Literature DB >> 23773166

Azidation of β-keto esters and silyl enol ethers with a benziodoxole reagent.

Maria Victoria Vita1, Jérôme Waser.   

Abstract

The efficient azidation of β-keto esters and silyl enol ethers using a benziodoxole-derived azide transfer reagent is reported. The azidation of cyclic β-keto esters could be achieved in up to quantitative yields in the absence of any catalyst. In the case of less reactive linear β-keto esters and silyl enol ethers, complete conversion and good yields could be obtained by using a zinc catalyst.

Entities:  

Year:  2013        PMID: 23773166     DOI: 10.1021/ol401229v

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  10 in total

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6.  Three-Component Azidation of Styrene-Type Double Bonds: Light-Switchable Behavior of a Copper Photoredox Catalyst.

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Review 8.  Recent discoveries on the structure of iodine(iii) reagents and their use in cross-nucleophile coupling.

Authors:  Adriano Bauer; Nuno Maulide
Journal:  Chem Sci       Date:  2021-01-07       Impact factor: 9.825

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10.  Towards an Asymmetric Organocatalytic α-Azidation of β-Ketoesters.

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  10 in total

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