Catalytic Enantioselective Synthesis of the Partially Reduced Tricyclic Pyrrolo3,2-c quinoline Core Structure of the Martinella Alkaloids

摘要

abstract_textpA catalytic enantioselective synthesis of the hexahydropyrrolo 3,2-c quinoline core structure found in the Martinella alkaloids, martinelline and martinellic acid, is described. The synthesis is completed without the use of any chiral building blocks or chiral auxiliaries. The key steps in our synthesis constituted a Sp2-Sp3 Suzuki-Miyaura cross-coupling reaction between a triflate and an N-protected beta-aminoethyl boron species to provide a 1,2-dihydroquinoline carrying a N-protected b-aminoethyl group in the 3-position, Sharpless asymmetric dihydroxylation of the 1,2-dihydroquinoline derived from the Suzuki-Miyaura cross-coupling reaction, and an acid promoted intramolecular diastereoselective amido cyclisation with the aid of a neighbouring acetoxy group to provide the tricyclic architecture of martinelline and martinellic acid. Our catalytic enantioselective synthesis provided the hexahydropyrrolo3,2-c quinoline core structure of the Martinella alkaloids in 75 ee./p/abstract_text