Issue 9, 1990

Perkin communications. Synthesis of 3-amino-4-phenylpyridines: a novel strategy for the preparation of CD ring models of streptonigrin

Abstract

An efficient synthesis of 3-amino-4-phenylpyridine derivatives is reported. 3-Pivaloylaminopyridines were lithiated by butyl-lithium before reaction with iodine as electrophile to afford 4-iodo-3-pivaloylaminopyridines. Cross-coupling of the latter with suitable phenylboronic acids gives CD ring models of streptonigrin.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1990, 2611-2612

Perkin communications. Synthesis of 3-amino-4-phenylpyridines: a novel strategy for the preparation of CD ring models of streptonigrin

F. Marsais, J. Rovera, A. Turck, A. Godard and G. Quéguiner, J. Chem. Soc., Perkin Trans. 1, 1990, 2611 DOI: 10.1039/P19900002611

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Spotlight

Advertisements