Acid hydrazides, potent reagents for synthesis of oxygen-, nitrogen-, and/or sulfur-containing heterocyclic rings

P Majumdar, A Pati, M Patra, RK Behera… - Chemical …, 2014 - ACS Publications
Heterocycles form by far the largest of the classical divisions of organic chemistry. Moreover,
they are of immense importance not only both biologically and industrially but also to the …

Controlled microwave heating in modern organic synthesis: highlights from the 2004–2008 literature

CO Kappe, D Dallinger - Molecular diversity, 2009 - Springer
Direct and rapid heating by microwave irradiation in combination with sealed vessel
processing in many cases enables reactions to be carried out in a fraction of the time …

[图书][B] Microwave heating as a tool for sustainable chemistry

NE Leadbeater - 2010 - taylorfrancis.com
Shorter reaction times, higher product yields, and enhanced selectivity are some of the
advantages microwave heating has over conventional methods, causing its use to transition …

Synthesis and in vitro antitubercular activity of ferrocene-based hydrazones

A Mahajan, L Kremer, S Louw, Y Guéradel… - Bioorganic & medicinal …, 2011 - Elsevier
We report here the synthesis and in vitro antitubercular activity of a new series of ferrocenyl
derivatives. The quinoline-ferrocene hybrid 5 exhibited significant activity (MIC= 2.5–5 …

Palladium-Catalyzed Chemoselective Monoarylation of Hydrazides for the Synthesis of [1,2,4]Triazolo[4,3-a]pyridines

A Reichelt, JR Falsey, RM Rzasa, OR Thiel… - Organic …, 2010 - ACS Publications
An efficient and convenient method for the synthesis of [1, 2, 4] triazolo [4, 3-a] pyridines was
exemplified by the synthesis of 20 analogues bearing a variety of substituents at the 3 …

Recent achievements in the chemistry of 1, 2-diazines

II Mangalagiu - Current Organic Chemistry, 2011 - ingentaconnect.com
Recent studies have centred on 1, 2-diazines derivatives, which proved to be invaluable
materials in the fields of medicine, opto-electronics and agriculture. 1, 2-diazines were found …

Kinase domain inhibition of leucine rich repeat kinase 2 (LRRK2) using a [1, 2, 4] triazolo [4, 3-b] pyridazine scaffold

P Galatsis, JL Henderson, BL Kormos, S Han… - Bioorganic & medicinal …, 2014 - Elsevier
Leucine rich repeat kinase 2 (LRRK2) has been genetically linked to Parkinson's disease
(PD). The most common mutant, G2019S, increases kinase activity, thus LRRK2 kinase …

A Convenient One‐Pot Synthesis of Triazolopyridine and Related Heterocycle Fused‐Triazole Analogs Through Copper Catalyzed Oxidative Cyclization Strategy

R Srinivasan, J Sembian Ruso… - Journal of …, 2016 - Wiley Online Library
One‐pot synthesis of heterocycle fused‐triazole analogs from the corresponding aldehydes
and heteroarylhydrazines is demonstrated. Transformation of hydrazones to the desired …

Discovery and development of a potent and highly selective small molecule muscarinic acetylcholine receptor subtype I (mAChR 1 or M1) antagonist in vitro and in …

CD Weaver, DJ Sheffler, LM Lewis… - Current topics in …, 2009 - ingentaconnect.com
This article describes the discovery and development of the first highly selective, small
molecule antagonist of the muscarinic acetylcholine receptor subtype I (mAChR1 or M1). An …

Five membered ring systems: with more than one N atom

L Yet - Progress in heterocyclic chemistry, 2011 - Elsevier
Publisher Summary This chapter presents the synthesis and chemistry of five-membered
ring system containing more than one nitrogen atom. Diazo, diazonium, and azo compounds …