C–H functionalization of azines
Azines, which are six-membered aromatic compounds containing one or more nitrogen
atoms, serve as ubiquitous structural cores of aromatic species with important applications in …
atoms, serve as ubiquitous structural cores of aromatic species with important applications in …
A decade update on solvent and catalyst-free neat organic reactions: a step forward towards sustainability
Particular success has been achieved in the synthesis of new products and in processes
since the twelve principles of “green chemistry” were formulated in the 1990s. These …
since the twelve principles of “green chemistry” were formulated in the 1990s. These …
Recent developments in the synthesis of imidazo [1, 2-a] pyridines
Advances in the last decade for the synthesis of the imidazo [1, 2-a] pyridine scaffold from
various substrates employing approaches such as multicomponent reactions, tandem …
various substrates employing approaches such as multicomponent reactions, tandem …
Recent advances in the chemistry of conjugated nitrosoalkenes and azoalkenes
This review aims to present the most recent contributions in the chemistry of nitrosoalkenes
and azoalkenes, highlighting the chemical behavior that makes them important and versatile …
and azoalkenes, highlighting the chemical behavior that makes them important and versatile …
Enantioselective dearomatization of indoles by an azoalkene‐enabled (3+ 2) reaction: access to pyrroloindolines
The enantioselective dearomatization of indoles by an organocatalytic (3+ 2) reaction has
been established. The reaction makes use of simple indole derivatives as substrates, and …
been established. The reaction makes use of simple indole derivatives as substrates, and …
Recent Advances in the Synthesis of Imidazo[1,2‐a]pyridines: A Brief Review
This review focuses on providing comprehensive highlights of the recent synthetic pathways
of imidazo [1, 2‐a] pyridines, assisted through transition metal‐catalyzed reactions, multi …
of imidazo [1, 2‐a] pyridines, assisted through transition metal‐catalyzed reactions, multi …
Iodine-catalyzed regioselective thiolation of imidazo [1, 2-a] pyridines using sulfonyl hydrazides as a thiol surrogate
Iodine-catalyzed regioselective sulfenylation of imidazo [1, 2-a] pyridines via C (sp2)–H
bond functionalization has been achieved using sulfonyl hydrazides as a thiol surrogate. A …
bond functionalization has been achieved using sulfonyl hydrazides as a thiol surrogate. A …
Medicinal attributes of imidazo [1, 2-a] pyridine derivatives: an update
The imidazo [1, 2-a] pyridine scaffold is recognized as a privileged structure as it represents
a promising area for identification of lead structures towards the discovery of new synthetic …
a promising area for identification of lead structures towards the discovery of new synthetic …
Conversion of Pyridine to Imidazo[1,2-a]pyridines by Copper-Catalyzed Aerobic Dehydrogenative Cyclization with Oxime Esters
H Huang, X Ji, X Tang, M Zhang, X Li, H Jiang - Organic letters, 2013 - ACS Publications
Conversion of Pyridine to Imidazo[1,2-a]pyridines by Copper-Catalyzed Aerobic
Dehydrogenative Cyclization with Oxime Esters | Organic Letters ACS ACS Publications C&EN …
Dehydrogenative Cyclization with Oxime Esters | Organic Letters ACS ACS Publications C&EN …
Visible‐Light‐Catalyzed Formal [3+2] Annulation‐Aromatization of Amidines with Isoquinolinium N‐Ylides: Access to Imidazo[2,1‐a]isoquinolines
L Zheng, X Zou, X Yang, L Deng… - Advanced Synthesis & …, 2023 - Wiley Online Library
A visible‐light‐catalyzed formal [3+ 2] annulation‐aromatization reaction for the synthesis of
various substituted imidazo [2, 1‐a] isoquinolines from amidines with stabilized …
various substituted imidazo [2, 1‐a] isoquinolines from amidines with stabilized …