Stereoselective Total Synthesis of the Natural Oxylipin (6R,7E,9R,10S)-6,9,10-Trihydroxyoctadec-7-enoic Acid
Author:
Publisher
Wiley
Subject
Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Drug Discovery,Biochemistry,Catalysis
Reference26 articles.
1. Oxylipins from Dracontium loretense
2. Stereoselective total synthesis of both (6R,9R,10S,7E)- and (6S,9R,10S,7E)-epimers of oxylipin (9R,10S,7E)-6,9,10-trihydroxyoctadec-7-enoic acid
3. First asymmetric synthesis of the oxylipin, (6S,9R,10S)-6,9,10-trihydroxyoctadeca-7E-enoic acid
4. Stereoselective Total Synthesis of Oxylipins: (6S,7E,9R,10S)-6,9,10-Trihydroxyoctadec-7-enoic Acid and (6Z,8R,9R,10S)-8,9,10-Trihydroxyoctadec-6-enoic Acid
5. Recent Developments in Olefin Cross-Metathesis
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3. Three-step synthesis of oxylipins from D. loretense;Tetrahedron Letters;2019-07
4. The chemistry of the carbon-transition metal double and triple bond: Annual survey covering the year 2015;Coordination Chemistry Reviews;2016-12
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