2006
DOI: 10.1016/j.bmc.2005.11.025
|View full text |Cite
|
Sign up to set email alerts
|

Efficient microwave enhanced regioselective synthesis of a series of benzimidazolyl/triazolyl spiro [indole-thiazolidinones] as potent antifungal agents and crystal structure of spiro[3H-indole-3,2′-thiazolidine]-3′(1,2,4-triazol-3-yl)-2,4′(1H)-dione

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1

Citation Types

0
65
0
1

Year Published

2006
2006
2017
2017

Publication Types

Select...
7
3

Relationship

1
9

Authors

Journals

citations
Cited by 215 publications
(66 citation statements)
references
References 41 publications
0
65
0
1
Order By: Relevance
“…[4][5][6] The spirooxindole system is the core structure of many pharmacological agents and natural alkaloids. [7][8][9][10] For example, spirotryprostatins A and B, two natural alkaloids isolated from the fermentation broth of Aspergillus fumigatus, have been identified as two novel inhibitors of microtubule assembly, 8) and pteropodine and isopteropodine have been shown to modulate the function of muscarinic serotonin receptors. 10) Xanthene derivatives have been reported to possess diverse biological and therapeutic properties such as antibacterial, antiviral, and anti-inflammatory activities, as well as being useful in photodynamic therapy.…”
mentioning
confidence: 99%
“…[4][5][6] The spirooxindole system is the core structure of many pharmacological agents and natural alkaloids. [7][8][9][10] For example, spirotryprostatins A and B, two natural alkaloids isolated from the fermentation broth of Aspergillus fumigatus, have been identified as two novel inhibitors of microtubule assembly, 8) and pteropodine and isopteropodine have been shown to modulate the function of muscarinic serotonin receptors. 10) Xanthene derivatives have been reported to possess diverse biological and therapeutic properties such as antibacterial, antiviral, and anti-inflammatory activities, as well as being useful in photodynamic therapy.…”
mentioning
confidence: 99%
“…5-Methyl-2,3-diaryl-1,3-thiazolidinones are readily available by use of thiolactic acid in the preparation (Patel et al, 1976) and show antimicrobial activity (Piscopo et al, 1988;Piscopo, Diurno, Gagliardi, Mazzoni, Parrilli & Veneruso, 1989;Piscopo, Diurno, Gagliardi, Mazzoni, De Franceso & Veneruso, 1989;. However, while the crystal structures of a number of 5-methyl-1,3-thiazolidin-4-ones have been reported (Rang et al, 1997;Ö zturk et al, 2000;Dandia et al;2006;Yalçin et al, 2008;Akkurt et al, 2010Akkurt et al, , 2011Akkurt et al, , 2012Ostapiuk et al, 2012;Jiang et al, 2012), only two of them were 2,3-diaryl substituted (Ö zturk et al, 2000;Dandia et al;2006). Herein, we report the synthesis and crystal structure of the cis isomer of rac-5-methyl-2,3-diphenyl-1,3-thiazolidin-4-one.…”
Section: Structure Descriptionmentioning
confidence: 99%
“…These compounds may display pronounced antimicrobial [1], analgesic [2], antiinflammatory [2], antimycobacterial [3], antifungal [4], antitumor [5,6], and antiviral [5,6] activities. Furthermore, 1,3-thiazines are an important type of heterocycles showing also a wide variety of related properties [7 -11].…”
Section: Introductionmentioning
confidence: 99%