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Ring expansion and ring contraction reactions expand or contract rings, usually in organic chemistry. The term usually refers to reactions involve making and breaking C-C bonds, [1] Diverse mechanisms lead to these kinds of reactions. The bond migration step of the pinacol type rearrangement.
Buchner ring expansion. The Buchner ring expansion is a two-step organic C-C bond forming reaction used to access 7-membered rings. The first step involves formation of a carbene from ethyl diazoacetate, which cyclopropanates an aromatic ring. The ring expansion occurs in the second step, with an electrocyclic reaction opening the cyclopropane ...
The Büchner ring expansion reactions utilizing diazoalkanes have proven to be synthetically useful as they can not only be used to form 5- and 6-membered rings, but also more unstable 7- and 8-membered rings. The Büchner–Curtius–Schlotterbeck reaction used in one Carbon ring expansions
The Dowd–Beckwith ring-expansion reaction is an organic reaction in which a cyclic carbonyl (typically a β- keto ester) is expanded by up to 4 carbons in a free radical ring expansion reaction through an α-alkylhalo substituent. [1] [2] [3] The radical initiator system is based on AIBN and tributyltin hydride. [ 1]
RXNO:0000381. The Tiffeneau–Demjanov rearrangement ( TDR) is the chemical reaction of a 1-aminomethyl-cycloalkanol with nitrous acid to form an enlarged cycloketone. The Tiffeneau–Demjanov ring expansion, Tiffeneau–Demjanov rearrangement, or TDR, provides an easy way to increase amino-substituted cycloalkanes and cycloalkanols in size by ...
The Demjanov rearrangement is the chemical reaction of primary amines with nitrous acid to give rearranged alcohols. [1] [2] [3] It involves substitution by a hydroxyl group with a possible ring expansion. It is named after the Russian chemist Nikolai Jakovlevich Demjanov (Dem'anov, Demianov), [4] who first reported it in 1903.
The Gabriel–Colman rearrangement [1] is the chemical reaction of a saccharin or phthalimido ester with a strong base, such as an alkoxide, to form substituted isoquinolines. [2] First described in 1900 by chemists Siegmund Gabriel and James Colman, this rearrangement, a ring expansion, is seen to be general if there is an enolizable hydrogen ...
The Buchner ring expansion reaction also involves the formation of a stabilised carbene. Cyclopropanation is also stereospecific as the addition of carbene and carbenoids to alkenes is a form of a cheletropic reaction , with the addition taking place in a syn manner.