Simple access to spirooxadiazole compounds containing a quinoxaline moiety using a nitrile imine intermediate generated in situ
Abstract: A convenient method for the synthesis of spiro[indeno[1,2-b]quinoxaline-[1,3,4]oxadiazole]s involves a 1,3-dipolar cycloaddition reaction of nitrile imines generated in situ with indenoquinoxaline derivatives.
- Standort
-
Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
-
Online-Ressource
- Sprache
-
Englisch
- Erschienen in
-
Simple access to spirooxadiazole compounds containing a quinoxaline moiety using a nitrile imine intermediate generated in situ ; volume:23 ; number:5 ; year:2017 ; pages:375-378 ; extent:4
Heterocyclic communications ; 23, Heft 5 (2017), 375-378 (gesamt 4)
- Urheber
-
Alizadeh, Abdolali
Moafi, Leila
- DOI
-
10.1515/hc-2017-0084
- URN
-
urn:nbn:de:101:1-2501130635326.519538826032
- Rechteinformation
-
Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
-
15.08.2025, 07:36 MESZ
Datenpartner
Dieses Objekt wird bereitgestellt von:
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Deutsche Nationalbibliothek. Bei Fragen zum Objekt wenden Sie sich bitte an den Datenpartner.
Beteiligte
- Alizadeh, Abdolali
- Moafi, Leila
Ähnliche Objekte (12)
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Reaktive Moleküle mit N-Mehrfachbindungen: Azide, Imine und Nitrile - Synthesen, Pyrolysen, Photoelektronenspektren, quantenchemische Berechnungen
1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Benzophenone Imine
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Moiety modeling framework for deriving moiety abundances from mass spectrometry measured isotopologues
RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
Polyarylene ether nitrile and boron nitride composites: coating with sulfonated polyarylene ether nitrile
Chemisches Verhalten einiger dimolekularen Nitrile
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Reaktive Moleküle mit N-Mehrfachbindungen: Azide, Imine und Nitrile - Synthesen, Pyrolysen, Photoelektronenspektren, quantenchemische Berechnungen
1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Benzophenone Imine
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Moiety modeling framework for deriving moiety abundances from mass spectrometry measured isotopologues
RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
Polyarylene ether nitrile and boron nitride composites: coating with sulfonated polyarylene ether nitrile
Chemisches Verhalten einiger dimolekularen Nitrile
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Ultrafast Dynamics of Photochemical Nitrile Imine Formation
Reaktive Moleküle mit N-Mehrfachbindungen: Azide, Imine und Nitrile - Synthesen, Pyrolysen, Photoelektronenspektren, quantenchemische Berechnungen
1,3-Dipoles: Nitrile Imines, Nitrile Oxides and Nitrile Sulfides
Elucidating the N−N and C−N Bond‐breaking Mechanism in the Photoinduced Formation of Nitrile Imine
Benzophenone Imine
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Glycine Imine—The Elusive α ‐Imino Acid Intermediate in the Reductive Amination of Glyoxylic Acid
Moiety modeling framework for deriving moiety abundances from mass spectrometry measured isotopologues
RuRh Bimetallic Nanoparticles Stabilized by 15-membered Macrocycles-terminated Poly(propylene imine) Dendrimer: Preparation and Catalytic Hydrogenation of Nitrile—Butadiene Rubber
Polyarylene ether nitrile and boron nitride composites: coating with sulfonated polyarylene ether nitrile