Synthesis and reactivity of propargylamines in organic chemistry

K Lauder, A Toscani, N Scalacci… - Chemical reviews, 2017 - ACS Publications
Propargylamines are a versatile class of compounds which find broad application in many
fields of chemistry. This review aims to describe the different strategies developed so far for …

Acetylcholinesterase and carbonic anhydrase inhibitory properties of novel urea and sulfamide derivatives incorporating dopaminergic 2-aminotetralin scaffolds

B Özgeriş, S Göksu, LP Köse, I Gülçin… - Bioorganic & medicinal …, 2016 - Elsevier
In the present study a series of urea and sulfamide compounds incorporating the tetralin
scaffolds were synthesized and evaluated for their acetylcholinesterase (AChE), human …

Discovery of potent carbonic anhydrase and acetylcholine esterase inhibitors: Novel sulfamoylcarbamates and sulfamides derived from acetophenones

A Akıncıoğlu, H Akıncıoğlu, İ Gülçin, S Durdagi… - Bioorganic & medicinal …, 2015 - Elsevier
In this study, several novel sulfamides were synthesized and evaluated for their
acetylcholine esterase (AChE) and human carbonic anhydrase I, and II isoenzymes (hCA I …

A review towards synthesis of heterocycles using propargyl alcohols and propargyl amines

AR Pandey, DK Tiwari, A Prakhar, DP Mishra… - Monatshefte für Chemie …, 2022 - Springer
In the area of drug discovery, nitrogen/oxygen-based heterocycles have been utilized as key
intermediates and have great attention in organic chemistry. A literature survey reveals that …

The human carbonic anhydrase isoenzymes I and II (hCA I and II) inhibition effects of trimethoxyindane derivatives

P Taslimi, I Gulcin, B Ozgeris, S Goksu… - Journal of enzyme …, 2016 - Taylor & Francis
Abstract Carbonic anhydrases (CAs, EC 4.2. 1.1) had six genetically distinct families
described to date in various organisms. There are 16 known CA isoforms in humans. Human …

Acetylcholinesterase inhibitory and antioxidant activities of novel symmetric sulfamides derived from phenethylamines

K Aksu, F Topal, I Gulcin, F Tümer… - Archiv der …, 2015 - Wiley Online Library
The antioxidant and acetylcholinesterase inhibitory properties of novel symmetric sulfamides
derived from phenethylamines were evaluated. Phenethylamines 8–11 were reacted with …

Synthesis and inhibitory properties of some carbamates on carbonic anhydrase and acetylcholine esterase

S Yılmaz, Y Akbaba, B Özgeriş, LP Köse… - Journal of enzyme …, 2016 - Taylor & Francis
A series of carbamate derivatives were synthesized and their carbonic anhydrase I and II
isoenzymes and acetylcholinesterase enzyme (AChE) inhibitory effects were investigated …

Design, synthesis and anticholinergic properties of novel α-benzyl dopamine, tyramine, and phenethylamine derivatives

A Naderi, A Akıncıoğlu, A Çağan, H Çelikkaleli… - Bioorganic …, 2024 - Elsevier
Due to the important biological properties of dopamine, phenethylamine, and tyramine
derivatives in the central nervous system, herein the synthesis of novel α-benzyl dopamine …

Synthesis and anticancer activity of novel ureas and sulfamides incorporating 1-aminotetralins

B Özgeriş, Y Akbaba, Ö Özdemir, H Türkez… - Archives of Medical …, 2017 - Elsevier
Background and Aims In the present study, a series of ureas and sulfamides derived from 1-
aminotetralins were synthesized. For this purpose, urea and sulfamide analogues were …

Synthesis of propargylamine: pioneering a green path with non-conventional KA2 coupling approach

L Khadanga, SM Roopan - Molecular Diversity, 2024 - Springer
The KA 2 coupling reaction is a well-explored and versatile method for forming C–C bonds
in synthetic chemistry. It is composed of ketone, amine, and alkyne, which play a major role …