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Synthesis of novel rhodanine based functionalized furans from the reaction of tert-butyl isocyanide with acetylenic esters in the presence of rhodanine acetic acid derivatives
The reactive 1:1 intermediate produced from the reaction of tert-butyl isocyanide and dialkyl acetylenedicarboxylates was trapped by rhodanine-N-acetic acid derivatives to generate polyfunctionalized furan rings in fairly good yields. The reactive 1:1 intermediate produced from the reaction of tert-...
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Published in: | Arabian journal of chemistry 2019-11, Vol.12 (7), p.1496-1500 |
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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 reactive 1:1 intermediate produced from the reaction of tert-butyl isocyanide and dialkyl acetylenedicarboxylates was trapped by rhodanine-N-acetic acid derivatives to generate polyfunctionalized furan rings in fairly good yields.
The reactive 1:1 intermediate produced from the reaction of tert-butyl isocyanide and dialkyl acetylenedicarboxylates was trapped by rhodanine-N-acetic acid derivatives to generate polyfunctionalized furan rings in fairly good yields. |
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ISSN: | 1878-5352 1878-5379 |
DOI: | 10.1016/j.arabjc.2014.10.030 |