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Oxalic acid dihydrate and proline based low transition temperature mixture: An efficient synthesis of spiro [diindenopyridine-indoline] triones derivatives
The new facile approach has been developed for the synthesis of spiro [diindenopyridine-indoline] triones under the umbrella of green chemistry. The developed protocol is endowed with the use of low transition temperature mixture as a green reaction medium, operational simplicity, easy workup proced...
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Published in: | Journal of molecular liquids 2016-07, Vol.219, p.573-578 |
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Main Authors: | , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The new facile approach has been developed for the synthesis of spiro [diindenopyridine-indoline] triones under the umbrella of green chemistry. The developed protocol is endowed with the use of low transition temperature mixture as a green reaction medium, operational simplicity, easy workup procedures, good to excellent product yields, and non-chromatographic purification procedure. Since indenone fused motifs have a broad spectrum of biological activities, this protocol is expected to find application in the combinatorial synthesis of biologically active compounds.
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•Low transition temperature mixture (LTTM) as a reaction promoting medium.•100% atom efficient preparation of oxalic acid dihydrate: proline LTTM.•Products with excellent yield, shorter reaction time, high atom economy.•Non-chromatographic purification protocol with mild reaction condition.•Recyclable LTTM. |
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ISSN: | 0167-7322 1873-3166 |
DOI: | 10.1016/j.molliq.2016.02.101 |