Metal free synthesis of 1-azaspiro[4.4]nonane-3-one system via reactions of nitrones with 1,1-disubstituted allenes

dc.contributor.authorAmrutha, U.
dc.contributor.authorP.Babu, B.
dc.contributor.authorPrathapan, S.
dc.date.accessioned2020-03-31T08:39:20Z
dc.date.available2020-03-31T08:39:20Z
dc.date.issued2019
dc.description.abstractIn 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.citationJournal of Heterocyclic Chemistry, 2019, Vol.56, 12, pp.3236-3243en_US
dc.identifier.urihttps://idr.nitk.ac.in/handle/123456789/12466
dc.titleMetal free synthesis of 1-azaspiro[4.4]nonane-3-one system via reactions of nitrones with 1,1-disubstituted allenesen_US
dc.typeArticleen_US

Files

Original bundle

Now showing 1 - 1 of 1
Thumbnail Image
Name:
2 Metal free synthesis.pdf
Size:
1.03 MB
Format:
Adobe Portable Document Format