Concept cluster: Chemistry > Organic chemistry reactions
n
(organic chemistry) Reaction with an acetamidomethyl protecting group
n
(organic chemistry) The reaction of a substance with acetic acid or one of its derivatives; the introduction of one or more acetyl groups into a substance.
adj
(organic chemistry) Reacted with acrolein
n
(organic chemistry) Any acyl phosphonite
adj
(organic chemistry) Reacted with, or converted into, an alkyne.
n
(organic chemistry) A product of amidation.
n
(organic chemistry) Reaction with, or formation of an amide
adj
Characteristic of an amide.
n
(organic chemistry) Any cation formed by protonation of an amidine
v
(organic chemistry) To react with, or convert to an amidinium ion
n
(organic chemistry) Any ester of an oxyacid in which one or more -O- linkages are replaced by an -N< (amino) group
n
(organic chemistry) Alternative form of amidium ion [(chemistry) Any cation formed by the addition of a proton to the nitrogen or oxygen atom of an amide or derivative.]
v
(organic chemistry) To introduce one or more amino groups into a compound, in the process of amination
n
(organic chemistry) Any of class of organic radicals, formed by the removal of a hydroxyl group from an amino acid.
n
(organic chemistry) Alternative form of amino aldehyde [(organic chemistry) Any organic compound containing both an amino and an aliphatic aldehyde functional group]
n
(inorganic chemistry) Synonym of Haber process
n
(inorganic chemistry) The univalent NH₄⁺ cation, derived by the protonation of ammonia
adj
(organic chemistry) Modified by the addition of the ring of a cyclic compound, often to form a polycyclic compound
n
(chemistry, archaic) hydrogen peroxide
n
(organic chemistry) Any reaction that results in the formation of an azide
n
(organic chemistry) A peptide that has an azide protecting group on the terminal amine
n
(organic chemistry) Any reaction that results in the formation of an aziridine.
n
(chemistry) A mixture of acetic acid, hydrochloric acid, and acetic anhydride, used as a catalyst for the Beckmann rearrangement.
adj
(organic chemistry) Modified by the addition of, or by cyclization to form, a benzene ring
adj
(organic chemistry) That adds one or more benzyl groups to a molecule
n
(organic chemistry) Reaction with bromoacetic acid or one of its derivatives
n
(organic chemistry) Any reaction in which bromination is accompanied by etherification
n
(organic chemistry) The ring-opening reaction of an bromide with an epoxide
adj
(organic chemistry) Modified by a bromotrifluoromethylation reaction
adj
(organic chemistry) Modified by the addition of a butyrate group
n
(organic chemistry) the introduction of a carbamidomethyl group
v
(organic chemistry) To react with a carbamoyl group
n
(chemistry) the compound HN=C=NH, or any of its hydrocarbyl derivatives
adj
(organic chemistry) That forms a carbonyl group, especially by combination with carbon monoxide
v
(organic chemistry) To react with a carboxamide
n
(organic chemistry) reaction with a carboxyalkyl radical
n
(organic chemistry) reaction with a carboxamide
n
Synonym of carbamidomethylation
n
(organic chemistry) Any reaction that introduces a chloromethyl group into a compound
n
(organic chemistry) Any reaction that introduces a cyanomethyl group
n
(organic chemistry) Reaction with a cyanide (nitrile) group
n
(chemistry) the product of an cycloaddition reaction
n
(organic chemistry) Modification by the addition of, or by cyclization to form, a cyclobutane ring
adj
(organic chemistry) Modified by the addition of, or by cyclization to form, a cyclooctane ring
n
(organic chemistry) Modification by the addition of, or by cyclization to form, a cyclopentane ring.
n
(organic chemistry) Any cyclomer (cyclic polymer) formed from three monomers
adj
(organic chemistry) Describing a compound from which one or more acyl groups has been removed
n
(organic chemistry) Conversion of an amide to a carboxylic acid.
adj
(organic chemistry) That hydrolyses the C-N bond of amides
n
(chemistry) Any reaction that removes bromine from a compound
n
(organic chemistry) Synonym of dediazotation
n
(chemistry) Any reaction in which the elements of hydrogen bromide are removed from a molecule
n
(organic chemistry, in combination) A chemical compound derived by removing a hydroxy group.
n
(organic chemistry) Any reaction that replaces a hydroxyl (-OH) group with fluoride (-F)
adj
(organic chemistry, in combination) From which a methyl group has been removed
n
A photochemical reaction of a molecular entity comprising two p-systems, separated by a saturated carbon atom (a 1,4-diene or an allyl-substituted aromatic analog), to form an ene- (or aryl-) substituted cyclopropane. The rearrangement formally amounts to a 1,2 shift of one ene group (in the diene) or the aryl group (in the allyl-aromatic analog) and ‘bond formation’ between the lateral carbons of the non-migrating moiety.
n
(organic chemistry) Any arylation reaction in which two aryl groups are added to a molecule
n
The intramolecular chemical reaction of diesters with base to give β-ketoesters.
n
(organic chemistry) The cycloaddition reaction between a conjugated diene and an alkene to form a cyclohexene ring.
n
Two molecules of meglumine in a compound
v
(organic chemistry) to undergo the reaction that produces an epoxide; oxidation reactions of alkenes give cyclic ethers in which both carbons of a double bond become bonded to the same oxygen atom)
adj
(organic chemistry) Converted into an epoxide.
adj
(organic chemistry) Having the group CH₃COO-.
n
(organic chemistry) alcoholysis using ethanol
v
(organic chemistry) To react with ethylene oxide
n
(organic chemistry) Any reaction in which a fluoroalkyl group is added to a molecule
n
(organic chemistry) Any reaction that replaces a nitro group with a fluorine atom
n
(organic chemistry) Conversion (especially of an amine) into a guanidine
adj
(organic chemistry) Modified by the addition of seven acyl groups
n
(organic chemistry) treatment or reaction with hydrazine, especially any addition reaction in which the elements of hydrazine are added across a double bond to form a diamine
n
(organic chemistry) A hyperbranched polymer
n
(organic chemistry) Conversion (especially of an amine) into an imide
n
(organic chemistry) copolymer
n
(organic chemistry) Any substitution reaction in which a silane group is replaced by an iodine atom
n
(organic chemistry) An isomer of an imide in which the oxygen and one of the nitrogen atoms are swapped R-N=C(R¹)-O-CO-R
n
(organic chemistry) Any of several classes of lipid, containing amino acid residues, with or without glycerol and/or fatty acid residues, but lacking a phosphate group, that are present in bacteria and similar organisms
n
(inorganic chemistry) The lithium salt of ammonia LiNH₂
adj
(chemistry) Involving many macrocycles
v
(organic chemistry) To add a methoxyl group
adj
(organic chemistry) Containing a methylene group
adj
alkenylated with a single alkene moiety
n
(organic chemistry) Any amidite in which a single -O- linkage is replaced by an -N< (amino) group
adj
(biochemistry) Having a single amino functional group and a single carboxyl or carboxylic acid group.
n
(organic chemistry) Any aminosaccharide that has a single amino group
n
(organic chemistry) Any of various beta-lactam compounds wherein the beta-lactam ring is alone, not fused to another ring.
n
(organic chemistry) Any compound that has a single glycoside unit
n
(organic chemistry) Any compound having a single imine group
n
(organic chemistry, in combination) A single lactyl group in a molecule
n
(organic chemistry) A reaction in which a nitro group is reduced, and often converted into an amino group
n
(organic chemistry) Any reaction with a nitrosyl compound.
adj
(organic chemistry) Having no protecting group
n
(organic chemistry) an ester oligomer chain containing a small number of repeating ester units (monomers). (Oligoesters are short analogs of polymeric polyesters.)
adj
(organic chemistry) Composed of several methylene groups
n
(organic chemistry) Any reaction that forms an oxamide
n
(organic chemistry) Simultaneous oxygenation and iodination
n
(organic chemistry) A linkage between two parts of a molecule by an oxygen atom
n
(organic chemistry, in combination) Five mannosyl groups in a compound
v
(organic chemistry) To modify by perfluoroalkylation
n
(organic chemistry) Any reaction that adds one or more perfluoroalkyl groups to a molecule
n
(organic chemistry) Any reaction in which one or more perfluoroaryl groups are added to a molecule
n
(organic chemistry) Any amidite formally derived from a phosphite; they are used in the synthesis of nucleic acids etc
v
(organic chemistry) To introduce many amine groups into a molecule
n
(organic chemistry, in combination) Many glutamyl groups in a compound
n
(organic chemistry) A compound made up from an odd number of methine groups bound together by alternating single and double bonds.
adj
(chemistry) polycyclic
n
(organic chemistry) Reaction with the triple bond of a propargyl group
n
(organic chemistry) Reaction with a pyridylamino group
n
(organic chemistry) Any reaction in which a tertiary amine is converted to a quaternary ammonium compound
n
(organic chemistry) The conversion of an amine into a quaternary ammonium compound.
n
A quaternary ammonium functional group
v
(organic chemistry) To convert an amine into a quaternary ammonium compound
n
(organic chemistry) The electrophilic alkylation of a nitrile to form an amide
n
(organic chemistry) The conversion of arylamines into aryl halides via diazonium salts
v
(organic chemistry) To react with a squalenoyl group
adj
(organic chemistry) Describing any polymer that has functional groups as its end-groups.
adj
(organic chemistry) That brings about a transnitrosation reaction
n
(organic chemistry) The addition reaction of a trifluoroacetoxy group
n
(organic chemistry) An oligopeptide consisting of three glycine moieties
n
(organic chemistry) The addition of three methyl groups, especially to an amine of a chromatin.
n
(organic chemistry) Reaction with a trinitrophenyl group
n
(chemistry) The synthesis of cis-bicyclo[3.3.0]octane-3,7-dione employing an acetonedicarboxylic acid ester and a diacyl (1,2 ketone); it operates in the same way as the Knoevenagel condensation.

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