Stereoselective synthesis of enantiomerically pure d-threo-PDMP; manipulation of a core 2,3-diamino alcohol unit
摘要:
The C(3)-N bond of various non-activated enantiomerically pure aziridine-2-methanols was regioselectively cleaved by nitrogen nucleophiles to provide a variety of beta-aminoalanine derivatives in high yields. (C) 2000 Published by Elsevier Science Ltd.
Efficient Syntheses of (<i>1R,2R</i>)- and (<i>1S,2S</i>)-2-Amino-1-alkyl(or aryl)-1,3-propanediols by Regioselective Ring Opening of Aziridine-2-methanols
作者:Soo-Kyung Choi、Jin-Soo Lee、Jung-Ho Kim、Won Koo Lee
DOI:10.1021/jo961168z
日期:1997.2.1
Stereoselective synthesis of enantiomerically pure d-threo-PDMP; manipulation of a core 2,3-diamino alcohol unit
作者:Seong-Ho Shin、Eun Young Han、Chan Sun Park、Won Koo Lee、Hyun-Joon Ha
DOI:10.1016/s0957-4166(00)00319-0
日期:2000.8
The C(3)-N bond of various non-activated enantiomerically pure aziridine-2-methanols was regioselectively cleaved by nitrogen nucleophiles to provide a variety of beta-aminoalanine derivatives in high yields. (C) 2000 Published by Elsevier Science Ltd.
Highly diastereoselective reduction of enantiomerically pure aziridino ketones
作者:Bong Chan Kim、Won Koo Lee
DOI:10.1016/0040-4020(96)00703-x
日期:1996.9
Various enantiomerically pure aziridino ketones were prepared from the corresponding secondary alcohols by Swern oxidation. Those configurationally stable α-amino ketones were stereoselectively reduced by L-Selectride® to provide the corresponding alcohol with high diastereoselectivities and chemical yields.