Enantioselective synthesis of cyanohydrins catalysed by hydroxynitrile lyases – a review

Paula Bracco Garcia, Hanna Busch, J. von Langermann, Ulf Hanefeld

Research output: Contribution to journalArticleScientificpeer-review

47 Citations (Scopus)
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Abstract

The first enantioselective synthesis was the selective addition of cyanide to benzaldehyde catalysed by a hydroxynitrile lyase (HNL). Since then these enzymes have developed into a reliable tool in organic synthesis. HNLs to prepare either the (R)- or the (S)-enantiomer of the desired cyanohydrin are available and a wide variety of reaction conditions can be applied. As a result of this, numerous applications of these enzymes in organic synthesis have been described. Here the examples of the last decade are summarised, the enzyme catalysed step is discussed and the follow-up chemistry is shown. This proves HNLs to be part of main stream organic synthesis. Additionally the newest approaches via immobilisation and reaction engineering are introduced.
Original languageEnglish
Number of pages21
JournalOrganic & Biomolecular Chemistry
DOIs
Publication statusPublished - 1 Jun 2016

Keywords

  • Gold for Gold
  • Open Access

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