International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and related alkenes occurs without complications from fragmentation or hydrogen atom abstraction and delivers a vast array of highly functional geminal bis(boronates). The ability to assemble geminal bis(boronates) bearing polar functional groups not readily obtained through existing methods is particularly noteworthy. This approach also opens up access to geminal bis(boronyl) cyclopropanes and geminal bis(boronyl) tetrahydroquinolines
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
The inability of the sp<sup>3</sup> boron in MIDA boronates to stabilize an adjacent radical makes p...
International audienceA modular approach to highly functional acyl (MIDA)boronates is described. It ...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
The inability of the sp<sup>3</sup> boron in MIDA boronates to stabilize an adjacent radical makes p...
International audienceA modular approach to highly functional acyl (MIDA)boronates is described. It ...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceThe radical addition of dithiocarbonates to 1,1-bis(boronyl)-3-butene and rela...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceA modular, stereoselective route to trisubstituted (Z)-alkenyl (MIDA)boronates...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
International audienceThe inability of the sp(3) boron in MIDA boronates to stabilize an adjacent ra...
The inability of the sp<sup>3</sup> boron in MIDA boronates to stabilize an adjacent radical makes p...
International audienceA modular approach to highly functional acyl (MIDA)boronates is described. It ...