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  • Baker Venkataraman Rearrangement

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    veerpindhari
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    The Baker-Venkataraman Rearrangement involves the base-induced transfer of an ester acyl group in an o-acylated phenol ester, forming a 1,3-diketone. This reaction proceeds through the formation of an enolate intermediate followed by intramolecular acyl transfer, in a manner related to the Claisen condensation reaction.

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    The Baker-Venkataraman Rearrangement involves the base-induced transfer of an ester acyl group in an o-acylated phenol ester, forming a 1,3-diketone. This reaction proceeds through the formation of an enolate intermediate followed by intramolecular acyl transfer, in a manner related to the Claisen condensation reaction.

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    Attribution Non-Commercial (BY-NC)
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    6 views1 page

    Baker Venkataraman Rearrangement

    Uploaded by

    veerpindhari
    The Baker-Venkataraman Rearrangement involves the base-induced transfer of an ester acyl group in an o-acylated phenol ester, forming a 1,3-diketone. This reaction proceeds through the formation of an enolate intermediate followed by intramolecular acyl transfer, in a manner related to the Claisen condensation reaction.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as PDF, TXT or read online from Scribd
    Flag for inappropriate content
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    Baker-Venkataraman Rearrangement

    The base-induced transfer of the ester acyl group in an o-acylated phenol ester, which leads to a 1,3-diketone. This reaction is related to the Claisen Condensation, and proceeds through the formation of an enolate, followed by intramolecular acyl transfer.

    Mechanism of the Baker-Venkataraman Rearrangement

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