ABSTRACT
Direct enantioselective Mannich reactions of α-azido cyclic ketones with aldimines are realized through chiral phosphoric acid catalysis, which generate chiral azides possessing an α-quanternary stereocenter with complete regioselectivities and high diastereoselectivities and enantioselectivities.
ABSTRACT
The regioselective and enantioselective synthesis of ß-indolyl cyclopentenamides, a versatile chiral building block, by asymmetric addition of indoles to α,ß-unsaturated iminium intermediates has been achieved through chiral anion catalysis. Key to the success of this methodology is the generation of a chiral anion-paired ketone-type α,ß-unsaturated iminium intermediate from α-hydroxy enamides. Preliminary mechanistic studies and DFT calculations are consistent with a mechanism involving multiple, concurrent pathways for isomerization of the initially formed azaallylcation into the key α,ß-unsaturated iminium intermediate, all mediated by the phosphoric acid catalyst.