
Journal of the Chemical Society. Chemical communications p. 2291 - 2292 (1995)
Update date:2022-08-03
Topics:
Hashimura, Kazuya
Tomita, Shun'ichi
Hiroya, Kou
Ogasawara, Kunio
Diastereofacial selectivity in an enantiospecific intramolecular 1,3-dipolar addition is controlled by adjusting the size of the tether between the dipole and the dipolarophile to give 2,3-disubstituted pyrrolidines enantiomeric with respect to the newly
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