Comparative<i>S</i>-adenosyl-<scp>l</scp>-methionine analogue generation for selective biocatalytic Friedel-Crafts alkylation-Reference-Cited by-同舟云学术

ComparativeS-adenosyl-l-methionine analogue generation for selective biocatalytic Friedel-Crafts alkylation

Published:2023 Issue:36 Volume:59 Page:5463-5466
ISSN:1359-7345
Container-title:Chemical Communications
language:en
Short-container-title:Chem. Commun.

Author:

Hoffmann Arne¹^ORCID,Schülke Kai H.²^ORCID,Hammer Stephan C.²^ORCID,Rentmeister Andrea¹^ORCID,Cornelissen Nicolas V.¹^ORCID

Affiliation:

1. University of Muenster, Institute of Biochemistry, Corrensstr. 36, Muenster D-48149, Germany

2. Bielefeld University, Faculty of Chemistry, Organic Chemistry and Biocatalysis Universitätsstraße 25, Bielefeld D-33615, Germany

Abstract

Comparison ofS-adenosyl-l-methionine (SAM) analogue generation by halide methyltransferase (HMT) and methionine adenosyltransferase (MAT) for methyltransferase catalysed alkylation.

Funder

Deutsche Forschungsgemeinschaft

Publisher

Royal Society of Chemistry (RSC)

Subject

Materials Chemistry,Metals and Alloys,Surfaces, Coatings and Films,General Chemistry,Ceramics and Composites,Electronic, Optical and Magnetic Materials,Catalysis

Link

http://pubs.rsc.org/en/content/articlepdf/2023/CC/D3CC01036H

Reference28 articles.

1. Profound Methyl Effects in Drug Discovery and a Call for New CH Methylation Reactions

2. Direct transfer of extended groups from synthetic cofactors by DNA methyltransferases

3. Asymmetric β‐Methylation of l ‐ and d ‐α‐Amino Acids by a Self‐Contained Enzyme Cascade

4. S-adenosylhomocysteine as a methyl transfer catalyst in biocatalytic methylation reactions

5. Bioorthogonal Profiling of Protein Methylation Using Azido Derivative of S-Adenosyl-l-methionine

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