Asymmetric synthesis of the 2,2,3-trisubstituted cyclopentanone, D-ring fragment of 9,11-secosterols
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. Synthesis of 2-(S)-[(4-methylphenyl)sulfinyl]-2-cyclopenten-1-one, a D-ring precursor of 9,11-secosterols;Proceedings of the Estonian Academy of Sciences;2022
4. Addition Reactions: Polar Addition;Organic Reaction Mechanisms · 2014;2018-01-05
5. Quinquevalent phosphorus acids;Organophosphorus Chemistry;2016
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