Mechanism and Application of Baker–Venkataraman O→C Acyl Migration Reactions

Dana Ameen; Timothy J. Snape

doi:10.1055/s-0034-1379498

Synthesis, Inhaltsverzeichnis

Synthesis 2015; 47(02): 141-158
DOI: 10.1055/s-0034-1379498

review

Mechanism and Application of Baker–Venkataraman O→C Acyl Migration Reactions

Dana Ameen

School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Maudland Building, Preston, Lancashire, PR1 2HE, UK eMail: tjsnape@uclan.ac.uk

,

Timothy J. Snape*

School of Pharmacy and Biomedical Sciences, University of Central Lancashire, Maudland Building, Preston, Lancashire, PR1 2HE, UK eMail: tjsnape@uclan.ac.uk

› Institutsangaben

Abstract

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Abstract

This literature review focuses on the O→C acyl migration of aryl esters to yield the corresponding 1,3-dicarbonyl products—a reaction known as the Baker–Venkataraman rearrangement—and outlines their subsequent transformations. The purpose of the review is to highlight the utility of the rearrangement which provides a key step in the synthesis of various heterocyclic motifs. The scope of the Baker–Venkataraman rearrangement is illustrated by way of numerous examples of its application, and in doing so, the review contains over 100 references and covers just over 100 years of the literature, from the first report of the rearrangement by Auwers in 1910 up to more recent examples in the past few years.

1 Introduction

2 Historical Perspective

3 Mechanism

4 Applications: General Routes to Heterocycles

4.1 Flavones and Flavanones

4.2 Xanthones

4.3 Chromones

4.4 Coumarins

4.5 Anthrapyran and Anthracyclin Antibiotics

4.6 Benzopyrans

5 The Retro-Baker–Venkataraman Rearrangement

6 Summary and Outlook

Key words

acyl migrations - rearrangements - Baker–Venkataraman - heterocycles - aryl esters

Volltext

Referenzen

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