Systems biocatalysis: para-alkenylation of unprotected phenols. Issue 22 (13th October 2016)

• Record Type: Journal Article
• Authors: Busto, Eduardo; Gerstmann, Michaela; Tobola, Felix; Dittmann, Edmund; Wiltschi, Birgit; Kroutil, Wolfgang
• Is Part Of: Catalysis science & technology. Volume 6:Issue 22(2016)
• Page Start: 8098
• Page End: 8103
• Publication Date: 2016-10-13
• Subjects: Catalysis -- Periodicals; 541.395
• DOI: 10.1039/c6cy01947a
• Languages: English
• ISSNs: 2044-4753

Abstract

Abstract : Commercially available phenol derivatives were transformed with pyruvate to form a new C–C bond leading to the corresponding para -coumaric acids and only one molecule of water as an innocent side product in buffer. Abstract : Commercially available phenol derivatives were transformed with pyruvate to form a new C–C bond leading to the corresponding para -coumaric acids and only one molecule of water as an innocent side product in buffer. The reaction was catalysed by a biocatalytic system consisting of two enzymatic steps, which were run simultaneously: (i) in the first step catalysed by a tyrosine phenol lyase the C–C coupling of phenol derivatives with pyruvate and ammonia yieldedl -tyrosine derivatives, (ii) which were transformed in the second step to the final product via ammonia elimination catalysed by a tyrosine ammonia lyase. The reactions proceeded with exquisite regio- and stereoselectivity yielding just the para -products with the ( E )-configuration. The method represents an efficient approach for the direct alkenylation of phenols on a preparative scale (up to 0.6 mmol) affording ( E )- para -coumaric acids in excellent isolated yields without requiring chromatographic purification. Co-expression of the involved enzymes in a single host gave access to single catalyst preparation.