Synthesis of the C28 through C38 segment of okadaic acid using vinylogous urethane aldol chemistry: Part IV
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference28 articles.
1. Okadaic acid, a cytotoxic polyether from two marine sponges of the genus Halichondria
2. Synthesis of a marine polyether toxin, okadaic acid [1] — strategy and synthesis of segment a
3. Synthesis of a marine polyether toxin, okadaic acid (2) — synthesis of segment b
4. Synthesis of a marine polyether toxin, okadaic acid (3) — synthesis of segment c
5. Synthesis of a marine polyether toxin, okadaic acid [4]p1 -- total synthesis
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1. Electrochemical and photochemical approaches for the synthesis of the C28–C38 fragment of okadaic acid;Tetrahedron;2019-04
2. Diastereoselective Total Synthesis of Raputindole A;Organic Letters;2018-08-28
3. anti-Selective aldol reactions of chiral alcohol substituted γ-benzyloxyl vinylogous urethanes and the synthesis of 3-benzyloxyl-4-hydroxylalkan-2-ones;Tetrahedron: Asymmetry;2017-11
4. Dinophyceae (Dinoflagellates);Encyclopedia of Marine Natural Products;2014-08-07
5. The Vinylogous Aldol and Related Addition Reactions: Ten Years of Progress;Chemical Reviews;2011-03-24
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