- irradiation,
rearranging to
azirine.
Substituted azirines can be
produced via the
Neber rearrangement.
Photolysis of
azirines (under 300 nm) is a very efficient...
-
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...
-
Heteroatom Saturated Unsaturated Boron Borirane Borirene Nitrogen Aziridine Azirine Oxygen Oxirane (ethylene oxide, epoxides)
Oxirene Phosphorus Phosphirane...
-
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...
-
Albert (1996). "Electronically
Mediated Selectivity in Ring
Opening of 1-
Azirines. The 3-X Mode:
Convenient Route to 3-Oxazolines". The
Journal of Organic...
- 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...
-
electrophilic carbenes to nitriles, by the
photochemical ring
opening of
azirines and by
dehydrochlorination of
imidoyl chlorides. The
latter is the most...
- 1045–1075. doi:10.1039/a909834h. Gilchrist, T. L. (2001). "Activated 2H-
Azirines as
Dienophiles and Electrophiles" (PDF).
Aldrichimica Acta. 34 (2): 51...
-
scheme 2 in an
organic synthesis of oseltamivir:
Certain N-substituted
azirines with
electron withdrawing groups on both
carbons form
azomethine ylides...
