Stereoselective C-Alkylation of Di-imine Macrocycles: a Versatile Route to a Series of meso-Dialkyl-substituted Macrocyclic Tetramines

DOI: 10.1039/c39830001253

Source and publish data:

Journal of the Chemical Society. Chemical communications p. 1253 - 1254 (1983)

Update date:2022-08-05

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Authors:

Henrick, Kim

Judd, Patricia M.

Owston, Philip G.

Peters, Roger

Tasker, Peter A.

Turner, Ralph W.

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Article abstract of DOI:10.1039/c39830001253

Macrocycles containing two o-iminoanilino units undergo stereoselective C-alkylation on treatment with Grignard reagents or lithium alkyls to give the meso-dialkyl-substituted macrocyclic tetra-amines.

Full text of DOI:10.1039/c39830001253

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