- In
organic chemistry, the
Menshutkin reaction converts a
tertiary amine into a
quaternary ammonium salt by
reaction with an
alkyl halide.
Similar reactions...
- and nature.
Menshutkin 1952, p. 15.
Menshutkin 1952, p. 16.
Menshutkin 1952, p. 20.
Menshutkin 1952, p. 17.
Menshutkin 1952, p. 23.
Menshutkin 1952, p. 24...
-
Nikolai Aleksandrovich Menshutkin (Russian: Николай Александрович Меншуткин; 24
October [O.S. 12 October] 1842 – 5 February [O.S. 22 January] 1907) was...
-
Hydroamination is
another green method for N-alkylation.[citation needed] In the
Menshutkin reaction, a
tertiary amine is
converted into a
quaternary ammonium salt...
-
tertiary amine the
reaction product is a
quaternary ammonium salt in the
Menshutkin reaction: R 3 − N | R 2 R 1 | : ⏟
tertiary amine + R 4 X ⏟ halogeno- alkane...
-
Graebe (discoverer of alizarin),
Oscar Loew,
Constantin Fahlberg,
Nikolai Menshutkin,
Vladimir Markovnikov (first to
describe carbocycles smaller and larger...
- 87. ISBN 978-1-84212-272-3. As
reported by Sokolov,
quoted in
Boris N.
Menshutkin, Russia's Lomonosov. Chemist, Courtier, Physicist. Princeton, Princeton...
-
tertiary amines by
alkyl halides. This is
often hampered by an
unwanted Menshutkin reaction forming a
quaternary ammonium salt, but is
absent when DIPEA...
- N-alkylation of diazabicyclo[2.2.2]octane (DABCO) with
dichloromethane in a
Menshutkin reaction,
followed by ion
exchange with
sodium tetrafluoroborate (replacing...
-
halides is
widely do****ented. In
older literature this is
often called a
Menshutkin reaction,
however modern chemists usually refer to it
simply as quaternization...
