Synlett 2018; 29(17): 2218-2224
DOI: 10.1055/s-0037-1610166
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© Georg Thieme Verlag Stuttgart · New York

Synthesis of β-Phenethyl Ethers by Base-Catalyzed Alcohol Addition Reactions to Aryl Alkenes

Chaosheng Luo
Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA   eMail: Jeff.Bandar@colostate.edu
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Department of Chemistry, Colorado State University, Fort Collins, CO 80523, USA   eMail: Jeff.Bandar@colostate.edu
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We thank Colorado State University for the startup funding used to support this work.
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Publikationsverlauf

Received: 17. April 2018

Accepted after revision: 07. Mai 2018

Publikationsdatum:
25. Juni 2018 (online)


Abstract

The direct anti-Markovnikov addition of alcohols to styrene derivatives represents a streamlined route to β-phenethyl ethers, a substructure frequently found in pharmaceuticals and other bioactive ­molecules. Here, we discuss how the development of such a reaction can complement and address limitations of current methods for β-phenethyl ether synthesis. In particular, we highlight our recent ­approach toward achieving this challenging alcohol addition reaction through P4-t-Bu superbase catalysis. A summary of compatible aryl alkenes and alcohols is provided to inform readers of potential applications of this new catalytic transformation, as well as its current limitations and future directions.

1 Introduction

2 Anti-Markovnikov Alcohol Addition to Aryl Alkenes: Background

3 Superbase-Catalyzed Alcohol Addition to Aryl Alkenes

4 Summary and Outlook