C–H functionalization of azines

K Murakami, S Yamada, T Kaneda, K Itami - Chemical Reviews, 2017 - ACS Publications
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 …

A decade update on solvent and catalyst-free neat organic reactions: a step forward towards sustainability

A Sarkar, S Santra, SK Kundu, A Hajra, GV Zyryanov… - Green …, 2016 - pubs.rsc.org
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 …

Recent developments in the synthesis of imidazo [1, 2-a] pyridines

K Pericherla, P Kaswan, K Pandey, A Kumar - Synthesis, 2015 - thieme-connect.com
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 …

Recent advances in the chemistry of conjugated nitrosoalkenes and azoalkenes

SMM Lopes, AL Cardoso, A Lemos… - Chemical …, 2018 - ACS Publications
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 …

Enantioselective dearomatization of indoles by an azoalkene‐enabled (3+ 2) reaction: access to pyrroloindolines

GJ Mei, X Tang, Y Tasdan, Y Lu - Angewandte Chemie, 2020 - Wiley Online Library
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 …

Recent Advances in the Synthesis of Imidazo[1,2‐a]pyridines: A Brief Review

J Panda, BP Raiguru, M Mishra, S Mohapatra… - …, 2022 - Wiley Online Library
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 …

Iodine-catalyzed regioselective thiolation of imidazo [1, 2-a] pyridines using sulfonyl hydrazides as a thiol surrogate

AK Bagdi, S Mitra, M Ghosh, A Hajra - Organic & Biomolecular …, 2015 - pubs.rsc.org
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 …

Medicinal attributes of imidazo [1, 2-a] pyridine derivatives: an update

N Devi, D Singh, RK Rawal, J Bariwal… - Current topics in …, 2016 - ingentaconnect.com
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 …

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 …

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 …