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April 30, 2026
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Novel Formal [3+3] Cycloaddition of Silyl Nitronates with Activated Cyclo­propanes and Its Application in the Synthesis of Pyrroline-N-oxides

Synlett. 2014. Vol. 25. No. 16. P. 2275–2280.
Mikhaylov A. A., Novikov R., Khomutova Y., Arkhipov D., Korlyukov A., Tabolin A., Tomilov Y., Ioffe S.

1,1-Cyclopropane diesters with donor substituents undergo formal [3+3] cycloaddition with various silyl nitronates under Yb(OTf)3 catalysis in the presence of a proton scavenger to give target N-silyloxy tetrahydro-1,2-oxazines in 56–98% yield. The reasons determining the reaction diastereoselectivity are discussed. The resulting tetrahydro-1,2-oxazines are transformed into pyrroline-N-oxides via a novel TfOH-promoted silanol elimination reaction.

Research target: Chemistry
Language: English
DOI
Keywords: donor-acceptor cyclopropanescycloadditionnitro compounds
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