Tatyana Makarieva and co-workers from the Russian Academy of Sciences have reported in Tetrahedron Letters on the isolation of pulchranin A.

Posted by naturalproductman on January 31, 2013
Tatyana Makarieva and co-workers from the Russian Academy of Sciences have reported in Tetrahedron Letters on the isolation of pulchranin A.

Posted in Alkaloids | Leave a Comment »
Posted by naturalproductman on January 31, 2013
Shuji Yamashita and co-workers from Tohoku University have reported in Tetrahedron Letters on a C-H amination of the C12-position of steroids.

Posted in C-H activation, Methodology, Steroids | Leave a Comment »
Posted by naturalproductman on January 31, 2013
James White and co-workers have reported in Organic Letters on the synthesis of huperzine A.

Posted in Alkaloids, Asymmetric, Methodology, Named Reactions, Prins, Total Synthesis | Leave a Comment »
Posted by naturalproductman on January 31, 2013
Jun’ichi Kobayashi and co-workers from Hokkaido University have reported in Organic Letters on the isolation of zamamiphidin A.

Posted in Alkaloids | Leave a Comment »
Posted by naturalproductman on January 31, 2013
Zhigang She and co-workers from Sun-Yat Sen University have reported in Organic Letters on the isolation of asperterpenoid A, which had an IC50 value of 2.2 micromolar against Mycobacterium tuberculosis protein tyrosine phosphatase B (mPTPB).

Posted in Protein Targets, protein tyrosine phosphatase 1B (PTP1B), Terpenoids | Leave a Comment »
Posted by naturalproductman on January 31, 2013
Posted in Allenes, C2-Symmetric, Methodology, Organocatalytic | Leave a Comment »
Posted by naturalproductman on January 31, 2013
Norio Shibata and co-workers from the Nagoya Institute of Technology have reported in ACIE on an enantioselective epoxidation reaction using a cinchona alkaloid derived catalyst.

Posted in Asymmetric, Epoxidation, Methodology, Organocatalytic | Leave a Comment »
Posted by naturalproductman on January 23, 2013
Eric Jacobsen and co-workers have published in JACS on an aza-Diels-Alder. I didn’t know the N. stood for Niels.
Posted in Cascade Reactions, Diels-Alder, Methodology, Named Reactions | Leave a Comment »