Myrrhanol A
Posted by naturalproductman on July 6, 2009
Alejandro Barrero at the University of Granada in Spain and co-workers have recently published in JOC on the synthesis of an anti-inflammatory agent, myrrhanol A. A key step in the synthesis was the reaction they used to make the 6,6-scaffold of the molecule, which involved a cascade titanium mediated bis-olefin epoxide opening cyclization.

This entry was posted on July 6, 2009 at 6:38 am and is filed under Cascade Reactions, cross coupling, Methodology, Polypodanes, Ring forming, Transition Metal, Triterpenes. You can follow any responses to this entry through the RSS 2.0 feed. You can leave a response, or trackback from your own site.
Edinburgher said
Hey man, Barrero didnt set up the whole Uni and then name it after himself.
Furthermore, there is a long tradition of Ti(III)-chemistry in that Uni with titanocenes, some of it really interesting. In particular there is an Angewandte of 2006 (as far as I remember), quite cool.
naturalproductman said
Woops thanks for the correction! And thanks for the reference.