Iterative amination strategy in the synthesis of peptidomimetics

C.G. Frost; P. Mendonça

doi:10.1246/cl.1997.1159

Iterative amination strategy in the synthesis of peptidomimetics

C.G. Frost, P. Mendonça

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

7 Citations (SciVal)

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
Volume	26
Issue number	11
DOIs	https://doi.org/10.1246/cl.1997.1159
Publication status	Published - 1997

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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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