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Showing 1 to 4 of 4 for “"cis-1,2-Dihydrocatechols"”.

  1. Chemoenzymatic Total Syntheses of Some Biologically Relevant Scaffolds in Homochiral Form

    … compound. Since various enantiomerically pure cis-1,2-dihydrocatechols (such as compounds 3c and 3d) have become available in large quantity via the whole-cell biotransformation of certain halogenated arenes they have become particularly important starting materials in natural product …

    aus-cath Repository record for Chemoenzymatic Total Syntheses of Some Biologically Relevant Scaffolds in Homochiral Form (opens in a new tab)

  2. Chemoenzymatic Total Syntheses of Some Biologically Relevant Scaffolds in Homochiral Form

    … compound. Since various enantiomerically pure cis-1,2-dihydrocatechols (such as compounds 3c and 3d) have become available in large quantity via the whole-cell biotransformation of certain halogenated arenes they have become particularly important starting materials in natural product …

    anu Repository record for Chemoenzymatic Total Syntheses of Some Biologically Relevant Scaffolds in Homochiral Form (opens in a new tab)

  3. Cross-Coupling Chemistry as a Tool for the Synthesis of Diverse Heterocyclic Systems and Natural Products

    … from Enzymatically-derived and Homochiral cis-1,2-Dihydrocatechols' and the last publication is a review article with the title 'Chemical Syntheses of the Cochliomycins and Certain Related Resorcylic Acid Lactones'.

    aus-cath Repository record for Cross-Coupling Chemistry as a Tool for the Synthesis of Diverse Heterocyclic Systems and Natural Products (opens in a new tab)

  4. Cross-Coupling Chemistry as a Tool for the Synthesis of Diverse Heterocyclic Systems and Natural Products

    … from Enzymatically-derived and Homochiral cis-1,2-Dihydrocatechols' and the last publication is a review article with the title 'Chemical Syntheses of the Cochliomycins and Certain Related Resorcylic Acid Lactones'.

    anu Repository record for Cross-Coupling Chemistry as a Tool for the Synthesis of Diverse Heterocyclic Systems and Natural Products (opens in a new tab)