Literature DB >> 891762

Lysergylpeptides in the course of peptide ergot alkaloid formation.

A Baumert, D Gröger, W Maier.   

Abstract

Radioactive d-lysergyl-Val-Leu-OMe, d-lysergyl-Val-Val-OMe and d-lysergyl-Val-Val-Pro-OMe were synthetized according to the dicyclohexylcarbodiimide/1-hydroxybenzotriazole procedure. These compounds are not used by intact mycelium of Claviceps as immediate precursors for cyclolalkaloid biosynthesis.

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Year:  1977        PMID： 891762     DOI： 10.1007/bf01951259

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


  5 in total

1.  On the biosynthesis of peptide ergot alkaloids.

Authors:  H G Floss; M Tcheng-Lin; H Kobel; P Stadler
Journal:  Experientia       Date:  1974-12-15

2.  [On the incorporation of dipeptides in ergotoxin alcaloids].

Authors:  D Gröger; S Johne
Journal:  Experientia       Date:  1972-02-15

3.  [A new method for synthesis of peptides: activation of the carboxyl group with dicyclohexylcarbodiimide using 1-hydroxybenzotriazoles as additives].

Authors:  W König; R Geiger
Journal:  Chem Ber       Date:  1970

4.  Biosynthesis of peptide-type ergot alkaloids. Ergotamine.

Authors:  H G Floss; G P Basmadjian; M Tcheng; C Spalla; A Minghetti
Journal:  Lloydia       Date:  1971-12

5.  Biosynthesis of peptide-type ergot alkaloids. Ergocornine and ergocryptine.

Authors:  H G Floss; G P Basmadjian; M Tcheng; D Gröger; D Erge
Journal:  Lloydia       Date:  1971-12
  5 in total

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