Stereoselective Synthesis of N‐Propargyl Alkynes and Axial Chiral N‐Allenes with Epimeric Pyrroloimidazolone Auxiliaries

Abstract An N ‐propargyl pyrroloimidazolone with syn stereochemistry derived from L‐proline serves as a starting material for the diastereoselective synthesis (>95:5 dr) of propargyl alkynes or allenamides by direct quench of its lithiated intermediate with alkylating agents or aldehydes/ketones, respectively. Use of the epimeric anti pyrroloimidazolone starting material results in reversal of stereochemistry at the propargyl position in the products, without the need to prepare a separate substrate from D‐proline. Lithiation of the syn pyrroloimidazolone and quench with prochiral benzaldehydes without prior transmetalation gives allenamides with crystallographically verified atypical stereochemistry of the benzylic alcohol in >95:5 dr. The epimeric series of benzylic alcohols may also be obtained in >95:5 dr by employing transmetalation with chlorotitanium triisopropoxide prior to aldehyde quench. Density Functional Theory (DFT) computational studies provide a rationale for the change in benzylic alcohol stereochemistry by virtue of differing stereofacial attack in 6,5‐bicyclic (Li) or 6‐membered (Ti) transition states. magnified image