Kim, Dwight D. Lee, Suk Joong Beak, Peter Asymmetric Lithiation−Substitution Sequences of Substituted Allylamines (−)-Sparteine-mediated asymmetric lithiation−substitution sequences of 2- and 3-substituted <i>N</i>-(Boc)-<i>N</i>-(<i>p</i>-methoxyphenyl) allylic amines with electrophiles have been investigated. Asymmetric lithiation−substitutions of <i>N</i>-(Boc)-<i>N</i>-(<i>p</i>-methoxyphenyl) allylic amines <b>11</b>, <b>12</b>,<b> 13</b>,<b> 14</b>, and <b>15</b> provide highly enantioenriched enecarbamates in good yields. Further transformations to give aldehydes, acids, ketones, and a Diels−Alder adduct are reported. The 1,4-addition products from reactions of the lithiated allylic amines from <b>14 </b>and<b> 15</b> with conjugated activated alkenes gives enecarbamates with two and three stereogenic centers in good yields with high diastereomeric and enantiomeric ratios. Synthetic transformation of these products by acid hydrolysis and subsequent cyclization provide stereoselective access to bicyclic compounds containing four and five stereogenic centers with high diastereoselectivity and enantioselectivity. It is suggested that allyllithium complexes generated by asymmetric deprotonation react with most electrophiles with inversion of configuration. Asymmetric;enecarbamate;transformation;lithiation;electrophile;lithiated allylic amines;stereogenic centers;allylic amines 11;methoxyphenyl;Boc;yield;acid 2005-07-08
    https://acs.figshare.com/articles/dataset/Asymmetric_Lithiation_Substitution_Sequences_of_Substituted_Allylamines/3278098
10.1021/jo047752m.s010