- 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...
- 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...
-
alkenes and
aldoximes into nitriles. It can also
cyclize 2-aminoalcohols to
aziridines and to
convert α,β-unsaturated
carboxylic acids to α,β-unsaturated bromides...
- 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...
- The De
Kimpe aziridine synthesis is a name
reaction of
organic chemistry, for the
generation of
aziridines by the
reaction of α-chloroimines with nucleophiles...
- doi:10.1021/ja01314a504. Steuerle, Ulrich; Feuerhake,
Robert (2006). "
Aziridines". Ullmann's
Encyclopedia of
Industrial Chemistry. Weinheim: Wiley-VCH...
