A highly efficient synthesis of (S)-(+)-N-Boc-coniine using ring-closing olefin metathesis (RCM)
暂无分享,去创建一个
[1] M. Mckervey,et al. Convenient in Situ Synthesis of Nonracemic N-protected β-Amino Aldehydes from β-Amino Acids. Applications in Wittig Reactions and Heterocycle Synthesis , 1999 .
[2] David R. Williams,et al. Total Synthesis of (+)-Amphidinolide J , 1998 .
[3] S. Buchwald,et al. Short Enantioselective Total Syntheses of the Piperidine Alkaloids (S)-Coniine and (2R,6R)-trans-Solenopsin A via Catalytic Asymmetric Imine Hydrosilylation. , 1998, The Journal of organic chemistry.
[4] Robert H. Grubbs,et al. Recent advances in olefin metathesis and its application in organic synthesis , 1998 .
[5] H. Schoemaker,et al. Ruthenium-catalyzed ring closing olefin metathesis of non-natural α-amino acids , 1997 .
[6] R. Grubbs,et al. The synthesis of nitrogen heterocycles via catalytic ring-closing metathesis of dienes , 1992 .
[7] S. Pelletier. Alkaloids: Chemical and Biological Perspectives , 1992, Alkaloids: Chemical and Biological Perspectives.
[8] H. Waldmann,et al. Organic Synthesis Highlights , 1990 .
[9] H. Kotsuki,et al. A novel carbon-carbon bond-forming reaction of triflates with copper(I)-catalyzed grignard reagents. A new concise and enantiospecific synthesis of (+)-exo-brevicomin, (5R,6S)-(-)-6-acetoxy-5-hexadecanolide, and L-factor , 1990 .