Yen-Ho Chu and co-workers at the National Chung Cheng University in Taiwan have published in Organic Letters on a synthesis of luotonin. This compound has in vitro activity against murine leukemia P-388 cell line with an IC50 value of 6.3 micromolar.
Archive for the ‘Ytterbium’ Category
It’s all in one pot!
Posted by naturalproductman on January 26, 2011
Posted in Alkaloids, Cancer, Cascade Reactions, leukemia, Methodology, One pot, Transition Metal, Ytterbium | Leave a Comment »
Zn/Yb-Mediated Conia-Ene Reaction
Posted by naturalproductman on August 17, 2010
Jin-Heng Li and co-workers from Hunan Normal University have published in Synthesis on a Conia-ene reaction using Yb and Zn. This reaction is catalytic in zinc but stoichiometric in ytterbium. When a terminal alkyne is used, the cyclization is in the exo-dig mode, but when an internal alkyne is used, the cyclization is in the endo-dig mode.
Posted in Cascade Reactions, Conia-Ene, Methodology, Named Reactions, Ring forming, Transition Metal, Ytterbium, Zinc | Leave a Comment »
Two Step Access to Substituted Amino-pyrroles
Posted by naturalproductman on June 27, 2010
Takeo Konakahara and co-workers at the Tokyo University of Science have reported in the European Journal of Organic Chemistry on a multicomponent approach to synthesize aza dienes and followed by a ytterbium catalyzed [4+2] reaction between the azadiene and TMS-cyanide.
Posted in Cascade Reactions, Methodology, Multi-Component Coupling, Transition Metal, Ytterbium | Leave a Comment »
Synthesis of Platyphyllide
Posted by naturalproductman on May 11, 2010
Atsushi Nishida and co-workers from Chiba University have recently reported in JOC on the asymmetric synthesis of platyphyllide with the key reaction being an asymmetric Diels-Alder reaction.
Posted in Asymmetric, Cascade Reactions, Cycloaddition, Diels-Alder, Ito-Saegusa oxidation, Methodology, Named Reactions, Palladium, Pericyclic reactions, Transition Metal, Ytterbium | Leave a Comment »
Propargyl/Allyl/Vinyl Silanes
Posted by naturalproductman on May 8, 2010
Marek Chmielewski and co-workers at the Institute of Organic Chemistry of the Polish Academy of Sciences have recently reported in Tetrahedron on some intramolecular cyclization reactions generating an acyliminium ion in the presence of either a propargyl, allyl, or vinyl silane.
Posted in Cascade Reactions, Methodology, Ring forming, Titanium, Transition Metal, Ytterbium | Leave a Comment »