Click Chemistry on Solid Support: Synthesis of a New REM Resin and Application for the Preparation of Tertiary Amines

Löber S, Gmeiner P (2004)

Publication Type: Journal article

Publication year: 2004

Journal

Tetrahedron Elsevier

Publisher: Elsevier

Book Volume: 60

Pages Range: 8699-8702

DOI: 10.1016/j.tet.2004.05.099

Abstract

1,3-Dipolar cycloaddition was employed for the synthesis of a highly practical REM resin. Exploiting this concept, the resulting triazolylmethyl acrylate (TMA) resin was used for an efficient parallel synthesis of tertiary amines by Michael addition, subsequent quarternization and cleavage by means of β-elimination. © 2004 Elsevier Ltd. All rights reserved.

Authors with CRIS profile

Stefan Löber Lehrstuhl für Pharmazeutische Chemie Peter Gmeiner Lehrstuhl für Pharmazeutische Chemie

How to cite

APA:

Löber, S., & Gmeiner, P. (2004). Click Chemistry on Solid Support: Synthesis of a New REM Resin and Application for the Preparation of Tertiary Amines. Tetrahedron, 60, 8699-8702. https://doi.org/10.1016/j.tet.2004.05.099

MLA:

Löber, Stefan, and Peter Gmeiner. "Click Chemistry on Solid Support: Synthesis of a New REM Resin and Application for the Preparation of Tertiary Amines." Tetrahedron 60 (2004): 8699-8702.

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