Stereoselective synthesis of macrolactin A analogues. Part 1: The C7–C20 fragment
1996; Elsevier BV; Volume: 52; Issue: 36 Linguagem: Inglês
10.1016/0040-4020(96)00666-7
ISSN1464-5416
AutoresThierry Benvegnu, Loı̈c Toupet, R. Grée,
Tópico(s)Cancer Treatment and Pharmacology
ResumoThe tricarbonyliron complexed dienoate 6 corresponding to the C7–C20 fragment of Macrolactin A aromatic analogues was prepared by the aldol reaction of ketone 10 with aldehyde 9, followed by stereoselective reduction.
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