-
practical interest.
Aziridine was
discovered in 1888 by the
chemist Siegmund Gabriel. Its derivatives, also
referred to as
aziridines, are of
broader interest...
- In
organic chemistry,
aziridines are
organic compounds containing the
aziridine functional group (chemical
structure (R−)4C2N−R), a three-membered heterocycle...
-
chemical reaction used in
organic chemistry for the
synthesis of epoxides,
aziridines, and cyclopropanes. It was
discovered in 1961 by A.
William Johnson and...
- pharmaceuticals.
Azomethine ylides can be
generated from many sources,
including aziridines, imines, and iminiums. They are
often generated in situ, and immediately...
-
synthesis is a name
reaction of
organic chemistry, for the
generation of
aziridines from oxiranes. The
oxirane is
first converted into a 2-azidoalcohol with...
- isoindole:
Nitrene cycloaddition. With alkenes,
nitrenes react to form
aziridines, very
often with
nitrenoid precursors such as nosyl- or tosyl-substituted...
-
Chloride Promoted Highly Regioselective Ring
Opening of
Epoxides and
Aziridines Using NaN 3 in Acetonitrile: A
Facile Synthesis of 1,2-Azidoalcohols and...
- (2013-08-20). "Directed Nickel-Catalyzed
Negishi Cross Coupling of
Alkyl Aziridines".
Journal of the
American Chemical Society. 135 (36): 13605–13609. doi:10...
-
unusual conversion of 1-alkyl-2-(bromomethyl)
aziridines into 1-alkyl-2-(N-alkyl-N-ethylaminomethyl)
aziridines using methyllithium Matthias D'hooghe and Norbert...
- many
organic reactions,
including in
alkylations and in the
formation of
aziridines. It is
often a
milder alternative to traditional,
strong inorganic bases...
