Turkish Journal of Chemistry
DOI
10.3906/kim-1408-26
Abstract
A facile one-pot synthesis of novel oxindole derivatives bearing benzothiazolylmethyl-2-thioxothiazolidin-4-one was accomplished via one-pot reaction of 5-oxoindolinylidene rhodanine-3-acetic acid derivatives, 2-aminothiophenol, and triphenyl phosphite in the presence of tetrabutylammonium bromide (TBAB) and nano silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (NSB-DBU) as heterogeneous reusable nanocatalyst. The target compounds were obtained in excellent yields (85%--92%) and short reaction times under fairly mild reaction conditions.
Keywords
Oxindole derivatives, benzothiazoles, 4-thiazolidinones, nano silica-bonded 5-n-propyl-octahydro-pyrimido [1, 2-a]azepinium chloride, nano silica-supported catalyst
First Page
235
Last Page
243
Recommended Citation
BAHARFAR, ROBABEH and SHARIATI, NARGES
(2015)
"Synthesis of new oxindole derivatives containing benzothiazole and thiazolidinone moieties using nano silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (NSB-DBU) as catalyst,"
Turkish Journal of Chemistry: Vol. 39:
No.
2, Article 3.
https://doi.org/10.3906/kim-1408-26
Available at:
https://journals.tubitak.gov.tr/chem/vol39/iss2/3