- In
organic chemistry,
aziridines are
organic compounds containing the
aziridine functional group (chemical
structure (R−)4C2N−R), a three-membered heterocycle...
-
practical interest.
Aziridine was
discovered in 1888 by the
chemist Siegmund Gabriel. Its derivatives, also
referred to as
aziridines, are of
broader interest...
-
chemical reaction used in
organic chemistry for the
synthesis of epoxides,
aziridines, and cyclopropanes. It was
discovered in 1961 by A.
William Johnson and...
-
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...
- pharmaceuticals.
Azomethine ylides can be
generated from many sources,
including aziridines, imines, and iminiums. They are
often generated in situ, and immediately...
-
Chloride Promoted Highly Regioselective Ring
Opening of
Epoxides and
Aziridines Using NaN 3 in Acetonitrile: A
Facile Synthesis of 1,2-Azidoalcohols and...
-
Aziridiniums are the
ionic form of the
class of
molecules known as
aziridines.
Aziridines can be used to
insert nitrogen atoms during synthesis, but without...
-
unusual conversion of 1-alkyl-2-(bromomethyl)
aziridines into 1-alkyl-2-(N-alkyl-N-ethylaminomethyl)
aziridines using methyllithium Matthias D'hooghe and Norbert...
- R″
groups are
constrained in
cyclic structures such as N-substituted
aziridines (quaternary
ammonium salts are resolvable). In
aromatic amines ("anilines")...
- (2013-08-20). "Directed Nickel-Catalyzed
Negishi Cross Coupling of
Alkyl Aziridines".
Journal of the
American Chemical Society. 135 (36): 13605–13609. doi:10...
