Tetrafibricin: synthesis of the C1-C13, C15-C25, and C27-C40 fragments

Organic Letters
Samir BouzBouz, Janine Cossy

Abstract

[structure: see text] A sequence of chemoselective cross-metathesis reactions and enantioselective allyltitanations of aldehydes has been used to prepare the C1-C13, C15-C26, and C27-C40 fragments of tetrafibricin.

References

Nov 13, 1992·Journal of Medicinal Chemistry·L AligT Weller
Jan 3, 2003·Organic Letters·Yoshihisa KobayashiYoshito Kishi
Jan 23, 2004·Organic & Biomolecular Chemistry·Amir H HoveydaJoseph P A Harrity

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Citations

Jan 26, 2007·Organic Letters·Ricardo Lira, William R Roush
Nov 20, 2015·Organic Letters·Keisuke NishikawaYoshiki Morimoto
Feb 16, 2018·Angewandte Chemie·Shang-Zheng Sun, Ruben Martin
Mar 12, 2015·Organic & Biomolecular Chemistry·J CornilJ Cossy
Jul 24, 2010·Collection of Czechoslovak Chemical Communications·Venugopal GudipatiDennis P Curran
May 16, 2020·Natural Product Reports·Ryan M Friedrich, Gregory K Friestad
Nov 5, 2020·Chemical Communications : Chem Comm·Ze-Jian XueGuo-Qiang Lin
May 24, 2011·Tetrahedron Letters·Venugopal Gudipati, Dennis P Curran
Oct 14, 2010·Organic Letters·Gregory K Friestad, Gopeekrishnan Sreenilayam
Mar 28, 2013·Journal of the American Chemical Society·Philippe Nuhant, William R Roush
Jan 16, 2014·Organic Letters·Takahiko ItohMichael J Krische

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