A stereoselective synthesis of the C1–C9 fragment of (–)-dictyostatin has been achieved by use of a titanium(IV) chloride mediated chelation-controlled Mukaiyama aldol reaction and two modified Horner–Wadsworth–Emmons olefinations (Roush– Masamune and Still–Gennari).

A Practical Synthesis of the C1-C9 Fragment of Dictyostatin / C. Zanato, L.L. Pignataro, Z. Hao, C.M.A. Gennari. - In: SYNTHESIS. - ISSN 0039-7881. - 2008:14(2008), pp. C00408SS.2158-C00408SS.2162.

A Practical Synthesis of the C1-C9 Fragment of Dictyostatin

C. Zanato
Primo
;
L.L. Pignataro
Secondo
;
C.M.A. Gennari
Ultimo
2008

Abstract

A stereoselective synthesis of the C1–C9 fragment of (–)-dictyostatin has been achieved by use of a titanium(IV) chloride mediated chelation-controlled Mukaiyama aldol reaction and two modified Horner–Wadsworth–Emmons olefinations (Roush– Masamune and Still–Gennari).
Aldol reactions; Antitumor agents; Olefination; Stereoselective synthesis; Titanium
Settore CHIM/06 - Chimica Organica
2008
Article (author)
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/56650
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