Reactions of N-phosphorylated aziridines with dianions derived from ethyl acetoacetate and 1,3-diketones: New route to substituted pyrrolines and pyrrolidines

Article abstract of DOI:10.1080/00397919808005953

The nucleophilic ring-opening of N-(diethoxyphosphoryl)aziridines by the dianions derived from ethyl acetoacetate and 1,3-diketones has been studied. Acid-mediated cyclisation and dephosphorylation of the resulting products to a number of substituted pyrrolines and pyrrolidines has been also investigated.

Full text of DOI:10.1080/00397919808005953

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Synthetic Communications: An
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Organic Chemistry
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Reactions of N-Phosphorylated
Aziridines with Dianions
Derived from Ethyl
Acetoacetate and 1,3-
Diketones: New Route to
Substituted Pyrrolines and
Pyrrolidines
a
a
Krystyna Osowska-Pacewicka & Andrzej Zwierzak
a
Institute of Organic Chemistry, Technical University
(Politechnika) , Żwirki 36, Łódź 40, 90-924, Poland
Published online: 15 Aug 2006.
To cite this article: Krystyna Osowska-Pacewicka & Andrzej Zwierzak (1998) Reactions
of N-Phosphorylated Aziridines with Dianions Derived from Ethyl Acetoacetate and
1,3-Diketones: New Route to Substituted Pyrrolines and Pyrrolidines, Synthetic
Communications: An International Journal for Rapid Communication of Synthetic
Organic Chemistry, 28:7, 1127-1137, DOI: 10.1080/00397919808005953
To link to this article: http://dx.doi.org/10.1080/00397919808005953
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