Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Reactions of Nitrenes with Nucleophiles

7-Azido-nitrobenzoxadiazole (azido-NBD) was observed to undergo a reduction reaction in the absence of an obvious reducing agent, leading to amine formation. In [Pg.218]

Sulfonimidamides lead efficiently to nitrenes and have been converted into sulfimides, sulfoximines, and aziridines in good yields through a copper-mediated [Pg.219]

The diatomic molecule N H and its derivatives R-N are usually referred to as nitrenes, with six electrons on the nitrogen. [Pg.220]

Nitrenes are monovalent nitrogen species, and are isoelectronic with carbenes. Nitrenes like carbenes are immensely reactive and electrophihc. [Pg.220]

The chemistry of nitrenes closely parallels that of carbenes in virtually aU aspects. Like carbenes there is the possibility of two spin states for nitrenes, depending on whether the two nonbonding electrons have their spins paired or parallel. [Pg.220]


See other pages where Reactions of Nitrenes with Nucleophiles is mentioned: [Pg.218]   


SEARCH



Nitrene

Nitrene reactions

Nitrenes

Nitrenes nucleophiles

Nitrenes reactions

Nitrenes reactions, with

Nucleophiles nitrene reactions

Of nitrenes

Reaction with nucleophiles

© 2024 chempedia.info