adj
(chemistry) Initialism of acid-base. [(chemistry) Relating to or involving interactions between an acid and a base.]
n
(organic chemistry) Any reaction that adds the elements of acetamide to a compound, or creates a derivative of acetamide
n
(organic chemistry) A reaction with an alkoxy group, an alkoxide or an epoxide.
adj
(organic chemistry) Composed of several fused rings
adj
(organic chemistry) That inserts aryl groups into molecules.
n
(organic chemistry) A sulfonylation reaction that uses an arylsulfonyl radical
adj
(organic chemistry) oxygenated in two places
v
(organic chemistry) To form a carboxyl group by introduction of carbon dioxide
adj
(organic chemistry) Describing a tactic polymer in which the double bonds of the repeat units have the cis conformation
adj
Of or pertaining to cycloaddition.
n
(chemistry) Any reaction in which the elements of a hydrogen halide are removed from a molecule.
adj
(organic chemistry) alkylated with two alkyl groups
adj
(organic chemistry, of a pair of substituents) Both in the equatorial configuration
adj
(chemistry) Modified by the addition of two (the same or different) halogen atoms
n
(organic chemistry) The introduction of two hydroxyl groups into a molecule
v
(organic chemistry) To add two methyl groups to a compound
adj
(chemistry) silylated with two silyl groups
n
(organic chemistry) Two substituents in a molecule
v
(organic chemistry) To react so as to form an epoxide
adj
(organic chemistry, of a double bond) Converted into an epoxide by oxidation
n
(organic chemistry) Treatment or reaction with ethylene oxide
adj
(chemistry) Describing an atom or group that is outside the major plane of a molecule (especially of a cyclic molecule)
n
(chemistry) a substitution reaction in which an alkyl or acyl functional group replaces a hydrogen atom of an aromatic nucleus; it is catalyzed by aluminium chloride
n
(organic chemistry, countable) The presence of a functional group.
n
(chemistry) An ionic polymer formed by the reaction of a linear polymer containing carboxylic (or similar) end-groups with divalent metal cations
n
(organic chemistry) Any addition reaction in which a halogen and boron are added across a double bond.
n
(chemistry) The reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst to form a substituted alkene.
n
(organic chemistry) any mono-substituted derivative of hydrogen peroxide - ROOH
adj
(organic chemistry, of a polymer) terminated by a hydroxy group (at one or both ends)
n
(inorganic chemistry) Any giant molecule linked by covalent bonds, but having no (or few) carbon atoms in the main molecular backbone.
n
(chemistry) Any polymer having ionic groups as part of the main chain
n
(organic chemistry) The organic synthesis of cyclopropanols via reaction of esters with dialkyldialkoxytitanium reagents, generated in situ from Grignard reagents bearing hydrogen in beta-position and titanium(IV) alkoxides such as titanium isopropoxide.
n
Denatured ethyl alcohol used as a fuel and a solvent, and usually free of taxes on alcohol. Denaturing is achieved by the addition of methyl alcohol, frequently additional materials are added to give smell and colour to the substance.
n
Alternative spelling of monounsaturate [A monounsaturated oil, or fatty acid]
n
(organic chemistry) The addition of a single acetoxyl group
n
(organic chemistry) acetylation by a single acetyl group
n
(chemistry) Any acid that has only one replaceable hydrogen ion.
n
(organic chemistry) acylation with a single acyl group (where multiple acylations would be possible)
v
(organic chemistry) To introduce a single alkyl group into a molecule
adj
alkylated with a single alkyl group
n
alkylation with a single alkyl group
adj
(organic chemistry) Modified by the addition of a single allyl group
adj
(organic chemistry) arylated by the addition of a single aryl group
n
(organic chemistry) arylation that involves the addition of a single aryl group
n
(chemistry) azidation involving a single azide group
adj
Having a single chelate link
adj
(organic chemistry) Having a single functional group
n
(organic chemistry) modification by the introduction of a single functional group
n
(organic chemistry) The introduction of a single hydroxyl group
n
A single reagent that is a mixture of several others
n
(organic chemistry) saponification of a single ester group
adj
(organic chemistry, of a reaction) That selectively targets a single type of bond or compound
n
(organic chemistry, in combination) A single sialyl group in a molecule
n
(organic chemistry) a substitution reaction that introduces a single substituent into a molecule
adj
(chemistry) That has only one site at which another compound can form a complex
n
(chemistry) The introduction of a single tosyl group into a compound
n
(organic chemistry) The condition of being monounsaturated
adj
(organic chemistry) multiply acetylated
n
(organic chemistry) The conversion of an amine or other compound into a nitroso compound
n
(informal) Alternative form of Orgo [(informal) Organic chemistry.]
n
(organic chemistry) Simultaneous oxygenation and bromination
n
(organic chemistry) cleavage of 1,4 substituents
adj
(organic chemistry) Modified by the addition of one or more polyfluoroalkyl grops
adj
(organic chemistry) Having many hydroxyl substituents.
adj
(organic chemistry) Having many methoxyl groups
n
(chemistry, in combination) Any of various polymers whose respective monomer is a methyl derivative; Any of various compounds having many methyl groups
adj
(chemistry) oxygenated in many parts of the molecule
n
(organic chemistry) The polyimide of succinic acid
adj
(organic chemistry) Treated or coated with a polyurethane varnish or other product.
n
(chemistry) Synonym of Lipinski's rule of five
n
(organic chemistry) A functional group that acts as a sidechain
n
(chemistry) Any part of a molecule, especially a radical
n
(organic chemistry) Any reaction that introduces a thiocarboxylate group into a molecule
n
(organic chemistry) Any reaction that leads to the production of a thioester
adj
(organic chemistry) Modified by the addition of a trialkylstannyl radical
adj
(organic chemistry) Modified by the addition of three methoxyl groups
adj
methylated by the addition of three methyl groups
adj
(organic chemistry) Modified by the addition of three palmitoyl groups
n
(organic chemistry) The addition of a trityl protecting group
n
(chemistry) A set of three rules that invoke the conservation of orbital symmetry to predict the stereochemistry of pericyclic reactions.
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