Literature DB >> 12432496

Thiamin-diphosphate-dependent enzymes: new aspects of asymmetric C-C bond formation.

Martina Pohl1, Bettina Lingen, Michael Müller.   

Abstract

Starting from a thorough investigation of mechanistic aspects of ThDP-dependent (ThDP = thiamin diphosphate) enzymes in combination with mutagenesis studies and a detailed substrate screening, new general synthetic methods have been developed based on Umpolung reactions by thiamin catalysis. A selective donor-acceptor concept was established leading to the first asymmetric cross-benzoin condensation, and a kinetic racemic resolution through C-C bond cleavage was developed. With these tools and in combination with protein engineering, we approached the synthesis of new chiral building blocks on a preparative scale. An outlook is given with respect to the potential of other ThDP-dependent enzymes as catalysts in asymmetric synthesis.

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Year:  2002        PMID: 12432496     DOI: 10.1002/1521-3765(20021202)8:23<5288::AID-CHEM5288>3.0.CO;2-F

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  14 in total

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4.  The Catalytic Asymmetric Intramolecular Stetter Reaction.

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Review 8.  Microbial engineering for aldehyde synthesis.

Authors:  Aditya M Kunjapur; Kristala L J Prather
Journal:  Appl Environ Microbiol       Date:  2015-01-09       Impact factor: 4.792

9.  Nucleophilic carbene catalyzed synthesis of 1,2 amino alcohols via azidation of epoxy aldehydes.

Authors:  Harit U Vora; Johannah R Moncecchi; Oleg Epstein; Tomislav Rovis
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10.  Scope of the asymmetric intramolecular stetter reaction catalyzed by chiral nucleophilic triazolinylidene carbenes.

Authors:  Javier Read de Alaniz; Mark S Kerr; Jennifer L Moore; Tomislav Rovis
Journal:  J Org Chem       Date:  2008-02-27       Impact factor: 4.354

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