A Concise Account of the Chemistry of Valuable Alkyl(methyl)maleic Anhydrides

Prashant S. Deore; Kishan P. Haval; Smita R. Gadre; Narshinha P. Argade

doi:10.1055/s-0034-1378665

Synthesis, Inhaltsverzeichnis

Synthesis 2014; 46(20): 2683-2700
DOI: 10.1055/s-0034-1378665

review

A Concise Account of the Chemistry of Valuable Alkyl(methyl)maleic Anhydrides

Autor*innen

Prashant S. Deore

Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India Fax: +91(20)25902629 eMail: np.argade@ncl.res.in
Kishan P. Haval

Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India Fax: +91(20)25902629 eMail: np.argade@ncl.res.in
Smita R. Gadre

Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India Fax: +91(20)25902629 eMail: np.argade@ncl.res.in
Narshinha P. Argade*

Division of Organic Chemistry, National Chemical Laboratory (CSIR), Pune 411 008, India Fax: +91(20)25902629 eMail: np.argade@ncl.res.in

Abstract

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Abstract

A large number of significant bioactive natural and synthetic alkyl(methyl)maleic anhydrides are known in the contemporary literature. A broad range of suitably functionalized substrates have been tailored to accomplish concise and efficient syntheses of an array of alkyl(methyl)maleic anhydrides employing a variety of elegant synthetic strategies. This review presents a brief literature account of the isolation and activity of these important target compounds with a special emphasis on their synthesis.

1 Introduction

2 Recent Synthetic Strategies towards the Natural and Unnatural Alkyl(methyl)maleic Anhydrides

2.1 Dimethylmaleic Anhydride

2.2 Ethyl/hexyl/octyl(methyl)maleic Anhydrides

2.3 Chaetomellic Anhydrides A–C

2.4 Tyromycin A

2.5 Aspergillus Acids A–D

2.6 Tautomycin and Tautomycetin

2.7 Lindenanolide E, Itaconitin, Graphenone and 2,3-Didehydrotelfairic Anhydride

2.8 Synthetic Analogues of Alkyl(methyl)maleic Anhydrides

3 Summary

Key words

dimethylmaleic anhydride - alkyl(methyl)maleic anhydrides - isolation - bioactivity - nucleophilic reactions - total synthesis

Volltext

Referenzen

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