An
intramolecular force is any force that holds together the atom s making up a molecule or compound They contain all types of chemical
Kaynak: Intramolecular forceThe
intramolecular Heck reaction (IMHR) is the coupling of an aryl or alkenyl halide with an alkene in the same molecule. The reaction may
Kaynak: Intramolecular Heck reactionThe process can also be described as
intramolecular self-assembly, a type of molecular self-assembly , where the molecule is directed to
Kaynak: Folding (chemistry)See also:
intramolecular force s. Image:Triterbutilamin. JPG | The steric effect of tri-(tert- butyl )amine makes electrophilic reactions,
Kaynak: Steric effectsStem-loop
intramolecular base pair ing is a pattern that can occur in single-stranded DNA or, more commonly, in RNA . The structure is
Kaynak: Stem-loopThe Dieckmann condensation is the
intramolecular chemical reaction of diester s with base to give β-ketoesters It is named after the
Kaynak: Dieckmann condensationMacrocyclic stereocontrol refers to the directed outcome of a given intermolecular or
intramolecular reaction on a ring containing 8 or
Kaynak: Macrocyclic stereocontrolThe Bischler–Napieralski reaction is an
intramolecular electrophilic aromatic substitution reaction that allows for the cyclization of β-
Kaynak: Bischler–Napieralski reactionThey are weak compared to the
intramolecular force s, the forces which keep a molecule together. For example, the covalent bond present
Kaynak: Intermolecular forceThe Smiles rearrangement is an organic reaction and a rearrangement reaction It is an
intramolecular nucleophilic aromatic substitution
Kaynak: Smiles rearrangementProtein splicing is an
intramolecular reaction of a particular protein in which an internal protein segment (called an intein ) is removed
Kaynak: Protein splicingThe compound is formed by the
intramolecular nucleophilic addition of a hydroxyl group to the carbonyl group of an aldehyde or a
Kaynak: LactolThe Knorr quinoline synthesis is an
intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using sulfuric
Kaynak: Knorr quinoline synthesisAn NIH shift is a chemical rearrangement where a hydrogen atom on an aromatic ring undergoes an
intramolecular migration primarily during a
Kaynak: NIH shift