Catalytic asymmetric Michael addition of nitroalkane to enone and enal

DOI: 10.1016/0040-4039(94)88290-8

Source and publish data:

Tetrahedron Letters p. 8233 - 8236 (1994)

Update date:2022-08-03

Topics:

Authors:

Yamaguchi, Masahiko

Shiraishi, Tai

Igarashi, Yoshihiro

Hirama, Masahiro

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Article abstract of DOI:10.1016/0040-4039(94)88290-8

L-Proline rubidium salt catalyzes the asymmetric Michael addition of nitroalkanes to enones and an enal. (R)-Adducts were obtained from cyclic (Z)-enones and (S)-adducts from acyclic (E)-enones, Bu₃SnH treatment of the products replaced the nit

Full text of DOI:10.1016/0040-4039(94)88290-8

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