Hidetoshi Yamada and co-workers at Kwansei Gakuin University have reported in JOC on a structural reassignment concluding that roxbin B is cuspinin.

Posted by naturalproductman on May 21, 2013
Hidetoshi Yamada and co-workers at Kwansei Gakuin University have reported in JOC on a structural reassignment concluding that roxbin B is cuspinin.

Posted in Glycosides, Methodology, Structural Reassignment, Total Synthesis | Leave a Comment »
Posted by naturalproductman on May 17, 2013
Posted in Macrolides, Methodology, Total Synthesis | Leave a Comment »
Posted by naturalproductman on May 17, 2013
Keisuke Suzuki and co-workers at Tokyo Institute of Technology have reported in ACIE on the synthesis of

Posted in Antibiotics, Methodology, Total Synthesis | Leave a Comment »
Posted by naturalproductman on May 17, 2013
Brian Stoltz and co-workers have reported in ACIE on the syntheses of transtaganolides through an Ireland-Claisen rearrangement/Diels-Alder cascade.

Posted in Asymmetric, Cascade Reactions, Claisen rearrangement, Diels-Alder, Methodology, Named Reactions, Sesquiterpenes, Total Synthesis | Leave a Comment »
Posted by naturalproductman on May 10, 2013
Antonio Echavarran and co-workers at ICIQ have reported in ACIE on a synthesis of schisanwilsonene A.

Posted in Methodology, Sesterterpenes, Seven-Membered Rings, Total Synthesis | Leave a Comment »
Posted by naturalproductman on May 8, 2013
Ian Paterson and co-workers from the University of Cambridge have reported in ACIE on the synthesis of rhizopodin.

Posted in Macrolides, Methodology, Oxazoles, Total Synthesis | Leave a Comment »
Posted by naturalproductman on April 18, 2013
Mark Lautens and co-workers at the University of Toronto have reported in ACIE on the synthesis of linoxepin.

Posted in Aromatic, Polyketides, Total Synthesis | Leave a Comment »
Posted by naturalproductman on April 18, 2013
Erick Carreira and co-workers have reported in ACIE on the synthesis of some pro-inflammatory compounds, which look like good Michael acceptors.

Posted in Biological activity, Total Synthesis | Leave a Comment »
Posted by naturalproductman on April 18, 2013
Masayuki Inoue and co-workers from University of Tokyo have reported in ACIE on a synthesis of 19-hydroxysarmentogenin.

Posted in Methodology, Steroids, Total Synthesis | Leave a Comment »