Coordination behaviour of thiosemicarbazones towards manganese(II) ion

Kanoongo, Neeta; Singh, Rajbir; Tandon, J. P.

doi:10.1002/prac.19883300322

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-(2-phenylthiazol-4-yl)benzonitrile (Iii)1

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1992

2014

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Cited by 6 publications

(3 citation statements)

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“…For the synthesis and bateriostatic activity of indole-3carbaldehyde semithiocarbazone, see: Doyle et al (1956); Fujikawa et al (1966); Libermann et al (1953); Weller et al (1954). For metal complexes of the compound, see: Bhardwaj & Singh (1994); Dalvi et al (2004); Garg & Tandon (1988); Kanoongo et al (1988Kanoongo et al ( , 1990; Kiran et al (1986); Kumari et al (1992a,b;1993a,b); Rodriguez-Argueelles et al (2005); ; Saxena et al (1993; ; Singh et al (1987Singh et al ( , 1988; Varshney & Tandon (1989); Varshney et al ( , 1996. Table 1 Hydrogen-bond geometry (Å , ).…”

Section: Related Literaturementioning

confidence: 99%

1H-Indole-3-carbaldehyde thiosemicarbazone

Razali

Ali

2008

Acta Cryst E

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Section: Related Literaturementioning

confidence: 99%

1H-Indole-3-carbaldehyde thiosemicarbazone

Razali

Ali

2008

Acta Cryst E

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“…This compound has been previously reported . Yield (83%, 0.77 g), white microcrystalline powder, mp: 192–194°C.…”

Section: Methodsmentioning

confidence: 57%

“…1 2-(Thiophen-2-ylmethylene)hydrazinecarbothioamide (Vc). This compound has been previously reported [26,27]. Yield (83%, 0.77 g), white microcrystalline powder, mp: 192-194°C.…”

Section: -(2-phenylthiazol-4-yl)benzonitrile (Iii)mentioning

confidence: 61%

Synthesis and Antimicrobial Evaluation of Some New 4,5′‐Bisthiazoles

Rozsa

Duma

Vlase

et al. 2014

Journal of Heterocyclic Chem

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Thiazole and bisthiazole derivatives represent a prevalent scaffold in the antimicrobial drug discovery. Therefore, we have decided to synthesize some new series of 4,5′‐bisthiazoles. A total of 17 compounds were synthesized, their structural elucidation being based on elemental analysis (C,H,N,S) and spectroscopic data (MS and 1H NMR). Their in vitro antimicrobial activities were assessed against several Gram‐positive and Gram‐negative bacteria strains and also against one fungal strain (Candida albicans) using the difusimetric method. Some of the compounds showed modest to good antibacterial activity against Gram‐negative Escherichia coli and Salmonella typhimurium and Gram‐positive Staphylococcus aureus and Bacillus cereus bacterial strains. All of the synthesized compounds showed moderate to very good antifungal activity against C. albicans.

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