254428-28-9Relevant articles and documents
Reactivity of spiroanthraceneoxazolidines with cyclopropanes: An approach to the oxindole alkaloid scaffold
Buev, Evgeny M.,Moshkin, Vladimir S.,Sosnovskikh, Vyacheslav Y.
supporting information, p. 3409 - 3412 (2018/08/20)
The reaction of N-methylspiro[anthracene-oxazolidine] with spiro[cyclopropane-3,3′-indolin]-2-ones in the presence of MgI2 formed the corresponding spiro[pyrrolidine-3,3′-indolin]-2-ones in 42–65% yields. The use of N-benzylspiro[anthracene-oxazolidine] in this reaction led to the formation of a mixture of the corresponding N-methyl- and N-benzylpyrrolidines.
Facile, novel methodology for the synthesis of spiro[pyrrolidin-3,3'- oxindoles]: Catalyzed ring expansion reactions of cyclopropanes by aldimines
Alper, Phil B.,Meyers, Christiane,Lerchner, Andreas,Siegel, Dionicio R.,Carreira, Erick M.
, p. 3186 - 3189 (2007/10/03)
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