Synthesis of the C1-C16 fragment of the ajudazols

B A Egan, M Paradowski, Lynne H Thomas, R Marquez

Research output: Contribution to journalArticle

12 Citations (Scopus)

Abstract

The synthesis of the C1-C16 framework of the ajudazols has been achieved taking advantage of a highly selective isobenzofuran oxidative rearrangement and a key Stille coupling to introduce the key C14-C15 bond.
Original languageEnglish
Pages (from-to)9700-9707
Number of pages8
JournalTetrahedron
Volume67
Issue number50
DOIs
Publication statusPublished - 16 Dec 2011

Keywords

  • oxidative rearrangement
  • isobenzofuran
  • ajudazol

Cite this

Egan, B. A., Paradowski, M., Thomas, L. H., & Marquez, R. (2011). Synthesis of the C1-C16 fragment of the ajudazols. Tetrahedron, 67(50), 9700-9707. https://doi.org/10.1016/j.tet.2011.10.036

Synthesis of the C1-C16 fragment of the ajudazols. / Egan, B A; Paradowski, M; Thomas, Lynne H; Marquez, R.

In: Tetrahedron, Vol. 67, No. 50, 16.12.2011, p. 9700-9707.

Research output: Contribution to journalArticle

Egan, BA, Paradowski, M, Thomas, LH & Marquez, R 2011, 'Synthesis of the C1-C16 fragment of the ajudazols', Tetrahedron, vol. 67, no. 50, pp. 9700-9707. https://doi.org/10.1016/j.tet.2011.10.036
Egan BA, Paradowski M, Thomas LH, Marquez R. Synthesis of the C1-C16 fragment of the ajudazols. Tetrahedron. 2011 Dec 16;67(50):9700-9707. https://doi.org/10.1016/j.tet.2011.10.036
Egan, B A ; Paradowski, M ; Thomas, Lynne H ; Marquez, R. / Synthesis of the C1-C16 fragment of the ajudazols. In: Tetrahedron. 2011 ; Vol. 67, No. 50. pp. 9700-9707.
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