Chemoenzymatic approaches toward dechloroansamitocin P-3

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OriginalspracheEnglisch
Seiten (von - bis)1489-1492
Seitenumfang4
FachzeitschriftOrganic Letters
Jahrgang9
Ausgabenummer8
PublikationsstatusVeröffentlicht - 23 März 2007

Abstract

Equation Presented The enantioselective total synthesis of proansamitocin, a key biosynthetic intermediate of the highly potent antitumor agent ansamitocin P-3, is described which bears a diene-ene RCM as the key macrocyclization step. Feeding of proansamitocin to an AHBA block mutant Actinosynnema pretiosum (HGF073) yielded ansamitocin P-3 as well as dechloroansamitocin P-3, the latter also being formed upon fermentation in the presence of 3-amino-5-methoxybenzoic acid.

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Chemoenzymatic approaches toward dechloroansamitocin P-3. / Meyer, Axel; Brünjes, Marco; Taft, Florian et al.
in: Organic Letters, Jahrgang 9, Nr. 8, 23.03.2007, S. 1489-1492.

Publikation: Beitrag in FachzeitschriftArtikelForschungPeer-Review

Meyer, A, Brünjes, M, Taft, F, Frenzel, T, Sasse, F & Kirschning, A 2007, 'Chemoenzymatic approaches toward dechloroansamitocin P-3', Organic Letters, Jg. 9, Nr. 8, S. 1489-1492. https://doi.org/10.1021/ol0702270
Meyer, A., Brünjes, M., Taft, F., Frenzel, T., Sasse, F., & Kirschning, A. (2007). Chemoenzymatic approaches toward dechloroansamitocin P-3. Organic Letters, 9(8), 1489-1492. https://doi.org/10.1021/ol0702270
Meyer A, Brünjes M, Taft F, Frenzel T, Sasse F, Kirschning A. Chemoenzymatic approaches toward dechloroansamitocin P-3. Organic Letters. 2007 Mär 23;9(8):1489-1492. doi: 10.1021/ol0702270
Meyer, Axel ; Brünjes, Marco ; Taft, Florian et al. / Chemoenzymatic approaches toward dechloroansamitocin P-3. in: Organic Letters. 2007 ; Jahrgang 9, Nr. 8. S. 1489-1492.
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AU - Frenzel, Thomas

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AU - Kirschning, Andreas

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