Literature DB >> 19675900

Studies towards the total synthesis of lycoposerramine A. Synthesis of a model for the tetracyclic core.

Mark C Elliott1, James S Paine.   

Abstract

Lycoposerramine A (1) is a pentacyclic alkaloid isolated in 2001 by Takayama and co-workers. A concise synthesis of a model compound 8 for the tetracyclic core of this natural product is described. Key steps include the desymmetrising free-radical cyclisation of compound 7 to give compound 18 and spirocyclisation of compound 26 to give compound 8. Earlier approaches using a novel high-yielding stereoselective anionic cyclisation of a cyclohexa-1,4-diene are also reported.

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Year:  2009        PMID: 19675900     DOI: 10.1039/b909860g

Source DB:  PubMed          Journal:  Org Biomol Chem        ISSN: 1477-0520            Impact factor:   3.876


  1 in total

1.  Total synthesis of (+)-sieboldine a: evolution of a pinacol-terminated cyclization strategy.

Authors:  Stephen M Canham; David J France; Larry E Overman
Journal:  J Org Chem       Date:  2012-06-26       Impact factor: 4.354

  1 in total

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