Jiong Yang and co-workers from Texas A&M have reported in JOC on a transannular Michael reaction.

Posted by naturalproductman on October 3, 2012
Jiong Yang and co-workers from Texas A&M have reported in JOC on a transannular Michael reaction.

Posted in Cascade Reactions, Methodology, Michael, Named Reactions, Ring forming, Transannular | Leave a Comment »
Posted by naturalproductman on February 23, 2012
Aurelio Csaky and co-workers from Universidad have reported in Organic Letters on an interesting way to form substituted tetrahydropyran rings.

Posted in Cascade Reactions, Methodology, Michael, Named Reactions | Leave a Comment »
Posted by naturalproductman on January 25, 2012
Emmanuel Roulland and colleague at CNRS have reported in the European JOC on their progress towards landomycinone.

Posted in Cascade Reactions, Methodology, Michael, Named Reactions, Polyketides | Leave a Comment »
Posted by naturalproductman on December 19, 2011
Hongbin Zhang and co-workers at Yunnan University have reported in ACIEE on their synthesis of stenine.

Posted in Alkaloids, Cascade Reactions, Conjugate Additions, Methodology, Michael, Named Reactions | Leave a Comment »
Posted by naturalproductman on November 21, 2011
Richard Silverman and co-workers at Northwestern have reported in JACS on celastrol as a Michael acceptor.
Posted in Chemical Biology, Methodology, Michael, Named Reactions | Leave a Comment »
Posted by naturalproductman on November 21, 2011
Gerald Pattenden and colleague at the University of Nottingham have reported in Tetrahedron on the synthesis of ineleganolide via a Michael reaction.
Posted in Cascade Reactions, Methodology, Michael, Named Reactions, Ring forming, Transannular | Leave a Comment »
Posted by naturalproductman on September 30, 2011
Seirjiro Matsubara and colleague at Kyoto University have reported in JACS on an organocatalytic oxy-Michael reaction.

Posted in Asymmetric, Conjugate Additions, Methodology, Michael, Named Reactions, Organocatalytic | Leave a Comment »
Posted by naturalproductman on September 26, 2011
Larry Overman and colleague have reported in JACS on a total synthesis of aplyviolene. Surprisingly, the bromide in the alpha-bromo enone Michael acceptor substrate did not get displaced.

Posted in Asymmetric, Cascade Reactions, Conjugate Additions, Diterpene, Methodology, Michael, Named Reactions, Total Synthesis | Leave a Comment »
Posted by naturalproductman on August 29, 2011
Xiaoyu Wu and co-workers at Shanghai University have reported in Chemistry a European Journal on a reaction that involves two named reaction using an indole tethered with a primary amine and an alkynoate as the subtrates.

Posted in Cascade Reactions, Indoles, Indolizidines, Methodology, Michael, Named Reactions, Organocatalytic, Pictet-Spengler | Leave a Comment »