Literature DB >> 10993348

New pyridone approach: total synthesis of mappicine ketone (nothapodytine B).

K Mekouar1, Y Génisson, S Leue, A E Greene.   

Abstract

A novel synthesis of mappicine ketone, which possesses strong selective activity against the herpes viruses HSV-1 and HSV-2, including those Acyclovir-resistant, and human cytomegalovirus (HCMV) has been efficiently accomplished. The synthesis highlights a new pyridone approach that effectively combines a double, intramolecular Michael addition in a conjugated ester-conjugated amide with oxidation-decarboxylation of the resulting piperidone.

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Year:  2000        PMID: 10993348     DOI: 10.1021/jo0003448

Source DB:  PubMed          Journal:  J Org Chem        ISSN: 0022-3263            Impact factor:   4.354


  1 in total

1.  Directed aromatic functionalization in natural-product synthesis: Fredericamycin A, nothapodytine B, and topopyrones B and D.

Authors:  Charles Dylan Turner; Marco A Ciufolini
Journal:  Beilstein J Org Chem       Date:  2011-10-28       Impact factor: 2.883

  1 in total

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