knoevenagel condensation
The Knoevenagel condensation reaction is an organic reaction named after Emil Knoevenagel.
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Kostanecki acylation
The Kostanecki acylation is a method used in organic synthesis to form chromones or coumarins by acylation of O-hydroxyaryl ketones with aliphatic acid anhydrides, followed by cyclization.
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Kröhnke pyridine synthesis
The Kröhnke pyridine synthesis is reaction in organic synthesis between α-pyridinium methyl ketone salts and α, β-unsaturated carbonyl compounds used to generate highly functionalized pyridines.
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Lilial
Lilial (a trade name for lily aldehyde, also known as lysmeral) is a chemical compound commonly used as a perfume in cosmetic preparations and laundry powders, often under the name butylphenyl methylpropional.
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List of organic reactions
Well-known reactions and reagents in organic chemistry include.
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Lupinine
Lupinine is a quinolizidine alkaloid present in the genus Lupinus (colloquially referred to as lupins) of the flowering plant family Fabaceae.
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Macrophomic acid
Macrophomic acid is a fungal metabolite isolated from the fungus Macrophoma commelinae.
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Malate synthase
In enzymology, a malate synthase is an enzyme that catalyzes the chemical reaction The 3 substrates of this enzyme are acetyl-CoA, H2O, and glyoxylate, whereas its two products are (S)-malate and CoA.
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Meerwein–Ponndorf–Verley reduction
The Meerwein–Ponndorf–Verley (MPV) reduction in organic chemistry is the reduction of ketones and aldehydes to their corresponding alcohols utilizing aluminium alkoxide catalysis in the presence of a sacrificial alcohol.
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Mesityl oxide
Mesityl oxide is a α,β-unsaturated ketone with the formula CH3C(O)CH.
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Mesitylene
Mesitylene or 1,3,5-trimethylbenzene is a derivative of benzene with three methyl substituents positioned symmetrically around the ring.
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Metal carbonyl
Metal carbonyls are coordination complexes of transition metals with carbon monoxide ligands.
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Methionine
Methionine (symbol Met or M) is an essential amino acid in humans.
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Molindone
Molindone, sold under the brand name Moban, is an antipsychotic which is used in the United States in the treatment of schizophrenia.
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Mukaiyama aldol addition
The Mukaiyama aldol addition is an organic reaction and a type of aldol reaction between a silyl enol ether and an aldehyde or formate.
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Neuraminic acid
Neuraminic acid (5-amino-3,5-dideoxy-D-glycero-D-galacto-non-2-ulosonic acid) is a 9-carbon monosaccharide (a nonose), a derivative of a ketononose.
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Nicolaou Taxol total synthesis
The Nicolaou Taxol total synthesis, published by K. C. Nicolaou and his group in 1994 concerns the total synthesis of Taxol.
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Nimodipine
Nimodipine (marketed by Bayer as Nimotop) is a dihydropyridine calcium channel blocker originally developed for the treatment of high blood pressure.
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Nucleophile
Nucleophile is a chemical species that donates an electron pair to an electrophile to form a chemical bond in relation to a reaction.
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Olivetol
Olivetol, also known as 5-pentylresorcinol or 5-pentyl-1,3-benzenediol, is an organic compound found in certain species of lichen; it is also a precursor in various syntheses of tetrahydrocannabinol.
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Oppenauer oxidation
Oppenauer oxidation, named after Rupert Viktor Oppenauer, is a gentle method for selectively oxidizing secondary alcohols to ketones.
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Organolithium reagent
Organolithium reagents are organometallic compounds that contain carbon – lithium bonds.
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Osteolathyrism
Osteolathyrism is a collagen cross-linking deficiency brought on by dietary over-reliance on the seeds of Lathyrus sativus or grass pea, a legume often grown as a famine crop in Asia and East Africa.
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Ouabain
Ouabain or (from Somali waabaayo, "arrow poison" through French ouabaïo) also known as g-strophanthin, is a plant derived toxic substance that was traditionally used as an arrow poison in eastern Africa for both hunting and warfare.
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Oxo alcohol
Oxo alcohols are alcohols that are prepared by adding carbon monoxide (CO) and hydrogen (usually combined together as synthesis gas) to an olefin to obtain an aldehyde using the hydroformylation reaction and then hydrogenating the aldehyde to obtain the alcohol.
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P4-t-Bu
P4-t-Bu is a readily accessible chemical from the group of neutral, peralkylated sterically hindered polyaminophosphazenes, which are extremely strong bases but very weak nucleophiles.
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Pechmann condensation
The Pechmann condensation is a synthesis of coumarins, starting from a phenol and a carboxylic acid or ester containing a β-carbonyl group.
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Pentanal
Pentanal, also called pentanaldehyde or valeraldehyde, is an alkyl aldehyde, molecular formula C5H10O.
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Perkin reaction
The Perkin reaction is an organic reaction developed by English chemist William Henry Perkin that is used to make cinnamic acids.
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Phenylacetaldehyde
Phenylacetaldehyde is an organic compound used in the synthesis of fragrances and polymers.
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Piceol
Piceol is a phenolic compound found in the needles and in mycorrhizal roots of Norway spruces (Picea abies).
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Progesterone
Progesterone (P4) is an endogenous steroid and progestogen sex hormone involved in the menstrual cycle, pregnancy, and embryogenesis of humans and other species.
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Proline
Proline (symbol Pro or P) is a proteinogenic amino acid that is used in the biosynthesis of proteins.
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Rainer Ludwig Claisen
Rainer Ludwig Claisen (14 January 1851 – 5 January 1930) was a German chemist best known for his work with condensations of carbonyls and sigmatropic rearrangements.
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Raspberry ketone
Raspberry ketone is a natural phenolic compound that is the primary aroma compound of red raspberries.
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Reactive distillation
Reactive distillation is a process where the chemical reactor is also the still.
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Robinson annulation
The Robinson annulation is a chemical reaction used in organic chemistry for ring formation.
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Salicylaldehyde
Salicylic aldehyde (2-hydroxybenzaldehyde) is the organic compound with the formula C6H4CHO-2-OH.
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Scientific phenomena named after people
This is a list of scientific phenomena and concepts named after people (eponymous phenomena).
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Self-condensation
Self-condensation is an organic reaction in which a chemical compound containing a carbonyl group acts both as the electrophile and the nucleophile in an aldol condensation.
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Sodium tetradecyl sulfate
Sodium tetradecyl sulfate (STS) is a commonly used synonym for 7-ethyl-2-methyl-4-undecanyl sulfate sodium salt which is anionic surfactant that is the active component of the sclerosant drug Sotradecol.
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Tetraphenylcyclopentadienone
Tetraphenylcyclopentadienone is an organic compound with the formula (C6H5)4C4CO.
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Trimer (chemistry)
In chemistry, a trimer is a molecule or an anion formed by combination or association of three molecules or ions of the same substance.
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Twistane
Twistane (IUPAC name: tricyclodecane) is an organic compound with the formula C10H16.
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Vitamin B12 total synthesis
The total synthesis of the complex biomolecule vitamin B12 was first accomplished by the collaborating research groups of Robert Burns Woodward at Harvard and Albert Eschenmoser at ETH in 1972.
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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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2-Ethyl-1-butanol
2-Ethyl-1-butanol (IUPAC name: 2-ethylbutan-1-ol) is an organic chemical compound.
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2-Ethylhexanoic acid
2-Ethylhexanoic acid is the organic compound with the formula CH3(CH2)3CH(C2H5)CO2H.
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2-Ethylhexanol
2-Ethylhexanol (abbreviated 2-EH) is a branched, eight-carbon chiral alcohol.
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3-Dehydroquinic acid
3-Dehydroquinic acid (DHQ) is the first carbocyclic intermediate of the shikimate pathway.
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3-Deoxy-D-arabino-heptulosonic acid 7-phosphate
3-Deoxy-D-arabino-heptulosonic acid 7-phosphate (DAHP) is a 7-carbon ulonic acid.
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3-Methyl-2-pentanone
3-Methyl-2-pentanone (methyl sec-butyl ketone) is an aliphatic ketone and isomer of 2-hexanone.
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Redirects here:
Aldol Condensation, Claisen-Schmidt condensation, Claisen–Schmidt condensation, Claisen–Schmidt reaction.
References
[1] https://en.wikipedia.org/wiki/Aldol_condensation
