Synthesis of aminomethylated calix[4]resorcinarenes

Author: Matsushita, Y.-ichi; Matsui, T.

Description: Aminomethylation at the ortho position with respect to hydroxyl groups of calix[4]resorcinarenes, resorcinol-aldehyde cyclotetramers, was achieved by the Mannich reaction with formaldehyde and the appropriate amine in an alcoholic solution.

Functionalized calix[4]resorcinarenes bearing substituted aminomethyl groups were synthesized by the Mannich reaction of calix[4]resorcinarene in an alcoholic solution.

Subject Headings: Aminomethylated calix; Mannich reaction

Subject headings:

Publication year: 1993

Journal or book title: Tetrahedron Letters

Volume: 34

Issue: 46

Pages: 7433-7436

Find the full text : https://www.sciencedirect.com/science/article/pii/S0040403900601454

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Type: Journal Article

Serial number: 2303