Dopamine transporter ligands: recent developments and therapeutic potential
SP Runyon, F Carroll - Current topics in medicinal chemistry, 2006 - ingentaconnect.com
The dopamine transporter (DAT) is a target for the development of pharmacotherapies for a
number of central disorders including Parkinson's disease, Alzheimer's disease …
number of central disorders including Parkinson's disease, Alzheimer's disease …
Preclinical evaluation of the abuse potential of Pitolisant, a histamine H3 receptor inverse agonist/antagonist compared with Modafinil
M Uguen, D Perrin, S Belliard… - British journal of …, 2013 - Wiley Online Library
Background and Purpose Pitolisant, a histamine H 3 receptor inverse agonist/antagonist is
currently under P hase III clinical trials for treatment of excessive daytime sleepiness namely …
currently under P hase III clinical trials for treatment of excessive daytime sleepiness namely …
Different routes for the construction of biologically active diversely functionalized bicyclo [3.3. 1] nonanes: an exploration of new perspectives for anticancer …
Cancer is the second most high-morbidity disease throughout the world. From ancient days,
natural products have been known to possess several biological activities, and research on …
natural products have been known to possess several biological activities, and research on …
Biosynthesis of Piperazine-Derived Diazabicyclic Alkaloids Involves a Nonribosomal Peptide Synthetase and Subsequent Tailoring by a Multifunctional Cytochrome …
MT Pham, SR Chen, SY Liang, YB Cheng… - Organic Letters, 2022 - ACS Publications
Piperazine-derived diazabicycles are privileged structures found in natural products and
synthetic chemical entities, including therapeutic agents. Herein, we deciphered the …
synthetic chemical entities, including therapeutic agents. Herein, we deciphered the …
Rh (II)-catalyzed C–H alkylation of benzylamines with unactivated alkenes: the influence of acid on linear and branch selectivity
A Das, N Chatani - Organic Letters, 2021 - ACS Publications
The Rh-catalyzed C–H alkylation of benzylamine derivatives with unactivated 1-alkenes that
proceeds via a picolinamide directing group is reported. The crucial role of an acid additive …
proceeds via a picolinamide directing group is reported. The crucial role of an acid additive …
Rh (I)-and Rh (II)-catalyzed C–H alkylation of benzylamines with alkenes and its application in flow chemistry
A Das, N Chatani - Chemical Science, 2021 - pubs.rsc.org
The Rh-catalyzed C–H alkylation of benzylamines with alkenes using a picolinamide
derivative as a directing group is reported. Both Rh (I) and Rh (II) complexes can be used as …
derivative as a directing group is reported. Both Rh (I) and Rh (II) complexes can be used as …
Further Structure−Activity Relationship Studies on 4-((((3S,6S)-6-Benzhydryltetrahydro-2H-pyran-3-yl)amino)methyl)phenol: Identification of Compounds with Triple …
B Gopishetty, S Hazeldine, S Santra… - Journal of medicinal …, 2011 - ACS Publications
To investigate structural alterations of the lead triple uptake inhibitor molecule, disubstituted
4-((((3 S, 6 S)-6-benzhydryltetrahydro-2 H-pyran-3-yl) amino) methyl) phenol, we have …
4-((((3 S, 6 S)-6-benzhydryltetrahydro-2 H-pyran-3-yl) amino) methyl) phenol, we have …
Facile Assembling of Novel 2, 3, 6, 7, 9-pentaazabicyclo-[3.3. 1] nona-3, 7-diene Derivatives under Microwave and Ultrasound Platforms
HM Al-Matar, KM Dawood, WM Tohamy, MA Shalaby - Molecules, 2019 - mdpi.com
Reactions of a series of 3-oxo-2-arylhydrazonopropanal derivatives with two molar ratio of
ammonium acetate afforded a library of tetrasubstituted 2, 3, 6, 7, 9-pentaazabicyclo [3.3. 1] …
ammonium acetate afforded a library of tetrasubstituted 2, 3, 6, 7, 9-pentaazabicyclo [3.3. 1] …
Synthesis of aza-, oxa-, and thiabicyclo [3.1. 0] hexane heterocycles from a common synthetic intermediate
AR Renslo, H Gao, P Jaishankar… - Organic …, 2005 - ACS Publications
An efficient and stereospecific approach to the synthesis of structurally constrained aza-, oxa-
, and thiabicyclo [3.1. 0] hexane heterocycles has been achieved through application of the …
, and thiabicyclo [3.1. 0] hexane heterocycles has been achieved through application of the …
Synthesis and structure–activity relationship studies of 3-biaryl-8-oxabicyclo [3.2. 1] octane-2-carboxylic acid methyl esters
L Torun, BK Madras, PC Meltzer - Bioorganic & medicinal chemistry, 2012 - Elsevier
Stille cross coupling protocols were utilized for the synthesis of 3-(biaryl)-8-oxabicyclo [3.2.
1] oct-2-ene-2-carboxylic acid methyl esters, which furnished products in high yields where …
1] oct-2-ene-2-carboxylic acid methyl esters, which furnished products in high yields where …