Development of the Ireland−Claisen Rearrangement of Alkoxy- and Aryloxy-Substituted Allyl Glycinates
作者:James P. Tellam、David R. Carbery
DOI:10.1021/jo1017124
日期:2010.11.19
The Ireland−Claisenrearrangement of 3-alkoxy- and 3-aryloxy-substituted allyl glycinates is presented. This [3,3]-sigmatropic rearrangement route offers direct access to syn β-alkoxy and β-aryloxy α-amino acid systems. In particular, N,N-diboc glycine esters rearrange with excellent diastereoselectivities (dr > 25:1). The synthesis of substrates, rearrangement optimization, and a discussion of stereoselection
Propargyl amide precursor to 1-propargyl-2,4-dioxoimidazolidine
申请人:Sumitomo Chemical Company, Limited
公开号:US04827020A1
公开(公告)日:1989-05-02
1-propargyl-2,4-dioxoimidazolidine is a very useful intermediate for synthesizing insecticidal and acaricidal compounds of pyrethroid type. Here are disclosed a method for producing 1-propargyl-2,4-dioxoimidazolidine, the starting material compounds thereof and a method for producing said starting material compounds. According to the present invention, said useful intermediate can be easily produced than before.