25346-59-2Relevant articles and documents
A new route to trans 2,5-dialkylpyrrolidines
Dumas, Franoise,D'Angelo, Jean
, p. 2005 - 2008 (2007/10/02)
Benzylic amines 8 react with ketoenoates 7 yielding, after reduction of the primary adducts, 2,5-dialkylpyrrolidines 9 (trans isomer predominating). This reaction has been applied to the synthesis of trans 2-heptyl-5-ethylpyrrolidine, a component of the venom of fire ant (Solenopsis punctaticeps).
SYNTHESIS OF FURANS FROM EPOXYCARBONYL PRECURSORS
Cormier, Russell A.,Grosshans, Cheryl A.,Skibbe, Sandra L.
, p. 677 - 680 (2007/10/02)
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