| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1365702 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
A new series of diarylmethylnapthyloxy ethylamines were synthesized by aminoalkylation of diarylmethylnaphthols which were obtained by Friedel–Crafts alkylation on 1- and 2-naphthols using diarylcarbinols as the alkylating agents. The title compounds were evaluated for antitubercular activity against Mycobacterium tuberculosis H37Rv in vitro and showed MIC in the range of 3.12–25 μg/ml.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Sajal Kumar Das, Gautam Panda, Vinita Chaturvedi, Y.S. Manju, Anil K. Gaikwad, Sudhir Sinha,