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Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/277

Title: An Efficient Synthesis of Aryloxyphenyl Cyclopropyl Methanone: A New Class of Antimycobacterial Agents
Authors: Dwivedi, Namrata
Tewari, Neetu
Tiwari, V K
Chaturvedi, Vinita
Manju, Y K
Srivastava, A
Giakwad, A
Sinha, S
Tripathi, R P
Keywords: Tuberculosis
Tetrabutylammonium bromide
Phenyl cyclopropyl methanones
Wolf- Kishner reduction
Issue Date: 2005
Citation: Bioorg Med Chem Lett.15, 4526-30 (2005)
Abstract: An efficient, high yield and one pot synthesis of phenyl cyclopropyl methanones on reaction of different aryl alcohols with 4’-fluoro-4-chloro-butyrophenone in THF/DMF in presence of NaH /TBAB is reported. All the compounds were evaluated for their antitubercular activities against M. tuberculosis H37 Rv in vitro displaying MICs ranging from 25-3.125 mcg/ml. The most active compounds showed activity against MDR strains and one of them showed marginal enhancement MST in mice.
URI: http://hdl.handle.net/123456789/277
Appears in Collections:Medicinal and Process Chemistry

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