Synthetic studies toward ansatrienines: Application of the Evans- Tishchenko reaction to chiral enones

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  • Clausthal University of Technology
  • University of Wisconsin
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Original languageEnglish
Pages (from-to)817-820
Number of pages4
JournalTetrahedron Asymmetry
Volume10
Issue number5
Publication statusPublished - 12 Mar 1999
Externally publishedYes

Abstract

Practical syntheses of the C9-C14 sterotriade 5 and the C1-C8 polyene unit 6 in ansatrienine A (mycotriene) (1a), and other ansamycin antibiotics is described. A key step for controlling the configuration of the stereogenic center at C13 involves the stereoselective reduction of enone 10 using the Evans-Tishchenko reaction.

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Synthetic studies toward ansatrienines: Application of the Evans- Tishchenko reaction to chiral enones. / Schöning, Kai Uwe; Hayashi, R. K.; Powell, Douglas R. et al.
In: Tetrahedron Asymmetry, Vol. 10, No. 5, 12.03.1999, p. 817-820.

Research output: Contribution to journalArticleResearchpeer review

Schöning KU, Hayashi RK, Powell DR, Kirschning A. Synthetic studies toward ansatrienines: Application of the Evans- Tishchenko reaction to chiral enones. Tetrahedron Asymmetry. 1999 Mar 12;10(5):817-820. doi: 10.1016/S0957-4166(99)00069-5
Schöning, Kai Uwe ; Hayashi, R. K. ; Powell, Douglas R. et al. / Synthetic studies toward ansatrienines : Application of the Evans- Tishchenko reaction to chiral enones. In: Tetrahedron Asymmetry. 1999 ; Vol. 10, No. 5. pp. 817-820.
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T1 - Synthetic studies toward ansatrienines

T2 - Application of the Evans- Tishchenko reaction to chiral enones

AU - Schöning, Kai Uwe

AU - Hayashi, R. K.

AU - Powell, Douglas R.

AU - Kirschning, Andreas

N1 - Funding information: We thank the Fonds der Chemischen Industrie and the National Science Foundation (grant CHE-9310428) for financial support. Donation of chemicals from E. Merck AG (Darmstadt) is gratefully acknowledged.

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