- are two
isomers of
azirine: 1H-
Azirines with a carbon-carbon
double bond are not
stable and
rearrange to the
tautomeric 2H-
azirine, a
compound with a...
-
under UV irradiation,
rearranging to
oxazole through azirine intermediate. Meanwhile, the
azirine intermediate can
react with nucleophiles, especially...
- 41.05 g/mol,
exact m****: 41.0265 u) may
refer to:
Acetonitrile (MeCN)
Azirine Methyl isocyanide, or
isocyanomethane Ethynamine [Wikidata] Ethenimine...
-
Heteroatom Saturated Unsaturated Boron Borirane Borirene Nitrogen Aziridine Azirine Oxygen Oxirane (ethylene oxide, epoxides)
Oxirene Phosphorus Phosphirane...
-
which displaces the
tosylate group in a
nucleophilic displacement to an
azirine and
added water subsequently hydrolyses it to the aminoketone. The Beckmann...
- Volumes, vol. 2, p. 349. Padwa, A.; Blacklock, T.; Tremper, A. "3-Phenyl-2H-
Azirine-2-carboxaldehyde".
Organic Syntheses;
Collected Volumes, vol. 6, p. 893...
-
Azirinomycin is an
antibiotic azirine derivative with the
molecular formula C4H5NO2
which is
produced by the
bacterium Streptomyces aureus. Azirinomycin...
-
Mannich reaction using 2H-
azirines and β-ketoamides. The
racemic 2H-
azirines was
first applied and one
enantiomer of the 2H-
azirine would react with chiral...
-
synthesizing the
starting material. The
mechanism is unknown. However,
azirine intermediates have been isolated. The
mechanism is
postulated to proceed...
- in 1988 in the
marine sponge Dysidea fragilis. Chemically, it is a 2H-
azirine derivative.
Dysidazirine synthesis was
reported for the
first time in 1995...
