Iterative amination strategy in the synthesis of peptidomimetics

Christopher G. Frost; Paul Mendonça

doi:10.1246/cl.1997.1159

Iterative amination strategy in the synthesis of peptidomimetics

Christopher G. Frost^*, Paul Mendonça

^*Corresponding author for this work

Chemistry

Research output: Contribution to journal › Article › peer-review

7 Citations (Scopus)

Abstract

An iterative palladium catalysed cross-coupling reaction of aryl bromides with amines has been employed in the preparation of novel peptidomimetics. This is a versatile strategy with which we can demonstrate the principle of library synthesis by using a diverse range of coupling partners.

Original language	English
Pages (from-to)	1159-1160
Number of pages	2
Journal	CHEMISTRY LETTERS
Issue number	11
DOIs	https://doi.org/10.1246/cl.1997.1159
Publication status	Published - 1997

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10.1246/cl.1997.1159

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abstract = "An iterative palladium catalysed cross-coupling reaction of aryl bromides with amines has been employed in the preparation of novel peptidomimetics. This is a versatile strategy with which we can demonstrate the principle of library synthesis by using a diverse range of coupling partners.",

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Iterative amination strategy in the synthesis of peptidomimetics

Abstract

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