N-Acetyl-5-arylalkoxytryptamine Analogs: Probing the Melatonin Receptors for MT1-Selectivity

1,6-Dihydro-2H-indeno[5,4-b]furan Derivatives: Design, Synthesis, and Pharmacological Characterization of a Novel Class of Highly Potent MT2-Selective Agonists

(2011) Tatsuki Koike et al.   JOURNAL OF MEDICINAL CHEMISTRY

Design, synthesis and pharmacological evaluation of novel naphthalenic derivatives as selective MT1 melatoninergic ligands

(2010) Christophe Mésangeau et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Synthesis of substituted N-[3-(3-methoxyphenyl)propyl] amides as highly potent MT2-selective melatonin ligands

(2010) Yueqing Hu et al.   BIOORGANIC & MEDICINAL CHEMISTRY LETTERS

Synthesis and pharmacological evaluation of 1,2,3,4-tetrahydropyrazino[1,2-a]indole and 2-[(phenylmethylamino)methyl]-1H-indole analogues as novel melatoninergic ligands

(2009) Christian Markl et al.   BIOORGANIC & MEDICINAL CHEMISTRY

2-[(2,3-Dihydro-1H-indol-1-yl)methyl]melatonin Analogues: A Novel Class of MT2-Selective Melatonin Receptor Antagonists

(2009) Darius P. Zlotos et al.   JOURNAL OF MEDICINAL CHEMISTRY

Synthesis of 3-phenylnaphthalenic derivatives as new selective MT2 melatoninergic ligands

(2008) Sophie Poissonnier-Durieux et al.   BIOORGANIC & MEDICINAL CHEMISTRY

Selective engineering in O-alkylation of m-cresol with benzyl chloride using liquid–liquid–liquid phase transfer catalysis

(2008) Ganapati D. Yadav et al.   JOURNAL OF MOLECULAR CATALYSIS A-CHEMICAL