Archive for February, 2013
Posted by naturalproductman on February 27, 2013
Hao Xu and co-workers at Georgia State University have reported in JACS on an iron catalyzed aminohydroxylation reaction.

JACS paper
Posted in Cascade Reactions, Iron, Methodology, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 27, 2013
Young Ho Rhee and co-workers from Pohang University of Science and Technology have reported in Org Lett on a gold catalyzed coupling of an alkynoate and allylic ether.

OL paper
Posted in Cascade Reactions, Gold, Mechanistic, Methodology, Sigmatropic Rearrangements, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 27, 2013
Samir Zard and colleague at CNRS have reported in JACS on a radical cascade C-C bond forming reaction.

JACS paper
Posted in Cascade Reactions, Methodology, Radical Chemistry | Leave a Comment »
Posted by naturalproductman on February 26, 2013
Jieping Zhu and co-workers from CNRS have reported in Tetrahedron on an aminopalladation reaction.

Tetrahedron paper
Posted in Cascade Reactions, Methodology, Palladium, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 26, 2013
Debabrata Maiti and co-workers from IIT Bombay have reported in JACS on a way to introduce nitro groups into olefins using TEMPO.

JACS paper
Posted in Methodology, Radical Chemistry, Silver, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 22, 2013
Hayamitsu Adachi and co-workers from BIKAKEN have reported in JNP on a novel VEGF receptor tyrosine kinase inhibitor from bacteria. The only problem I see with this compound – from a toxicologist’s perspective – is that this is a quinone, and thus a very reactive electrophile. If this kind of functional group is used as a drug, who knows what other things it will react with in the body – be it DNA, proteins, etc…

JNP paper
Posted in Alkaloids, Enzymes, Protein Targets, Proteins | Leave a Comment »
Posted by naturalproductman on February 22, 2013
Tomas Martin and co-workers from the Universidad de La Laguna in Spain have reported in ACIE on the synthesis of teurilene through an epoxide ring opening cascade.

ACIE paper
Posted in Cascade Reactions, Methodology, Tetrahydrofuran, Total Synthesis | Leave a Comment »
Posted by naturalproductman on February 21, 2013
C-H bond activation is popular because you can convert alkanes into alcohols – looks like a desaturase reaction where alkanes turn into alkenes is going to be up and coming in popularity soon. Pedro Perez and co-workers at CIQSO in Spain have reported in JACS on a copper catalyst that converted alkanes to alkenes.
JACS paper
Posted in C-H activation, Cascade Reactions, Copper, Dehydrogenation, Methodology, Transition Metal | Leave a Comment »
Posted by naturalproductman on February 21, 2013
John Chisholm and co-workers from Syracuse University have reported in Tetrahderon Letters on an intramolecular approach towards maeocrystal V.

TL paper
Posted in Cycloaddition, Diels-Alder, Methodology, Named Reactions, Pericyclic reactions | Leave a Comment »
Posted by naturalproductman on February 20, 2013
Seth Herzon and co-workers have published in ACIE on the synthesis of acutimine.

ACIE paper
Posted in Alkaloids, Total Synthesis | Leave a Comment »