Metal free synthesis of 1-azaspiro[4.4]nonane-3-one system via reactions of nitrones with 1,1-disubstituted allenes
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.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.identifier.citation | Journal of Heterocyclic Chemistry, 2019, Vol.56, 12, pp.3236-3243 | en_US |
dc.identifier.uri | https://idr.nitk.ac.in/handle/123456789/12466 | |
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 |
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