Literature DB >> 11784208

A simple biomimetic synthesis of styelsamine B.

D Skyler1, C H Heathcock.   

Abstract

An extremely rapid, low cost, and environmentally friendly entry into the pyridoacridine family of alkaloids has been devised, as demonstrated here by the first total synthesis of styelsamine B (3) and its oxidation to the quinoneimine cystodytin J (4). The known reaction of cystodytin J with methanethiol makes this a formal synthesis of diplamine. [reaction: see text]

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Year:  2001        PMID: 11784208     DOI: 10.1021/ol010262l

Source DB:  PubMed          Journal:  Org Lett        ISSN: 1523-7052            Impact factor:   6.005


  3 in total

1.  Synthesis, DNA binding and antitumor evaluation of styelsamine and cystodytin analogues.

Authors:  Hugo K H Fong; Brent R Copp
Journal:  Mar Drugs       Date:  2013-01-28       Impact factor: 5.118

Review 2.  New Perspectives in the Chemistry of Marine Pyridoacridine Alkaloids.

Authors:  Alois Plodek; Franz Bracher
Journal:  Mar Drugs       Date:  2016-01-26       Impact factor: 5.118

Review 3.  Pyridinoacridine alkaloids of marine origin: NMR and MS spectral data, synthesis, biosynthesis and biological activity.

Authors:  Louis P Sandjo; Victor Kuete; Maique W Biavatti
Journal:  Beilstein J Org Chem       Date:  2015-09-18       Impact factor: 2.883

  3 in total

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