Literature DB >> 1765123

Stereochemistry of enzymic processes in the biosynthesis of pyrrolizidine alkaloids.

D J Robins1.   

Abstract

The harmonization of biosynthetic pathways with organic reaction mechanisms has relied heavily on stereochemical studies. The field of biosynthesis of pyrrolizidine alkaloids exemplifies these connections through a wide range of common organic reactions including oxidation condensation, and decarboxylation. Further, the applications of biogenetic concepts and enzyme-catalysed reactions to synthesis are illustrated. The results are exciting, not only for their intrinsic scientific interest, but because they point the way to using plant enzymes to recognise structurally modified biosynthetic intermediates and hence open routes to the synthesis of new compounds that would otherwise be difficult to obtain.

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Year:  1991        PMID: 1765123     DOI: 10.1007/bf01918375

Source DB:  PubMed          Journal:  Experientia        ISSN: 0014-4754


  4 in total

1.  Studies of enzyme-mediated reactions. Part VI. Stereochemical course of the dehydrogenation of stereospecifically labelled benzylamines by the amine oxidase from pea seedlings (E.C. 1.4.3.6.).

Authors:  A R Battersby; J Staunton; M C Summers
Journal:  J Chem Soc Perkin 1       Date:  1976

Review 2.  The pyrrolizidine alkaloids.

Authors:  D J Robins
Journal:  Fortschr Chem Org Naturst       Date:  1982

Review 3.  Pyrrolizidine alkaloids.

Authors:  D J Robins
Journal:  Nat Prod Rep       Date:  1984-06       Impact factor: 13.423

4.  Synthesis of [3,5-14C]trachelanthamidine and [5-3H]isoretronecanol and their incorporation into the retronecine moiety of riddelliine in Senecio riddellii.

Authors:  E Leete; J Rana
Journal:  J Nat Prod       Date:  1986 Sep-Oct       Impact factor: 4.050

  4 in total

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