Studies directed toward the synthesis of terreulactone A: Rapid construction of the A, B, C rings Journal Article


Authors: Liu, H.; Siegel, D. R.; Danishefsky, S. J.
Article Title: Studies directed toward the synthesis of terreulactone A: Rapid construction of the A, B, C rings
Abstract: An efficient, rapid synthesis of the A, B, C rings of terreulactone A is described. Key steps in the synthesis include a diastereoselective benzylic acid rearrangement to create the desired quaternary center at C2 and a mild bromolactonization to assemble the lactonic ring A. © 2006 American Chemical Society.
Keywords: chemistry; chemical structure; molecular structure; cyclization; aspergillus; synthesis; biological product; biological products; sesquiterpenes; sesquiterpene; terreulactone a
Journal Title: Organic Letters
Volume: 8
Issue: 3
ISSN: 1523-7060
Publisher: American Chemical Society  
Date Published: 2006-02-02
Start Page: 423
End Page: 425
Language: English
DOI: 10.1021/ol052618p
PUBMED: 16435850
PROVIDER: scopus
DOI/URL:
Notes: --- - "Cited By (since 1996): 16" - "Export Date: 4 June 2012" - "Source: Scopus"
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  1. Haibo Liu
    3 Liu
  2. Dionicio Rhodes Siegel
    4 Siegel