| dc.contributor.author | Mohammadi Zeydi, Masoud | en_US |
| dc.contributor.author | Mahmoodi, Nosrat O Allah | en_US |
| dc.contributor.author | Ardeshiri Terogeni, Ghorban | en_US |
| dc.date.accessioned | 1399-07-08T18:17:58Z | fa_IR |
| dc.date.accessioned | 2020-09-29T18:17:58Z | |
| dc.date.available | 1399-07-08T18:17:58Z | fa_IR |
| dc.date.available | 2020-09-29T18:17:58Z | |
| dc.date.issued | 2017-10-01 | en_US |
| dc.date.issued | 1396-07-09 | fa_IR |
| dc.date.submitted | 2017-08-15 | en_US |
| dc.date.submitted | 1396-05-24 | fa_IR |
| dc.identifier.citation | Mohammadi Zeydi, Masoud, Mahmoodi, Nosrat O Allah, Ardeshiri Terogeni, Ghorban. (2017). Sulfonylbis(1,4-phenylene)bissulfamic acid (SPSA): Introduction of an efficient and reusable catalyst for the synthesis of bis(indolyl)methanes. Asian Journal of Green Chemistry, 1(2), 78-88. doi: 10.22631/ajgc.2017.95432.1013 | en_US |
| dc.identifier.issn | 2588-5839 | |
| dc.identifier.issn | 2588-4328 | |
| dc.identifier.uri | https://dx.doi.org/10.22631/ajgc.2017.95432.1013 | |
| dc.identifier.uri | http://www.ajgreenchem.com/article_49782.html | |
| dc.identifier.uri | https://iranjournals.nlai.ir/handle/123456789/40811 | |
| dc.description.abstract | A simple, efficient and convenient route is described for the synthesis of <em>bis</em>-indolyl methanes by using recyclable catalyst sulfonylbis(1,4phenylene)bissulfamic acid (SPSA). In this procedure, we synthesize a <em>bis</em>-indolyl methane derivative <em>via </em>the three component reactions of two equivalent indoles with one equivalent of various aromatic aldehydes in the presence of 10 mol% SBSA as a heterogeneous catalyst under solvent-free conditions at 110 °C for the convinced reaction times (30–60 min). The advantages of this protocol towards the synthesis of <em>bis</em>-indolyl methane derivatives are: I) use of solvent-free conditions, II) inexpensive catalyst, III) using commercially available precursors, d) reusability of SBSA up to several cycles without much loss in reactivity, IV) simple work-up, V) high yields of pure products, VI) short reaction times. The structure of all bis(indolyl)methane derivatives were confirmed by melting point, FT-IR, <sup>1</sup>H NMR spectra and were compared with reliable references.<br /> <br /><br /> | en_US |
| dc.format.extent | 840 | |
| dc.format.mimetype | application/pdf | |
| dc.language | English | |
| dc.language.iso | en_US | |
| dc.publisher | Sami Publishing Company | en_US |
| dc.relation.ispartof | Asian Journal of Green Chemistry | en_US |
| dc.relation.isversionof | https://dx.doi.org/10.22631/ajgc.2017.95432.1013 | |
| dc.subject | Sulfonylbis(1 | en_US |
| dc.subject | 4-phenylene)bissulfamic acid (SPSA) Bis-indolyl methanes Aldehyde Indoles Multi-component reactions | en_US |
| dc.subject | Organic Chemistry | en_US |
| dc.title | Sulfonylbis(1,4-phenylene)bissulfamic acid (SPSA): Introduction of an efficient and reusable catalyst for the synthesis of bis(indolyl)methanes | en_US |
| dc.type | Text | en_US |
| dc.type | Original Research Article | en_US |
| dc.contributor.department | Department of Organic Chemistry, Faculty of Sciences, University of Guilan, Rasht, Iran | en_US |
| dc.contributor.department | Department of Organic Chemistry, Faculty of Sciences, University of Guilan, Rasht, Iran | en_US |
| dc.contributor.department | Department of Organic Chemistry, Faculty of Sciences, University of Guilan, Rasht, Iran | en_US |
| dc.citation.volume | 1 | |
| dc.citation.issue | 2 | |
| dc.citation.spage | 78 | |
| dc.citation.epage | 88 | |
| nlai.contributor.orcid | 0000-0002-0264-5748 | |