Asymmetric synthesis of two new conformationally constrained lysine derivatives

The asymmetric synthesis of the conformationally constrained l- and d-lysine derivatives methyl (1S,8S)-1-amino-8-tert-butoxycarbonylamino-1,2,3,4,5,6,7,8-octahydroanthracene-1-carboxylate () and methyl (1R,8S)-1-amino-8-tert-butoxycarbonylamino-1,2,3,4,5,6,7,8-octahydroanthracene-1-carboxylate (), respectively are described. Application of the Bucherer hydantoin synthesis to the carbonyl group of 2′,3′,4′,5′,6′,7′-hexahydrospiro[1,3-ethylenedithiole-2,1′-anthracen]-8′-one (), which was prepared from 1,8-dichloroanthraquinone () in nine steps and the deprotection of the masked second ketone of yields rac-21. The latter is the precursor for a novel asymmetric reductive amination protocol using (R)-phenylglycinol as a chiral amino auxiliary and NaBH(OAc)3 as a reducing agent. Using this procedure, the asymmetric reductive amination of α-tetralone derivatives and indanone proceeds with >95% de. Lower diastereomeric excesses are observed for benzosuberone (16.7% de) and acetophenone (27.3% de). rac-21 gave (38% yield) and (44.5% yield) with greater than 52 and 78% de, respectively. Cleavage of the amino auxiliary of and of with lead(IV) tetraacetate and hydrolysis of the hydantoin ring yields the unprotected analogs of and . The latter are transformed into the selectively protected target molecules and through standard protection procedures. The overall yield of the 17- and 18-step synthesis starting from was 0.3% yield for each constrained lysine derivative.