Total synthesis of rubrolide M and some of its unnatural congeners
Author:
Publisher
Elsevier BV
Subject
Organic Chemistry,Drug Discovery,Biochemistry
Reference10 articles.
1. New Rubrolides from the Ascidian Synoicum blochmanni
2. Selective synthesis of (Z)-4-aryl-5-[1-(aryl)methylidene]-3-bromo-2(5H)-furanones
3. For reviews on the synthesis of stereodefined 5-ylidene-2(5H)-furanones, see: (a) Negishi, E.-I.; Kotora, M. Tetrahedron 1997, 53, 6707–6738; (b) Brückner, R. Curr. Org. Chem. 2001, 5, 679–718. For the β-elimination route to stereodefined 5-ylidene-2(5H)-furanones, see: Brückner, R. Chem. Commun. 2001, 141–152.
4. Facile access to 4-aryl-2(5H)-furanones by Suzuki cross coupling: Efficient synthesis of rubrolides C and E
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