2007
DOI: 10.1016/j.ejmech.2007.01.012
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Synthesis and antibacterial activity of oxazolidinones containing triazolyl group

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Cited by 33 publications
(10 citation statements)
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“…Besides this, it is used as a component of veterinary medicines as well as a photographic developer . Fortunately, in synthetic organic chemistry, rongalite has found the application in installing SO 2 functionality into the organic molecules, which could be valuable precursors for many synthetic transformations viz alkenes could be generated from sulfones by using Ramberg‐Bäcklund as well as Julia olefination reactions which can be used for further functionalization to generate diversity in taxing molecules . Not only this, rongalite is an attractive building block to assemble sultine derivatives which are useful masked dienes partners for Diels‐Alder (DA) reaction to construct intricate molecules which are otherwise challenging or almost impossible by other means .…”
Section: Introductionmentioning
confidence: 99%
“…Besides this, it is used as a component of veterinary medicines as well as a photographic developer . Fortunately, in synthetic organic chemistry, rongalite has found the application in installing SO 2 functionality into the organic molecules, which could be valuable precursors for many synthetic transformations viz alkenes could be generated from sulfones by using Ramberg‐Bäcklund as well as Julia olefination reactions which can be used for further functionalization to generate diversity in taxing molecules . Not only this, rongalite is an attractive building block to assemble sultine derivatives which are useful masked dienes partners for Diels‐Alder (DA) reaction to construct intricate molecules which are otherwise challenging or almost impossible by other means .…”
Section: Introductionmentioning
confidence: 99%
“…The result of in vitro antibacterial activity against a spectrum of resistant and susceptible Gram-positive organisms [ 66 ] clearly shows that all compounds ( Figure 29 ) bearing sulfonyl group have good antibacterial activity. Compound showed more potent antibacterial activity than linezolid and vancomycin.…”
Section: Structure Activity Relationship (Sar) [ 26 mentioning
confidence: 99%
“…General procedure for the preparation of 3a-3i and 3j-3q (Fan et al, 2007;Boos et al, 2006;Girisha et al, 2009) Piperazine derivatives 3a-3i were prepared by the reaction of appropriate substituted sulfonamides (0.01 mol) and…”
Section: Synthesis Of 2a and 2bmentioning
confidence: 99%