Unprecedented Rearrangement Reaction of 2-Aziridinemethanols with "Lower Order" Lithium Methylcyanocuprate

DOI: 10.1016/S0040-4039(00)60142-9

Source and publish data:

Tetrahedron Letters p. 7421 - 7424 (1993)

Update date:2022-08-05

Topics:

Authors:

Ibuka, Toshiro

Nakai, Kazuo

Habashita, Hiromu

Fujii, Nobutaka

Garrido, Fabrice

et al. et al.

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Article abstract of DOI:10.1016/S0040-4039(00)60142-9

Complementary selectivity can be achieved in ring opening reactions of 2-aziridinemethanols by using either the Gilman reagent or lower order cyanocuprate.In the former case, the usual attack of the Gilman reagent to the substrates 1 and 2 results in the

Full text of DOI:10.1016/S0040-4039(00)60142-9

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