Please use this identifier to cite or link to this item:
https://idr.nitk.ac.in/jspui/handle/123456789/12466Full metadata record
| DC Field | Value | Language |
|---|---|---|
| dc.contributor.author | Amrutha, U. | - |
| dc.contributor.author | P.Babu, B. | - |
| dc.contributor.author | Prathapan, S. | - |
| dc.date.accessioned | 2020-03-31T08:39:20Z | - |
| dc.date.available | 2020-03-31T08:39:20Z | - |
| dc.date.issued | 2019 | - |
| dc.identifier.citation | Journal of Heterocyclic Chemistry, 2019, Vol.56, 12, pp.3236-3243 | en_US |
| dc.identifier.uri | http://idr.nitk.ac.in/jspui/handle/123456789/12466 | - |
| dc.description.abstract | In the cycloaddition reaction between fluorenone N-aryl nitrones and 1,1-disubstituted allenes, the initially formed cycloadduct underwent facile [1,3] shift to give 1?-phenylspiro[fluorene-9,2?-pyrrolidin]-4?-ones. Although 1?-phenylspiro[fluorene-9,2?-pyrrolidin]-4?-ones are stable in solid state, a few of them underwent facile aerial oxidation in solution to give the corresponding 1?-phenylspiro[fluorene-9,2?-pyrrolidine]-4?,5?-diones in excellent overall yields. 2019 Wiley Periodicals, Inc. | en_US |
| dc.title | Metal free synthesis of 1-azaspiro[4.4]nonane-3-one system via reactions of nitrones with 1,1-disubstituted allenes | en_US |
| dc.type | Article | en_US |
| Appears in Collections: | 1. Journal Articles | |
Files in This Item:
| File | Description | Size | Format | |
|---|---|---|---|---|
| 2 Metal free synthesis.pdf | 1.05 MB | Adobe PDF |  View/Open |
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