-
Aziridine is an
organic compound consisting of the three-membered
heterocycle C2H5N. It is a colorless, toxic,
volatile liquid that is of significant...
- In
organic chemistry,
aziridines are
organic compounds containing the
aziridine functional group (chemical
structure (R−)4C2N−R), a three-membered heterocycle...
- The Blum–Ittah
aziridine synthesis, also
known as the Blum–Ittah-Shahak
aziridine synthesis or
simply the Blum
aziridine synthesis is a name reaction...
- It can be
viewed as a
structural analog of
aziridine, with
boron replacing the
nitrogen atom of
aziridine.
Borirane is
isomeric with ethylideneborane...
- of an epoxide. Thus,
ethylenimine is the three-membered ring
species aziridine C2H4NH. The
relationship of
imines to
amines having double and single...
-
aziridine with the help of
sulfuric acid. It is used
industrially for the
synthesis of
aziridine itself. The
original Wenker synthesis of
aziridine itself...
- 5-dihydrofuran, coumaran, and dioxane.
Reduction of imines, nitriles, and
aziridines to
primary and
secondary amines traditionally is
effected by
metal hydride...
- C2H5N (molar m****: 43.07 g/mol,
exact m****: 43.0422 u) can
refer to:
Aziridine Ethanimine or its tautomer,
vinylamine N-Methylmethanimine This set index...
-
generation of
aziridines by the
reaction of α-chloroimines with
nucleophiles such as hydride, cyanide, or
Grignard reagents. The De
Kimpe aziridine synthesis...
-
chemical reaction used in
organic chemistry for the
synthesis of epoxides,
aziridines, and cyclopropanes. It was
discovered in 1961 by A.
William Johnson and...
