Synthesis of chiral methyl-branched linear pheromones starting from (+)-aromadendrene. Part 7
作者:Yvonne M.A.W Lamers、Ghena Rusu、Joannes B.P.A Wijnberg、Aede de Groot
DOI:10.1016/j.tet.2003.09.085
日期:2003.11
ate (4), a linear methyl-branched intermediate with its chiral center at C7, and with two different functional groups at the ends of the chain, has been synthesized from (+)-aromadendrene in nine steps. A Baeyer–Villiger oxidation and a Grob fragmentation are the key reactions in this transformation. Intermediate 4 has been applied in the synthesis of three linear methyl-branched pheromones, (i) (