Steven Ley and co-workers have reported in ACIE on the synthesis of callipeltoside.
Archive for the ‘Yamaguchi macrolactonization’ Category
Callipeltoside synthesis
Posted by naturalproductman on August 23, 2012
Posted in Macrolides, Methodology, Named Reactions, Yamaguchi macrolactonization | Leave a Comment »
Amphidinolide F synthesis
Posted by naturalproductman on July 5, 2012
Posted in Cascade Reactions, Methodology, Named Reactions, Silver, Transition Metal, Vedejs olefination, Yamaguchi macrolactonization | Leave a Comment »
Syntheses of Peloruside
Posted by naturalproductman on July 20, 2010
The Jacobsen and Hoye groups have recently independently published on the synthesis of peloruside. Jacobsen et al took advantage of his enantioselective epoxide opening reaction while Hoye’s group used a relay ring closing metathesis to form the pyran moiety found in peloruside.
Posted in Metathesis, Methodology, Named Reactions, Polyketides, Total Synthesis, Yamaguchi macrolactonization | Leave a Comment »
Exiguolide Synthesis
Posted by naturalproductman on January 12, 2010
Exiguolide, a macrolide that specifically inhibits gamete fertilization of sea urchins but not the embryogenesis of the fertilized egg, was synthesized by Haruhiko Fuwa and co-workers at Tohoku University.
Posted in cross coupling, Julia-Kocienski, Macrocycles, Macrolides, Methodology, Polyenes, Suzuki-Miyaura, Transition Metal, Yamaguchi macrolactonization | Leave a Comment »
