156714-70-4Relevant academic research and scientific papers
Asymmetric synthesis of (2R,4R,5S)-tetrahydropseudodistomin and stereoisomers by cycloaddition of nitrone to vinylglycinol
Kiguchi, Toshiko,Ikai, Miho,Shirakawa, Mitsuko,Fujimoto, Kuniko,Ninomiya, Ichiya,Naito, Takeaki
, p. 893 - 899 (2007/10/03)
Cycloaddition of the nitrone, derived from tetradecanal, to vinylglycinol provides an asymmetric synthesis of both (2R,4R,5S)-tetrahydropseudodistomin and all the stereoisomers of the racemic tetrahydropseudodistomins.
Cycloaddition of a Nitrone to 2-Aminobut-3-en-1-ol for Large-scale Preparation of 3-Aminopiperidin-4-ols: A New Asymmetric Synthesis of (2R,4R,5S)-Tetrahydropseudodistomin
Naito, Takeaki,Ikai, Miho,Shirakawa, Mitsuko,Fujimoto, Kuniko,Ninomiya, Ichiya,Kiguchi, Toshiko
, p. 773 - 776 (2007/10/02)
Cycloaddition of the nitrone, derived from tetradecanal, to 2-aminobut-3-en-1-ol provides a practical asymmetric synthesis of both (2R,4R,5S)-tetrahydropseudodistomin and all the stereoisomers of racemic tetrahydropseudodistomin.
