Literature DB >> 14601988

A formal construction of fasicularin.

Michaël D B Fenster1, Gregory R Dake.   

Abstract

[reaction: see text] Our synthetic approach toward fasicularin is presented. Key steps in this construction are a siloxy-epoxide semipinacol rearrangement, a B-alkyl Suzuki reaction and an intramolecular S(N)2 reaction.

Entities:  

Year:  2003        PMID： 14601988     DOI： 10.1021/ol035566h

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


  3 in total

Review 1.  Studies on total synthesis of the cylindricine/fasicularin/lepadiformine family of tricyclic marine alkaloids.

Authors:  Steven M Weinreb
Journal:  Chem Rev       Date:  2006-06       Impact factor: 60.622

2.  Aza-[3 + 3] Annulations: A New Unified Strategy in Alkaloid Synthesis.

Authors:  Grant S Buchanan; John B Feltenberger; Richard P Hsung
Journal:  Curr Org Synth       Date:  2010-08-01       Impact factor: 1.975

3.  Diastereoselective functionalisation of benzo-annulated bicyclic sultams: Application for the synthesis of cis-2,4-diarylpyrrolidines.

Authors:  Susan Kelleher; Pierre-Yves Quesne; Paul Evans
Journal:  Beilstein J Org Chem       Date:  2009-11-25       Impact factor: 2.883
  3 in total

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