Partial synthesis of a marine secosterol from Gersemia fruticosa: Preparation of the intermediate precursor 3β,6α-diacetoxy-24-methyl-12-oxo-5α-chol-9,11-en-24-oate
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
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1. The applicability of sulfoxide Michael acceptor – 2-(S)-[(4-methylphenyl)sulfinyl]-2-cyclopenten-1-one in constructing the carbon skeleton of 9,11-secosterols;Proceedings of the Estonian Academy of Sciences;2024
2. Towards the total synthesis of 9,11-secosterol: Linking A,B- and D-rings with Michael addition to sulfone-activated cyclopentenone;Tetrahedron;2023-04
3. Designed whole-cell-catalysis-assisted synthesis of 9,11-secosterols;Beilstein Journal of Organic Chemistry;2021-03-01
4. Cnidaria and Ctenophora-2;Encyclopedia of Marine Natural Products;2014-08-07
5. Synthesis of cytotoxic novel 9,11-secosterol analogs: Structure/activity studies;Steroids;2010-12
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