307495-23-4Relevant academic research and scientific papers
Antimicrobial evaluation of a set of heterobicyclic methylthiadiazole hydrazones: Synthesis, characterization, and SAR studies
Kodisundaram, Paulrasu,Amirthaganesan, Shanmugasundaram,Balasankar, Thirunavukkarasu
, p. 11952 - 11956 (2013)
To exploit the potential antimicrobial activities of azabicyclic skeleton based compounds, a set of 2r,4c-diaryl-3-azabicyclo[3.3.1]nonan-9-one-4-methyl- 1,2,3-thiadazole-5-carbonyl hydrazones were synthesized. Unambiguous structural elucidation has been
Synthesis and antibacterial, antifungal activities of some 2r,4c-diaryl-3-azabicyclo[3.3.1]nonan-9-one-4-aminobenzoyl hydrazones
Xaiver, J. John Francis,Krishnasamy,Sankar
scheme or table, p. 345 - 350 (2012/08/28)
A series of biologically active seven 2r, 4c-diaryl-3-azabicyclo[3.3.1] nonan-9-one-4-aminobenzoyl hydrazone derivatives have been synthesized in good yield. The structures of compounds have been established on the basis of IR, 1H, 13C NMR, and elemental analysis. The structure-activity relationships (SAR) have been studied by screening of antimicrobial activity over a representative panel of bacterial and fungal strains using two-fold serial dilution method. All these synthesized compounds exhibited significant activities against all bacterial and fungal strains. Springer Science+Business Media, LLC 2010.
Synthesis, complete NMR spectral assignments, and antifungal screening of new 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9-one oxime derivatives
Parthiban, Paramasivam,Rathika, Paramasivam,Park, Keun Soo,Jeong, Yeon Tae
experimental part, p. 79 - 93 (2010/07/10)
A series of differently substituted 2,4-diaryl-3-azabicyclo[3.3.1]nonan-9- one oximes have been synthesized and their 1H and 13C NMR chemical shifts have been unambiguously assigned using H,H-COSY, NOESY, HSQC, and HMBC spectral data
