| Literature DB >> 33078440 |
Christian Paul Bold1, Melanie Gut1, Jasmine Schürmann1, Daniel Lucena-Agell2, Jürg Gertsch3, José Fernando Díaz2, Karl-Heinz Altmann1.
Abstract
We describe the convergent synthesis of three prototypical examples of a new class of analogues of the complex, cytotoxic marine macrolide (-)-zampanolide that incorporate an embedded N-substituted morpholine moiety in place of the natural tetrahydropyran ring. The final construction of the macrolactone core was based on a high-yielding intramolecular HWE olefination, while the hemiaminal-linked side chain was elaborated through a stereoselective, BINAL-H-mediated addition of (Z,E)-sorbamide to a macrocyclic aldehyde precursor. The synthesis of the common functionalized morpholine building block involved two consecutive epoxide openings with tosylamide and the product of the first opening reaction, respectively, as nucleophiles. Of the three morpholino-zampanolides investigated, the N-acetyl and the N-benzoyl derivatives both exhibited nanomolar antiproliferative activity, thus being essentially equipotent with the natural product. In contrast, the activity of the N-tosyl derivative was significantly reduced.Entities:
Keywords: macrocyclization; stereoselective aza aldol reaction; structure-activity relationships; total synthesis; zampanolide
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Year: 2021 PMID: 33078440 DOI: 10.1002/chem.202003996
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236