A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The reaction involves stereoselective trapping of diazo-derived rhodium carbenoids with gold-activated alkynols for the installation of spiro cores. The reaction has proven general with a range of readily accessible homopropargylic alcohols and diazo carbonyls to provide functionalized spiroether cores of bioactive scaffolds such as spirobarbiturates, spirooxindoles, and pseurotin natural products
Stereoselective construction of spiro-fused tricyclic compounds from enynes having a tethered imine ...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
Within the field of drug design, there is a great interest in the development of synthetic libraries...
A novel relay Rh (II)/cobaloxime (III) dual catalysis strategy has been developed for the stereosele...
In the recent decade there has been a shift in drug development to favor planar, aromatic small mole...
The reaction of cyclic diazoamides with aryl aldehydes catalyzed by rhodium(II) acetate leads to int...
The reaction of cyclic diazoamides with aryl aldehydes catalyzed by rhodium(II) acetate leads to int...
We have demonstrated a simple and an efficient method for the synthesis of spirocycles starting with...
Stereoselective construction of spiro-fused tricyclic compounds from enynes having a tethered imine ...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
A convergent approach for the stereoselective synthesis of diverse spiroethers is described. The rea...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
International audienceThe synthetic utility of γ-alkylidenebutenolides is demonstrated as highly com...
Within the field of drug design, there is a great interest in the development of synthetic libraries...
A novel relay Rh (II)/cobaloxime (III) dual catalysis strategy has been developed for the stereosele...
In the recent decade there has been a shift in drug development to favor planar, aromatic small mole...
The reaction of cyclic diazoamides with aryl aldehydes catalyzed by rhodium(II) acetate leads to int...
The reaction of cyclic diazoamides with aryl aldehydes catalyzed by rhodium(II) acetate leads to int...
We have demonstrated a simple and an efficient method for the synthesis of spirocycles starting with...
Stereoselective construction of spiro-fused tricyclic compounds from enynes having a tethered imine ...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...
Rh(III)-catalyzed [3 + 2] annulation of cyclic <i>N</i>-sulfonyl or <i>N</i>-acyl ketimines with ac...